by Dr. Yashashwini Reddy | Sep 13, 2025
1. Equipment Design & Installation Equipment designed with GMP-compliant sanitary design (easy to clean, non-reactive materials). Materials of construction suitable (e.g., SS 316L for product contact). Installation Qualification (IQ) completed and documented....
by Dr. Yashashwini Reddy | Sep 13, 2025
GMP Audit Checklist – Weighing & Dispensing 1. Area & Environment Weighing/dispensing area dedicated, controlled, and clearly labeled. Differential pressure maintained between adjacent areas. Environmental conditions (temperature, humidity, cleanliness)...
by Dr. Yashashwini Reddy | Sep 13, 2025
1. System Design & Validation Water system (Purified Water, WFI, Potable Water) designed to meet pharmacopeial requirements (USP/EP/IP/JP). System qualification performed (DQ, IQ, OQ, PQ) with proper documentation. Risk assessment performed for potential...
by Dr. Yashashwini Reddy | Sep 13, 2025
GMP Audit Checklist – Personnel & Premises 1. Personnel 1.1 Organization & Staffing Adequate number of trained and qualified staff available. Organizational chart available and updated. Clear roles, responsibilities, and reporting lines defined. 1.2 Training...
by Dr. Yashashwini Reddy | Sep 13, 2025
Vendor Audit Checklist 1. General Information Vendor profile and organization structure available. Valid licenses, registrations, and certifications (GMP, ISO, GDP). Regulatory inspection history (FDA, EMA, WHO, local authorities). Change notification procedure in...
