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.
The Services which are included in our package are as Follows:
✅ Consultation for GMP
✅ Preparation of Documents
✅Application Filing
✅GMP Certificate
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.
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?
Good quality can be assured during the manufacturing process afterwards it is not possible to
test it. GMP protects the final product from errors that cannot be ignored through quality
product. Without GMP it is difficult to be certain that each unit of a medication is of a similar
quality as the units of medication tested in the research facility.
Who Issues GMP Certificate?
A GMP certification is given based on a finished GMP assessment of a producer working as
per the GMP guidelines. The authentication is given that satisfactory documentation on the
examination follow-up is submitted.
The GMP certification pronounces that the maker agrees to GMP, and the certificate
incorporates a reference to the latest date of the genuine review, just as which exercises and
under which enactment they have been investigated.
What is GMP inspection?
The purpose of inspecting pharmaceutical manufacturing offices is either to implement Good
Manufacturing Practice (GMP) consistence or to give approval to the manufacturing of
explicit pharmaceutical items, generally corresponding to an application for marketing
approval.
Why is GMP important?
The purpose of inspecting pharmaceutical manufacturing offices is either to implement Good
Manufacturing Practice (GMP) consistence or to give approval to the manufacturing of
explicit pharmaceutical items, generally corresponding to 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.