Good manufacturing practice (GMP)


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GMP Certification.

roduct quality assurance is a major concern for companies involved in the pharmaceutical industry. Pharmaceutical companies must ensure the highest quality, safety and hygiene of the products produced on their premises. The products offered by pharmaceutical companies have a direct impact on the health and safety of consumers, so regulatory authorities must strictly control the quality of these products by putting in place appropriate quality standards.

GMP certification is one of the standards used by the pharmaceutical industry to ensure that the products offered have the highest levels of safety and hygiene and are perfectly healthy for consumers. Every company that manufactures pharmaceutical products must obtain a GMP certificate. Additionally, this standard applies to companies involved in certain processed foods. The guidelines contained in the standard cover all major aspects related to the manufacturing of medical products, including quality inspection of materials, manufacturing processes and finished products, and employee training.

Documents Required for ISO Certification

Registration Proof of Legal Entity

Bills of Purchase & Invoice Bill

Address Proof of The Company

Application
Form

PROCEDURE FOR ISO REGISTRATION

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Arrange Documents

You Are Required To Email The Required Documents (List Is Given Above).

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Consult Our Advisors

Consult Our Business Advisor Regarding Various Accreditation Body And Standards.

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Verification

Our Professional Will Verify The Validity Of Documents & Information Provided.

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Fees Payment

On Confirmation, Make Online Payment With Different Payments Modes Available

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Filing The Application

Carry ISO Consultancy, Documentation And Implementation.

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Certificate

On Successful Audit, Independent Certification Body Shall Issue ISO Certificate.