Revised Schedule M: Complaints & Product Recall
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…
Tag: Paid Regulatory Course
Revised Schedule M: Materials, Vendor Qualification and Reference Standards
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.…
Revised Schedule M: Manufacture Of Oral Liquids
The Revised Schedule M has brought critical updates to the Good Manufacturing Practices (GMP) governing the manufacture of oral liquid pharmaceuticals, including syrups, suspensions, and…
Revised Schedule M: Manufacture Of Active Pharmaceuticals Ingredients
Stay ahead in regulatory compliance with an in-depth understanding of the Revised Schedule M—India’s updated framework governing the manufacture of Active Pharmaceutical Ingredients (APIs). This…
Revised Schedule M: Validation of Sterilisers & Aseptic Process
With the implementation of the Revised Schedule M, regulatory expectations for sterile pharmaceutical manufacturing have become more stringent—especially around validation of sterilisers and aseptic processing.…
Process Analytical Technology
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…
Preparing for an Unannounced Audit – What Regulators Look for in Analytical Labs
Unannounced audits can be a major challenge for analytical laboratories. This course equips participants with the essential knowledge and strategies to stay audit-ready at all…
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