Complete the process of GMP certification.
Provide all the required documents.
Our export will file your license & obtain the license.
GMP stands for Good Manufacturing Practice, and it is a word that is used around the world to describe the control and management of pharmaceutical product manufacturing, testing, and overall quality. It establishes a set of guidelines for the quality assurance methodology. GMP accreditation ensures that items are manufactured in accordance with industry standards.
(1) Empower certification holders to choose great creation.
(2) Timely identification of manufacturers and management issues.
(3) Adherence to key laws and guidelines.
(4) Improve overall trustworthiness and public perception.
(5) Reduce product quality and safety risks.
(6) Consumers will have more faith in your items as a result of this.
(7) Reduces operating expenses by reducing rework and fines for non-compliance.
(8) Increases export opportunities.
(9) Reduces inspection duplication.
(10)Saves money.
(1) Fill in the application form.
(2) Application Evalution.
(3) Analysis and consensus.
(4) Surveillance audit.
(5) Get your certificate.
(6) Examining the documents.
(1) Name of the applicant, including contact information.
(2) Making copies of licenses.
(3) Items that have been approved are listed.
(4) Information regarding the final formulation.
(5) The tools and instruments that will be utilized.
(6) A manufacturing plants layout.
(7) A water system showing a circulation loop and MOC.
(8) Proof of effectiveness and safety as per the rule 158B of the 1945 drugs and cosmetic rules.
(1) What is GMP Certification?
(2) What is the objective of GMP?
(3) What is GMP inspection?
(4) Why is GMP important?
(5) What are GMP guidelines?
