WHO-GMP Audit In Mumbai

Good manufacturing practice applicable for all healthcare manufactures such as active pharmaceutical ingredients, diagnostics, foods, pharmaceutical products, and medical devices. GMPs are guidelines that outline the aspects of production and testing that can impact the quality of a product. Many countries have legislated that pharmaceutical and medical device companies must follow GMP practicesas per GMP guidelines that correspond with their legislation The South African Regulatory Authority describes GMP as "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 medicine registration or product specification. GMP is concerned with both production and quality control.

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.

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

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.