by Dr. Yashashwini Reddy | Aug 18, 2025
Quality Inspection in Pharmaceuticals Quality inspection in pharmaceuticals is a critical step to ensure that drug products meet regulatory standards, patient safety requirements, and therapeutic efficacy. It involves systematic checks, tests, and verification across...
by Dr. Yashashwini Reddy | Aug 18, 2025
✅ 30 Common Ways to Avoid the Most Frequent GMP Errors Follow approved SOPs strictly. Ensure proper documentation – never backdate or predate entries. Maintain good record-keeping practices (ALCOA+ principles). Always perform line clearance before starting new...
by Dr. Yashashwini Reddy | Aug 18, 2025
Types of Purified Water Systems in Pharmaceuticals Pharmaceutical industries require high-quality water for manufacturing, cleaning, and formulation. Different water systems are designed to meet specific pharmacopeial standards (USP, EP, IP, JP) depending on their...
by Dr. Yashashwini Reddy | Aug 18, 2025
Top 5 Tips for a Successful FDA Inspection: ✅ Top 5 Tips Be Inspection-Ready Always – Maintain compliance at all times, not just when expecting an inspection. Ensure documentation, training records, SOPs, and facilities are always up-to-date. Ensure Documentation...
by Dr. Yashashwini Reddy | Aug 18, 2025
📌 Temperature and Humidity Validation/Mapping in Storage Area Overview:Temperature and humidity mapping is a critical activity in pharmaceutical warehouses, cold rooms, and storage areas to ensure that medicinal products are stored under controlled conditions as per...
