A Review on Quality Agreement requirement in Pharmaceuticals by Regulatory Authority in Compliance to cGMP Guidelines

  • Suleman S. Khoja Resource person in Pharmaceutical Quality Assurance and Facility Audit
  • Sohil S Khoja Resource person in Pharmaceutical Quality Assurance and Facility Audit,
  • Farhad S Khoja Registered Pharmacist
  • Shamim S Khoja Registered Pharmacist
  • Narmin A. Pirani Registered Pharmacist
Keywords: Regulatory Authority, Compliance, cGMP Guidelines, Quality Agreement

Abstract

A quality agreement is a comprehensive written agreement between parties involved in the contract manufacturing of drugs that defines and establishes each party’s manufacturing activities in terms of how each will comply with CGMP. Quality agreements may be reviewed during inspections. A quality agreement describes the owner’s and the contract facility’s roles and manufacturing activities under CGMP.

Author Biographies

Suleman S. Khoja, Resource person in Pharmaceutical Quality Assurance and Facility Audit

Resource person in Pharmaceutical Quality Assurance and Facility Audit,
Vapi, Gujarat, India

Sohil S Khoja, Resource person in Pharmaceutical Quality Assurance and Facility Audit,

Resource person in Pharmaceutical Quality Assurance and Facility Audit,
Vapi, Gujarat, India.

Farhad S Khoja, Registered Pharmacist

Registered Pharmacist,
Gujarat State Pharmacy Council, Gujarat, India

Shamim S Khoja, Registered Pharmacist

Registered Pharmacist,
Gujarat State Pharmacy Council, Gujarat, India

Narmin A. Pirani, Registered Pharmacist

Registered Pharmacist,
Gujarat State Pharmacy Council, Gujarat, India

Published
2017-05-01
How to Cite
[1]
Khoja, S.S., Khoja, S., Khoja, F.S., Khoja, S.S. and Pirani, N.A. 2017. A Review on Quality Agreement requirement in Pharmaceuticals by Regulatory Authority in Compliance to cGMP Guidelines. PharmaTutor. 5, 5 (May 2017), 24-28.
Section
Articles