GMP
GMP Certification
GMP refers to the goods manufacturing practices. GMP Certification is mainly developed for natural and pharmaceutical product manufacturers. It is a set of guidelines that assures you that your product is safe and correct. It is mainly dedicated to food manufacturers and medication manufacturers and GMP ensures safe and quality products according to the Quality standard. GMP is responsible for the safety, efficiency, and quality of pharmaceutical products and medical devices.
Benefits of GMP Certification
- A period Improves brand value or image in the market
- Provide guidelines on how to produce safe and quality products.
- Develops customer satisfaction by delivering safe and quality products and services.
- Develops motivation and teamwork between the employees of the organization.
The process to get the GMP Certification
- Application:- This is the first step to getting the GMP certification, the application covers some basic information about the company. The certification body must accept the application and needs to 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 requirements have been fulfilled.
- Quote and Agreement:- After the review of documents we provide the price quotation to the client and perform the Gap Analysis to cover all the clauses and sections of the quality standards Gap Analysis is done to check the Gap between the company’s planned things and achieved things.
- Documentation Review:- check the document of the organization to ensure that the documentation fulfills the compliance requirement.
- Stage-1 Audit:- Evaluate your organization’s documented procedure and policies against the compliance requirement.
- Review:- Review the documentation of your management system to ensure that the compliance requirements have been met.
- Corrective action:- Corrective action is dealing with nonconformity. It is taken when nonconformity occurs.
- Verification:- Verify the documentation of the organization as per the standard requirements.
- Stage-2 Audit:- In stage-2 audit, the auditor verifies that the organization implements according to its documentation and if the auditor of the certification body identifies the non-conformities then the auditor allows correcting the non-conformities.
- Review:- Review the implementation process according to the organization’s document.
- Corrective Action:- If there is any nonconformity that occurs then the corrective action has been taken.
- Verification:- Verify work instruction and implementation process are being followed by your employees.
- Granting of Certification:- The Certification Body will issue a certificate of compliance, which is valid for three years.
- Surveillance Audit: A surveillance audit is conducted to ensure that the organization meets the requirements of the management system. A surveillance audit must be performed every six months or one year from the date of the issued certificate.
- Re-Certification:- Re-certification is the process, which is done at the end of a year.
- Review:- Review the documentation and implementation process of your management system to ensure that the compliance requirements have been met.
- Corrective Action:- Recheck the nonconformity, if any other problem occurs then CB allows the organization to resolve the non-conformity.
- Verification:- Compare the documentation of the organization with the compliance requirement.
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