Regulatory Affairs in Pharmaceutical Industry
In an industry governed by strict global standards, Regulatory Affairs serves as the bridge between pharmaceutical innovation and market access. This comprehensive course provides a…
Tag: Paid Manufacturing Course
Revised Schedule M: Self Inspection & Quality Audits
With the updated Revised Schedule M, the importance of self-inspection and internal quality audits has been significantly elevated to ensure continuous compliance and improvement. This…
Revised Schedule M: Manufacture of Oral Solid Dosage Forms (OSD)
The Revised Schedule M has introduced critical updates that impact the manufacture of Oral Solid Dosage Forms (OSD) such as tablets, capsules, and granules. This…
The Future of Smart Labs & Pharma World QUIZCON
Step into the future of pharmaceutical innovation with this unique QUIZ + CONFERENCE (QUIZCON) format event that blends knowledge, competition, and futuristic learning. “The Future…
Revised Schedule M: Premises & Equipment
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…
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…
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.…
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