Quality Risk Management
Quality Risk Management (QRM) is a core component of modern pharmaceutical quality systems, as emphasized by ICH Q9, Revised Schedule M, and global GMP regulations.…
Quality Risk Management (QRM) is a core component of modern pharmaceutical quality systems, as emphasized by ICH Q9, Revised Schedule M, and global GMP regulations.…
The Revised Schedule M has introduced stricter and more structured expectations around Qualification and Validation in pharmaceutical manufacturing. This course is tailored to help professionals…
With the Revised Schedule M, HVAC systems have gained renewed focus as a critical component in ensuring controlled environments, product quality, and regulatory compliance in…
Under the Revised Schedule M, Good Documentation Practices (GDP) have become even more critical to ensure data integrity, regulatory compliance, and traceability across all pharmaceutical…
The Revised Schedule M introduces stricter and more detailed requirements for pharmaceutical premises and equipment—aimed at enhancing product quality, minimizing contamination risk, and ensuring regulatory…
The Revised Schedule M places increased emphasis on robust systems for managing market complaints and executing product recalls effectively and compliantly. This course is designed…
With the rollout of the Revised Schedule M, the expectations around materials management, vendor qualification, and reference standards in pharmaceutical manufacturing have been significantly upgraded.…
Welcome to Pharmastate Academy’s comprehensive course on Process Analytical Technology (PAT) in Pharmaceutical Manufacturing. Discover how PAT transforms pharmaceutical manufacturing by fostering innovation and ensuring…
Pharma Professionals who are keen to understand Quality Systems in Pharma should take this course. You will find questions on Water for Pharmaceuticals, Sterilization, Quality…
In this course you will learn the Journey of Indian Pharmaceutical Industry from per-independence era to the current situation. In Chapter 1 you will see…