GMP Certification

What is GMP Certification?

GMP stands for Good Manufacturing Practices and is a set of guidelines developed for manufacturers of natural and pharmaceutical products. It ensures that the products are safe and manufactured correctly. GMP is primarily dedicated to food and medication manufacturers and provides assurance that they produce safe and high-quality products in compliance with quality standards. GMP is responsible for ensuring the safety, effectiveness, and quality of pharmaceutical products and medical devices.

Rietway Consultants GMP Package

The Services which are included in our package are as Follows:
✅ Consultation for GMP
✅ Preparation of Documents
✅Application Filing
✅GMP Certificate

Documents Required for GMP

1. Business Registration Proof
2. KYC of Proprietor/Partners/Directors
3. Objectives of Business
4. Email Id and Phone Number
5. Current Electricity Bill

GMP Procedure

Step -1 Arrange all Required Documents: The first step is to arrange all the documents and send the same over the email / WhatsApp to us. Once all the Documents are Received, we will Start the Further Process.
Step – 2: Preparation of Documents: The Next Step is Preparation of Documents to be Submitted at Department.
Step – 3 : Filling Of Application For GMP : The next Step is Filling Of Application for GMP.
Step – 4: After approval of the application Department Issues GMP Certificate.

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.

Is GMP Necessary If There Is A Quality Control Laboratory?

Ensuring good quality during the manufacturing process is important because it is not always feasible to test the final product. GMP helps to prevent errors in the manufacturing process that could lead to quality issues in the final product. Without GMP, it is difficult to ensure that each unit of a medication is of the same quality as those tested in the research facility. By adhering to GMP guidelines, companies can ensure the consistent quality of their products and reduce the risk of errors that may impact product safety and efficacy.

FAQ on GMP Certification

Who Issues GMP Certificate?
A manufacturer is eligible for a GMP certification after undergoing a thorough GMP assessment to ensure compliance with GMP guidelines. The certification is only granted if the necessary documentation related to the assessment is found to be satisfactory. The GMP certification indicates that the manufacturer is in compliance with GMP guidelines and includes information such as the date of the most recent assessment and the specific activities and regulations that were reviewed.

What is GMP inspection?
Pharmaceutical manufacturing facilities are inspected to ensure compliance with Good Manufacturing Practice (GMP) standards, as well as to grant authorization for the production of specific pharmaceutical products that are usually associated with an application for marketing approval.

Why is GMP important?
Pharmaceutical manufacturing facilities are inspected either to ensure compliance with Good Manufacturing Practice (GMP) or to grant approval for the production of specific pharmaceutical products, typically in connection with an application for marketing approval.

What is the Validity of GMP certification?
Each certificate is valid for a period of 3 years from the date of issue.