GMP Audit Services

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GMP (Good Manufacturing Practices) is set of practices for manufacturing business. GMP standard was originated in Europe & has become very popular worldwide in due course of time. There are different GMP standards developed by different governments & organisations but all are similar. These all GMP standards addresses some common issues which are : Sanitation, Hygiene & maintenance.
CDG is a world leader in compliance certification. We provide gmp certification services in India & overseas. Our GMP compliance certification is recognised worldwide. Good manufacturing practice" or "GMP" is required being adapted in the manufacturing of pharmaceuticals or drugs, active pharmaceutical ingredients, diagnostics, foods and medical devices. GMPs are guidance that outlines the aspects of production and testing that can impact the quality of a product. Many countries have regulatory requirements that Pharmaceutical and Medical Device companies must follow GMP procedures, and have created their own GMP guidelines that correspond with their legislation.
CDG provides tailored solutions to all kinds of GMP compliance issues. With extensive experience of the GMP certification process, our regulatory experts will provide all the support you need to achieve GMP excellence.

GMP Gap analysis audit:

• CDG's auditor will visit your site and perform an audit to determine where you need to improve your processes, documentation, and operations. CDG have experienced people able to perform GMP Audit Readiness/GMP GAP assessments for your facility against GMP requirements. CDG also be able to offer assistance in correcting any deficiencies found.
• GMP compliance is viewed today as an essential baseline of food safety for food packers, processors manufacturers, and greenhouses.
• GMP audits are increasingly required by retailers as proof that you take food safety seriously. Independent GMP verification confirms your operation's food safety practices and processes. Many countries follow the guidelines provide by WHO. 
• Food and Drugs Control Authority India follows WHO guidelines. WHO GMP certification is a requirement and well accepted in most of the countries across Asia, Africa, CIS and Latin America

Other information:

• WHO Good manufacturing practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product. The main risks are: unexpected contamination of products, causing damage to health or even death; incorrect labels on containers, which could mean that patients receive the wrong medicine; insufficient or too much active ingredient, resulting in ineffective treatment or adverse effects.
• WHO GMP covers all aspects of production; from the starting materials, premises and equipment to the training and personal hygiene of staff. Detailed, written procedures are essential for each process that could affect the quality of the finished product. There must be systems to provide documented proof that correct procedures are consistently followed at each step in the manufacturing process - every time a product is made.

Additional Information:

• Item Code: GMP

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A good manufacturing practice (GMP) is a production and testing practice that helps to ensure a quality product. Many countries have legislated that pharmaceutical and medical device companies must follow GMP procedures, and have created their own GMP guidelines that correspond with their legislation. Basic concepts of all of these guidelines remain more or less similar to the ultimate goals of safeguarding the health of the patient as well as producing good quality medicine, medical devices or active pharmaceutical products. Good Manufacturing Practices (GMP) certification from CDG certification ltd. ensures the integrity of your food manufacturing process as well as your compliance with food safety regulations. Assurance of the safety and quality of food is an important consideration for consumers today. A GMP is an important enhancement to your food safety management system, which increases your customers’ confidence in your commitment to trading and producing safe, high quality food.

A Good Manufacturing Practices (GMP) certification scheme provides independent verification and certification that the basic manufacturing practices. GMP regulations address issues including record keeping, personnel qualifications, sanitation, cleanliness, equipment verification, process validation, and complaint handling. Most GMP requirements are very general and open-ended, allowing each manufacturer to decide individually how to best implement the necessary controls. This provides much flexibility, but also requires that the manufacturer interpret the requirements in a manner which makes sense for each individual business. Good manufacturing practice (GMP) is part of a quality system covering the manufacture and testing of active pharmaceutical ingredients, diagnostics, foods, pharmaceutical products and medical devices.

GMP Certification confirms the products identity, composition, quality, purity and strength which they represent in the market. Under it, there is a set of guidelines that offer a system of procedures and documentation by which the confirmation of the products are given.
5 Key Components of Good Manufacturing Practices• Primary Materials and Products.• Premises.• People.• Procedures.• Processes.Qualified FDA GMP consultants can help your company plan, implement, and maintain systems to ensure GMP compliance. The good GMP consultants may recommend modern technologies and proven processes to achieve higher quality and more efficient processes.

What is the Procedure to get GMP Certification?Application. This is the initial step to get the GMP certification; the application covers some essential data of the organization.• Review of Application. • Analysis & Agreement.• Documentation Review.• Granting Of Certification.• Surveillance Audit.

CDG is one of the platforms which coordinate to fulfil all your legal and financial requirements and connect you to consistent professionals. 

Service Details:

GMP refers to the Good Manufacturing Practice Regulations. GMP certification is granted to manufacturing or service systems of organisations to certify that they engage with good manufacturing practices in their manufacturing or service processes, according to a Standard Code of Practice related to their business. Good manufacturing practice (GMP) is part of a quality system covering the manufacture and testing of active pharmaceutical ingredients, diagnostics, foods, pharmaceutical products and medical devices.

GMP Certification confirms the products identity, composition, quality, purity and strength which they represent in the market. Under it, there is a set of guidelines that offer a system of procedures and documentation by which the confirmation of the products are given. Good manufacturing practice (GMP) is that part of quality assurance which ensures that products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the marketing authorization. GMP is aimed primarily at diminishing the risks inherent in any pharmaceutical production, which may broadly be categorized in two groups; cross contamination/mix-ups and false labelling. Above all, manufacturers must not place patients at risk due to inadequate safety, quality or efficacy; for this reason, risk assessment has come to play an important role in WHO quality assurance guidelines.

Good manufacturing practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product. The main risks are: unexpected contamination of products, causing damage to health or even death; incorrect labels on containers, which could mean that patients receive the wrong medicine; insufficient or too much active ingredient, resulting in ineffective treatment or adverse effects. GMP covers all aspects of production; from the starting materials, premises and equipment to the training and personal hygiene of staff. Detailed, written procedures are essential for each process that could affect the quality of the finished product. There must be systems to provide documented proof that correct procedures are consistently followed at each step in the manufacturing process - every time a product is made. A Good Manufacturing Practices (GMP) certification scheme provides independent verification and certification that the basic manufacturing practices and prerequisites necessary for the implementation of an effective Hazard Analysis Critical Control Point (HACCP) food safety programme are being followed.

What are the 3 importance of GMP?Good Manufacturing Practices help ensure the proper design, monitoring, and control of manufacturing processes and facilities, while securing the identity, strength, and quality of their products. Other Details: • Flexible approach• Use advanced technologies• Crystal clear dealings• Timely executed Manufacturer’s Advantages One of the main advantages is that the manufacturer's quality systems and quality compliance have greatly improved. These gains were visible in the months coming up to GMP certification and continued in the years following certification. In the pharmaceutical sector, GMP is followed. MP refers to a system of rules, rules, and procedures that govern the processing of drug substances and products, medical equipment, medical product categories in vivo and in vitro, and food items.

Our motive is to keep up with the advancements and regulate the processes to produce superior quality medicines.
CDG provide  GMP certification Services in  India.

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What is GMP compliance?
CGMPs provide for systems that assure proper design, monitoring, and control of manufacturing processes and facilities. Adherence to the CGMP regulations assures the identity, strength, quality, and purity of drug products by requiring that manufacturers of medications adequately control manufacturing operations.

Principles of GMP Compliance Certificate:
1. Hygiene: Pharmaceutical manufacturing facility must maintain a clean and hygienic manufacturing area.
2. Controlled environmental conditions in order to prevent cross contamination of drug product from other drug or extraneous particulate matter which may render the drug product unsafe for human consumption.
3. Manufacturing processes are clearly defined and controlled. All critical processes are validated to ensure consistency and compliance with specifications.
4. Manufacturing processes are controlled, and any changes to the process are evaluated. Changes that have an impact on the quality of the drug are validated as necessary.
5. Instructions and procedures are written in clear and unambiguous language. (Good Documentation Practices)
6. Operators are trained to carry out and document procedures.
7. Records are made, manually or by instruments, during manufacture that demonstrate that all the steps required by the defined procedures and instructions were in fact taken and that the quantity and quality of the drug was as expected.Deviations are investigated and documented.
8. Records of manufacture (including distribution) that enable the complete history of a batch to be traced are retained in a comprehensible and accessible form.
9. The distribution of the drugs minimizes any risk to their quality.
10. A system is available for recalling any batch of drug from sale or supply.
11. Complaints about marketed drugs are examined, the causes of quality defects are investigated, and appropriate measures are taken with respect to the defective drugs and to prevent recurrence.

CDG offering a wide range of GMP Certification Services. Good manufacturing practice GMP is required being adopted in the manufacturing of pharmaceuticals or drugs, active pharmaceutical ingredients, diagnostics, foods and medical devices. GMPs are guidance that outlines the aspects of production and testing that can impact the quality of a product.


Other Details:• Timely executed• Exact manifestation of customer requirements• Highly flexible• Best quality inputs used

It is the responsibility of the organization to ensure that claims of conformity to GMP Certification with respect to health, safety, environmental protection is ensured.

Documents Required• Registration Certificate• Office Address Proof• Scope of the work• GST Certificate• Cancelled Cheque• Bills raised/Invoice paid• Basic KYC of Director/Partner/Prop.• Type of Products looking for GMP


CDG Certification Ltd. counted among the leading firms that are engaged in rendering services for ISO 9001 Certification Services.

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CDG-Our organization is a foremost name in the industry, engaged in offering a wide assortment of GMP Registration Services to our clients. CDG offered services are highly appreciated by clients for their low cost and accurate results. Also, these services are rendered by employing highly experienced team members. Further, these services are offered at very reasonable rates.


Other Details:Excellent results Timely executed Best quality inputs used Rendered as per customer requirement
Good Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product. Good manufacturing practices (GMP) are the practices required in order to conform to the guidelines recommended by agencies that control authorization and licensing for manufacture and sale of food, drug products, and active pharmaceutical products. These guidelines provide minimum requirements that a pharmaceutical or a food product manufacturer must meet to assure that the products are of high quality and do not pose any risk to the consumer or public.

A GMP is a system for ensuring that products are consistently produced and controlled according to quality standards. GMP covers all aspects of production from the starting materials, premises and equipment to the training and personal hygiene of staff. Detailed, written procedures are essential for each process that could affect the quality of the finished product.

CDG provides GMP certification services in India. GMP ensures best practices of hygeine & safety during manufacturing. CDG is a leading GMP compliance certification provider in India.

Benefits of GMP Certification• Empower certification holders to opt great creation,• Timely identify of manufactures and the management issues,• Compliance with important laws and guidelines,• Improve overall credibility and public image,• Reduce safety risk in product quality and safety,• Increases consumer confidence in your products,• Helps to decrease operating costs due to rework and penalties due to non-compliance,• Helps boost export opportunities,• Reduced duplication of inspections,• Cost saving.

What are the GMP requirements?
704(a) of the FD&C Act. Rigorous adherence to good manufacturing practice minimizes the risk of adulteration or misbranding of cosmetics Guidelines• Building and Facilities. • Equipment. • Personnel. • Raw Materials. • Production.• Laboratory Controls. • Records. • Labeling.
GMP sometimes is referred also being as “cGMP”. The “c” stands for “current,” asking manufacturers that they must employ current and advanced technologies and systems that are up-to-date to comply with the regulation. Systems, Infrastructure, and Equipment are being used to proactively prevent issues, problems, contamination, mix-ups, and non-contaminations and errors, which may have been very good some years ago, but during current/modern times, maybe less than adequate by current standards.

CDG provide GMP certification in India.

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WHO GMP Certification in India.

CDG provide Who GMP Certification services to our valued patrons. GMP is a term that refers to the Good Manufacturing Practice Regulations promulgated by the US Food and Drug Administration under the authority of the Federal Food, Drug, and Cosmetic Act.
Further, systems and equipment used to prevent contamination, mix-ups, and errors are adequate by today's standards.

Other details:

Recognized worldwide for the control and management of manufacturing and testing of food and pharmaceutical products

Takes quality assurance approach

Ensures that products are consistently produced and controlled to the quality standard appropriate to their intended use

Enabling companies to minimize or eliminate instances of contamination

Applications:

Pharmaceutical

Medical equipment

Food Industries

CDG provides tailored solutions to all kinds of GMP compliance issues. With extensive experience of the GMP certification process, our regulatory experts will provide all the support you need to achieve GMP excellence.

GMPs can also help for compliance purposes, as regulatory bodies such as the FDA require the implementation of GMPs. For instance, GMPs are part of the FDA’s Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Human Food Rule, an aspect of FSMA that became final in 2015 which applies to nearly all food companies.

There are many binding requirements of current GMPs (CGMPs), including:Qualification of employees who manufacture, process, pack, or hold food to perform their assigned dutiesEducation, training, and/or necessary experience for employees to ensure the food they manufacture, process, pack, or hold is clean and safe, including training in the principles of food hygiene and food safetyGMPs to address allergen cross-contactGMPs for holding and distributing human food by-products used for animal food.

The role of GMP in food industry success is critical—they help food and beverage companies maintain food safety and quality while increasing their productivity. All relevant food legislation, including the FDA’s Food Safety Modernization Act (FSMA), emphasizes these practices, including customer certification requirements. 

GMPs help manufacturers improve the production of their goods. When followed precisely, they promote consistency in procedures and products within a safe environment to reduce the risk of recalls, contamination, and profit loss.

While GMPs are primarily used in the food industry, they also apply in the production of:

Beverages

Cosmetic products

Pharmaceuticals

Dietary supplements

Medical devices

To fully understand the importance of GMPs, it’s helpful to look at why they were developed. Prior to their existence, several noteworthy safety incidents in the U.S. were caused by food and medicine issues. The history of GMPs dates back to 1906, with many key milestones that have led to the practices we know today.

CDG Certification Ltd. counted among the leading firms that are engaged in rendering services for ISO 9001 Certification Services.

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• Delivery Time: 7 days

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CDG provide GMP certification in Bangluru.We are the leading organization in India for GMP certification services.

What is GMP certification in food industry?Good Manufacturing Practices (GMP) certification from CDG ensures the integrity of your food manufacturing process as well as your compliance with food safety regulations. Assurance of the safety and quality of food is an important consideration for consumers today.Certificate in GMP in Manufacturing, Packing or Holding of Human Food Good manufacturing practices (GMP) are essential to any organization looking to reduce the risk and liability that can result from poor handling within a food operation. This programme come across common dangers associated with manufacturing. This programme helps in management of organization's processes and ensuring complete control over general hygiene procedures and environmental contaminants. This programme is beneficial for professionals from different streams who wants to start their stint in food sector or interested in updating their knowledge. Improved knowledge of GMP, Enhanced ability to identify potential food safety risks from GMP, Correct implementation of GMP and Compliance with global best practice are some of the benefits of programme.

Module
1 :Introduction to GMP and Food Industry Module
2 :Indian Food GMP Module
3 :GMP in manufacturing, packing or holding of human food Module
4 :Validation and Verification for Food Industry Module
5 :Conducting and facing first, second & third party auditsModule
6 :Complaint Handling and Product Recall (Food Industry)Module
7 :CAPA and Deviation management (Food Industry)Module
8 :Industry based case studies.

Easy ISO provides GMP certification consulting services to our valued customers. GMP is a term that refers to the rules of good manufacturing practice promulgated by the United States Food and Drug Administration under the authority of the Federal Food and Drug Administration.
In addition, the systems and equipment used to avoid contamination, confusion, and errors are adequate according to current standards.
GMPs are all-encompassing in manufacturing—CDG cover every aspect of each process to prevent risks that could develop anywhere in the supply chain or manufacturing environment. CDG's goal is to maintain the integrity of products with sound operating procedures, ensuring the highest standards are met through every step from testing and development to storage. By following GMPs, food industry professionals can expect to mitigate contamination, testing failures, problems caused by environmental factors, and potentially harmful deviations.\

Because consumers can’t always tell whether food products are safe just by looking at them, manufacturers have a tremendous responsibility to provide safe, quality goods to the public. Following GMPs helps to promote quality, ensuring safe products for mass distribution. This increases the likelihood of products being free of dangerous substances or contaminants that could cause harm to consumers.
CDG provides tailored solutions to all kinds of GMP compliance issues. With extensive experience of the GMP certification process, CDG's regulatory experts will provide all the support you need to achieve GMP excellence.

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• Delivery Time: 7 days

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Quality and Certificates for Ayurveda Products With the spread of Ayurveda in the West also countless Ayurvedic products have come onto the market: massage oils, teas, cosmetics, food supplements and herbal preparations. Since the question of the quality of products is absolutely justified, partly because the media already have been reported about several occasions over quality defects (eg heavy metal pollution).
As in all areas, there are also different views what makes an ayurvedic product of high quality. Important for you as a consumer is to scrutinize the products critically and to receive specific information. You can also consult an Ayurvedic practitioner. Ultimately, you decide which quality features are important to you and how much you want to pay for it.In Ayurveda there are preparations - called Bhasmas - that process in a complex, repeated processes basic substances of metals and minerals that should be harmless in the correct preparation for the human body. This preparations are not admitted in Europe! Effective and consistent quality controls do not exist to a sufficient extent in India yet.The simplest features of a qualitative good ayurvedic product are as follows:• Products made from natural ingredients, without chemical additives• Certification by a recognized quality label-CDG• Laboratory tests, which were carried out in India• Traditional Ayurvedic products are manufactured on the basis of herbs. Therefore massage oils with essential oils are not part of the traditional Ayurveda.

CDG is a leading organization of the industry, dedicatedly engaged in offering an optimum quality array of WHO GMP Certification Services for our esteemed customers. Good manufacturing practice (GMP) is the part of quality assurance which states that products are consistently produced and controlled to the quality standards during production appropriate to their intended use and as required by the marketing authorization.


Other Details:• Flexible approach• Use advanced technologies• Crystal clear dealings• Timely executed Being the first GMP certified Ayurvedic Medicine Manufacturing Plant in the world, ISO 9001:2015 and DSIR recognized research and development laboratory, we at CDG give utmost priority to the quality we achieve in each step - right from raw material sourcing to the end finished products.
Standardization and Certification of Ayurvedic Products
For Pharmacopoeial standardization of Ayurvedic drugs, two organizations, namely, Pharmacopoeia Commission for Indian Medicine and Homeopathy (PCIM&H) an autonomous body and Pharmacopoeial Laboratory for Indian Medicine (PLIM) have been established by the Government of India.
There are two Voluntary Certification Schemes for Ayurveda products.
1)      Certification scheme of Quality Council of India (QCI) an autonomous body and
2)      Certificate of Pharmaceutical Products (CoPP) for Ayurveda product issued by Drug Controller General of India (DCGI) for the purpose of export.
QCI Scheme provides two kinds of certificates:
a.       AYUSH Standards Mark for the Ayurveda products complying with domestic regulations. and;
b.      AYUSH Premium Mark for the Ayurveda products complying with International norms.

Our motive is to keep up with the advancements and regulate the processes to produce superior quality medicines.
CDG provide  GMP certification For Ayurvedic Product in  India.

Additional Information:

• Delivery Time: 7 days

Service Details:

A good manufacturing practice (GMP) is a production and testing practice that helps to ensure a quality product. Many countries have legislated that pharmaceutical and medical device companies must follow GMP procedures, and have created their own GMP guidelines that correspond with their legislation. Basic concepts of all of these guidelines remain more or less similar to the ultimate goals of safeguarding the health of the patient as well as producing good quality medicine, medical devices or active pharmaceutical products.



GMP Gap analysis audit: We will visit your site and perform an audit to determine where you need to improve your processes, documentation, and operations. We have experienced people able to perform GMP Audit Readiness/GMP GAP assessments for your facility against GMP requirements. We are also able to offer assistance in correcting any deficiencies found. MP compliance is viewed today as an essential baseline of food safety for food packers, processors manufacturers, and greenhouses.

Good Manufacturing Practices (GMP) certification from CDG certification ltd. ensures the integrity of your food manufacturing process as well as your compliance with food safety regulations. Assurance of the safety and quality of food is an important consideration for consumers today. A GMP is an important enhancement to your food safety management system, which increases your customers’ confidence in your commitment to trading and producing safe, high-quality food.

5 Key Components of Good Manufacturing Practices• Primary Materials and Products.• Premises.• People.• Procedures.• Processes.Qualified FDA GMP consultants can help your company plan, implement, and maintain systems to ensure GMP compliance. The good GMP consultants may recommend modern technologies and proven processes to achieve higher quality and more efficient processes.Through a free and objective demeanour, with our aptitude, we are more than proficient to help our worldwide clients. CDG's way of thinking is to give individual thoughtfulness regarding client sand to construct long-haul connections. We have an independent venture custom where our standing, respectability, quality, and administration is as critical to us as our business returns.

Good manufacturing practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.

The main risks are: unexpected contamination of products, causing damage to health or even death; incorrect labels on containers, which could mean that patients receive the wrong medicine; insufficient or too much active ingredient, resulting in ineffective treatment or adverse effects. GMP covers all aspects of production; from the starting materials, premises and equipment to the training and personal hygiene of staff. Detailed, written procedures are essential for each process that could affect the quality of the finished product. There must be systems to provide documented proof that correct procedures are consistently followed at each step in the manufacturing process - every time a product is made.

WHO has established detailed guidelines for good manufacturing practice. Many countries have formulated their own requirements for GMP based on WHO GMP.

Service Details:

CDG Provides GMP Certification Services in Pune.

CDG is a leading organization of the industry, dedicatedly engaged in offering an optimum quality array of WHO GMP Certification Services for our esteemed customers.
Good manufacturing practice (GMP) is the part of quality assurance which states that products are consistently produced and controlled to the quality standards during production appropriate to their intended use and as required by the marketing authorization.A Good Manufacturing Practices (GMP) certification scheme provides independent verification and certification that the basic manufacturing practices and prerequisites necessary for the implementation of an effective Hazard Analysis Critical Control Point (HACCP) food safety program are being followed.
Benefits of GMP Certification• Empower certification holders to opt great creation,• Timely identify of manufactures and the management issues,• Compliance with important laws and guidelines,• Improve overall credibility and public image,• Reduce safety risk in product quality and safety,• Increases consumer confidence in your products,• Helps to decrease operating costs due to rework and penalties due to non-compliance,• Helps boost export opportunities,• Reduced duplication of inspections,• Cost saving.

What are the GMP requirements?
704(a) of the FD&C Act. Rigorous adherence to good manufacturing practice minimizes the risk of adulteration or misbranding of cosmetics Guidelines• Building and Facilities. • Equipment. • Personnel. • Raw Materials. • Production.• Laboratory Controls. • Records. • Labeling.

What is the Procedure to get GMP Certification?
Application. This is the initial step to get the GMP certification; the application covers some essential data of the organization.• Review of Application. • Analysis & Agreement.• Documentation Review.• Granting Of Certification.• Surveillance Audit.

CDG is one of the platforms which coordinate to fulfil all your legal and financial requirements and connect you to consistent professionals. Yes, our clients are pleased with our legal service! Because of our focus on simplifying legal requirements, they have consistently regarded us highly and providing regular updates.GMP standard regulations address issues (internal/external) including documentation, procedures, SOPs, record keeping, personnel qualifications & awareness, sanitation, cleanliness, equipment verification, process validation, and complaint handling; packaging and labeling, etc. Most GMP standard guidelines and CFR requirements are very general, as normally standards are, accepting manufacturers themselves to decide respectively how effectively to interpret and implement the necessary controls. This means that it provides more tractability, but also generically requires that the manufacturer company effectively interpret the guidelines and requirements in an approach that will make sense for each business.
GMP sometimes is referred also being as “cGMP”. The “c” stands for “current,” asking manufacturers that they must employ current and advanced technologies and systems that are up-to-date to comply with the regulation. Systems, Infrastructure, and Equipment are being used to proactively prevent issues, problems, contamination, mix-ups, and non-contaminations and errors, which may have been very good some years ago, but during current/modern times, maybe less than adequate by current standards.Our clients can also track at all times the progress on our platform.

If you have any questions about the GMP Certification process, our experienced representatives are just a phone call away.
CDG provides the GMP Certification in India.

Additional Information:

• Delivery Time: 10 days

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CDG Provides GMP Certification Services in Hyderabad.

GMP Certification GMP refers for the goods manufacturing practices.GMP Certification is mainly developed for the natural and pharmaceutical product manufactures. It is a set of guidelines that gives you the assurance that your product is safe and correct. It is mainly dedicated for the food manufactures and medication manufactures and GMP provides assurance for produce safe and quality products according to the Quality standard. GMP is responsible for the safety, efficiency and quality of pharmaceutical products and medical devices.

WHO guidelines GMP certification?
WHO good manufacturing practices. Good manufacturing practice (GMP) is that part of a quality management system to ensure that products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the marketing authorization.

Benefits of GMP Certification• Improves brand value or image in the market• Provide guideline on how to produce safe and quality products.• Develops customer satisfaction by deliver the safe and quality product and services.• Develops motivation and team work between the employees of the organization.

What are GMP services?What is good manufacturing practice (GMP)? Good manufacturing practice (GMP) is a concept that ensures medical products are consistently produced and controlled according to quality standards. It is designed to minimize the risks to the patient involved in any pharmaceutical production.

Process to get the GMP Certification• Application:- This is the first step to get the GMP certification, the application covers some basic information of the company. The certification body must accept the application and needs to b record or maintain all the information on the GMP database.• Review of Application:- The application received shall be reviewed by the team to ensure that the compliance requirement have been fulfilled.• Quote and Agreement:- After the review of documents we provide the price quotation to the client and performs the Gap Analysis to cover all the clauses and section of the quality standards and Gap Analysis is done to check the Gap between company planned things and achieved things.• Documentation Review:- check the document of the organization to ensure that the documentation fulfilled the compliance requirement.
CDG's expertise is specialized in life sciences including:• The pharmaceutical industry• Medical devices• Biotechnology industries
Additionally, we offer testing and qualification services in the following industries:• Biorepository/blood banking• Cosmeceutical• Nutraceutical• Food and beverage• Hospitals

CDG is an autonomous specialized assistance organization and CDG has been giving examination benefits constantly for over 10 years. Our fundamental beliefs are well-being, quality, and honesty. We center around conveying a complete answer for any examination needs while incorporating our administrations with our clients' tasks and timetables. Through a free and objective demeanour, With our aptitude, we are more than proficient to help our worldwide clients. CDG's way of thinking is to give individual thoughtfulness regarding client sand to construct long-haul connections. We have an independent venture custom where our standing, respectability, quality, and administration is as critical to us as our business returns.

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• Delivery Time: 10 days

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CDG Provides GMP Certification Services in Chennai.GMP refers to the Good Manufacturing Practice Regulations.GMP certification is granted to manufacturing or service systems of organizations to certify that they engage with good manufacturing practices in their manufacturing or service processes, according to a Standard Code of Practice related to their business.
GMP regulations address issues including:
• Record Keeping• Equipment Verification• Personnel Qualifications• Process Validation• Sanitation• Complaint Handling• Cleanliness
Is GMP really that important? What’s all the fuss about? The short answer is yes. In fact, GMP is a globally recognized standard and quality assurance system. It is unquestionably reliable and effective as it covers all aspects of the production process.• GMP is a vital standard that all factories must adhere to in order to ensure the safe and consistent production of consumables that will not harm the general public• As it is globally recognized, consumers and foodies all over the world trust and respect itIn a nutshell, if you wish to succeed as a factory owner today, complying with GMP is an essentiality. For the safest, most hygienic, and efficient establishment; and the consistent production of superior quality products that meet international standards, GMP is indeed of paramount importance.
Good manufacturing practice is a fundamental requirement that when adhered to strictly and without deviation, can bring a wide variety of advantages for all.
Here are the ten main benefits of quality GMP:1. Your consumers ultimately receive products that are high quality, safe, and suitable for consumption2. GMP provides a clear production guideline ensuring that your products meet the expected standards of quality3. Reduce the number of errors or deviations that result in non-standard products (consistency is vital for maintaining your brand reputation)4. Creating a safe and convenient environment for your employees while working5. Encourage a positive attitude among your employees (it is paramount that they believe in and respect the value of GMP)6. Establishing a simple and standardized system for tracking data and information (GMP makes these processes easier, saving valuable time)7. Bolster management, supervision, and assessment flexibility8. Prevention of defects presenting themselves in the production process and eliminate any risk of repeat issues9. Improves the overall quality of food production across the board (and reduces production costs)10. Promotes a healthy control system enabling your facility to maintain the highest cleanliness and sanitation standards

Why choose CDG?CDG clients choose us in preference to others for a variety of reasons.
In most cases, it’s because they like our fair and practical approach throughout the entire certification process and how we understand and meet each individual client’s needs. In short: the quality of our service.
Benefits of working with CDG• Network of Overseas Strategic Partners• International Accepted Certificates• Recognized Worldwide• Industry Experienced Audit Team• Defined & Agreed Project Timescales• Fixed Cost & Competitive Quotations

Additional Information:

• Delivery Time: 7 days

Service Details:

CDG Provides GMP Certification Services in Ahmedabad.

Good manufacturing practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product. The main risks are: unexpected contamination of products, causing damage to health or even death; incorrect labels on containers, which could mean that patients receive the wrong medicine; insufficient or too much active ingredient, resulting in ineffective treatment or adverse effects. GMP covers all aspects of production; from the starting materials, premises and equipment to the training and personal hygiene of staff. Detailed, written procedures are essential for each process that could affect the quality of the finished product. There must be systems to provide documented proof that correct procedures are consistently followed at each step in the manufacturing process - every time a product is made. WHO has established detailed guidelines for good manufacturing practice. Many countries have formulated their own requirements for GMP based on WHO GMP. Others have harmonized their requirements, for example in the Association of South-East Asian Nations (ASEAN), in the European Union and through the Pharmaceutical Inspection Convention. We help you in compliance with WHO-GMP guidelines.

Benefits of GMP Certification
1. A Facility / Company / Organization can reap the following benefits, amongst others, from implementing and Certification towards GMP or cGMP: Establishes the fact that the Organization is following to Guidelines set by WHO or FDA and including Local Nationalized standards and Guidelines.
2. Ensures hygiene and cleanliness requirements throughout the Manufacturing and Logistics Chain.
3. Good Documentation Practices- documents (eg. Manual, Procedures, SOPs, operational Controls, Risk Assessment, Regulatory Compliances, etc) and Records for evidence.
4. Design and Operation including management of processes and products related to Medical Devices, IVD products / Items, Medicines/Drugs/pharmaceuticals, active pharmaceutical ingredients, Diagnostics products/items, and Food items.
5. Establishes the Competence (including Technical) of Personnel.
6. Establishes the Organization’s system of handling Non-Conformities and Complaints, including proper reporting to Regulatory bodies, wherever required.
7. Reduction of Costs and best possible Utilization of Resources.
8. Evidence of Safe and Quality Products and Items.
9. Compliance with all International and National and Local Regulations.
10. Builds Customer Assurance and Rapport and Trust.
11. Entry to International Markets.
12. Professional Culture within the organization.
13. Reduction of Complaints, Fines, Product Returns, Re-processing, Rejections, Non-Conformities, and Claims.

If you have any questions about the GMP Certification process, our experienced representatives are just a phone call away.

CDG will ensure that your communication with professionals is charming and seamless.

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• Delivery Time: 10 days

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CDG Provides GMP Certification Services in Sonipat.

What is Good Manufacturing Practice (GMP) Certification?Good Manufacturing Practice (GMP) is a system for ensuring the products are consistently produced and controlled according to the quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.
GMP forms an important part of the overall HACCP food safety system in a food business. Good manufacturing practices are important in order to produce safe food. The food business has a legal and moral responsibility to produce and prepare food that will not harm the consumer. There can be a high cost to the food business if it does not implement adequate Good manufacturing practices.
Certifying your food safety management system against Good Manufacturing Practices requirements is an excellent way to prepare for inspections by regulatory authorities and other stakeholders. The process will help you to demonstrate your knowledge of the importance of producing and trading safe, quality food.
Benefits of Good Manufacturing Practice (GMP) Certification • Customer SatisfactionMeet your customer expectations consistently.• Attract More CustomersBoost your brand reputation and stand out from the competition• Quality ImprovementMonitor, manage and improve the quality of your product with ease• Worldwide Recognition Attain worldwide reputation and access international trade.• Legal ComplianceMeet food safety legal compliance and corporate requirement• Improve ProcessesIdentify and eliminate waste within and between processes, reduce errors, and avoid rework.
Whom is Good Manufacturing Practice (GMP) Certification For?GMP is applicable to all organizations in the food chain that are directly or indirectly involved include, but are not limited to,
1. Food manufacturers
2. Retailers
3. Catering services
4. Cleaning and sanitation services, transportation, storage and distribution services
5. Suppliers of equipment
6. Cleaning and disinfectants
7. Packaging materials and other food contact materials
8. Feed producers, animal food producers, harvesters of wild plants and animals, farmers, producers of ingredients.
Take a Deep Dive Into GMP Certification Looking to implement Good Manufacturing Practice (GMP) system but not sure where to start? Take a look at our GMP guide here. The free guide will give you a great insight into this certification.
Steps to Good Manufacturing Practice (GMP) Certification
Step - 1 Application for GMP certification
Step - 2 Single-stage Certification audit
Step - 3 Issue of certificate on successful completion of certification audit
Step - 4 Surveillance audits at a defined period
Step - 5 Recertification audit after 3 years.

What is the Procedure to get GMP Certification?• Audit. Calculate your associations recorded approach and strategies against the consistence requirement.• Survey. Then, review the documentation of your administration structure to guarantee that the consistence prerequisites have been settled down.• Restorative activity. • Check.


CDG provides tailored solutions to all kinds of GMP compliance issues. With extensive experience of the GMP certification process, our regulatory experts will provide all the support you need to achieve GMP excellence.

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• Delivery Time: 7 days

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CDG Provides GMP Certification Services in Kanpur.India's Leading GMP Certification Provider.
We can help you to get your business GMP Certified.GMP stands for Good Manufacturing Practice, & the term is used globally for managing the control and management of manufacturing, testing and overall quality of pharmaceutical products. It defines certain guidelines that talks about the quality assurance approach. GMP certification ensures that products are produced following the quality standard norms.Compliance with GMP requirements entails minimum common sense sanitary and processing requirements applicable to all food processing establishments. Many food industry companies have implemented the GMP certification scheme for food processing as the foundation upon which they have developed and implemented other quality and food safety management systems, including HACCP, ISO 22000, SQF and ISO 9001.
Good Manufacturing Practices for Medical Devices The Key to Keeping a Product on the Market.GMP Regulations• Manufacturer:• Designs, manufactures, fabricates, assembles or processes a finished device• Includes: contract sterilization, installation, relabeling, remanufacturing, repacking, or specification development & initial distributors of foreign entities• Finished Device• Any device or accessory to any device• Suitable for use Capable of functioning• Whether or not packaged, labeled, or sterilized• Finished devices intended to be commercially• distributed for human use• Manufactured, imported or offered for import in the US• Establishes basic requirements for manufacturers of finished devices• Exemptions: Class I, IDE, component manufacturers.
Identification and TraceabilityIdentification: Procedures must be established and maintained for identifying product during all stages of receipt, production, distribution, and installation.
Traceability: Each device intended for surgical implant, to support or sustain life, or that can be result in significant injury to the user shall be identified with a control number, and identified in the device history record.
 Document Controls• Each manufacturer shall establish/ maintain procedures to control all documents• that are required by this part.• Document approval and distribution must be controlled.• Changes to documents must be approved and documented.• Records of all approvals and changes must be maintained.
Quality SystemRequirementsManagement responsibility:• Management Representative• Management Review• Quality Planning• Quality auditEstablish procedures and conduct quality audits to assure the quality system is in compliance with the QSR.• Personnel Ensure that personnel have training and experience for their responsibilities. 
Our clients can also track at all times the progress on our platform. If you have any questions about the GMP Certification process, our experienced representatives are just a phone call away.
CDG will ensure that your communication with professionals is charming and seamless.

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• Delivery Time: 7 days

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CDG Provides GMP Certification Services in Chandigarh.

Is GMP certification mandatory?GMP protects the product from any defect and maintains consistency in quality. People, processes, premises, products, and procedures including paperwork are 5PS on which GMP focuses. In certain regulated segments, a product can be considered “adulterated” if the product breach or does not obey current good manufacturing guidelines which although has passed all the specified tests. Therefore, GMP is mandatory in such areas. If QA/QC, Logistics are present then it is the organization’s call to implement GMP.

What is GMP certificate?
Good manufacturing practice (GMP) describes the minimum standard that a medicines manufacturer must meet in their production processes. The European Medicines Agency (EMA) coordinates inspections to verify compliance with these standards and plays a key role in harmonising GMP activities at European Union (EU) level.

Requirements of GMP Certification
1. Manufacturing facility design, Equipment and Machinery design, procedures & operating principles, and environmental conditions must be controlled.
2. Manufacturing practices and processes including health & safety, maintenance, etc must be clearly defined, validated, and controlled to ensure consistency and compliance with specifications.
3. Operators should be aware and trained and made competent to carry out the production, QA/QC, Logistics, Factory Management, and control of products for the full stages of production.
4. Records should be maintained for manufacture and quality control, and logistics- thereby demonstrating that all the necessary steps required by the defined procedures and instructions.
5. Records should be maintained for 5 to 10 years- based on regulatory requirements.
6. A system must be maintained and established for recalling any batch from
7. Sale or supply.

What are the 3 importance of GMP?
Good Manufacturing Practices help ensure the proper design, monitoring, and control of manufacturing processes and facilities, while securing the identity, strength, and quality of their products.

Other Details:• Flexible approach• Use advanced technologies• Crystal clear dealings• Timely executed
Manufacturer''s Advantages
One of the main advantages is that the manufacturer''s quality systems and quality compliance have greatly improved. These gains were visible in the months coming up to GMP certification and continued in the years following certification.
In the pharmaceutical sector, GMP is followed.GMP refers to a system of rules, rules, and procedures that govern the processing of drug substances and products, medical equipment, medical product categories in vivo and in vitro, and food items.
The term GMP refers to pharmaceutical product production supervision and management, as well as quality control monitoring.
In most cases, the certification is valid for three years.Everyone in the pharmaceutical sector should understand why GMP requirements are necessary, with the goal of preventing disasters.We provide WHO GMP certification in following areas of India.

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• Delivery Time: 7 days