Training modules/ workshops (Past, Current, and future)

In QUALITY AFFAIRS

  • Quality Risk Management
  • Validation: Process, Cleaning, Analytical, Equipment
  • CAPA and Failure Investigations
  • Microbiology in Pharma Manufacturing
  • GMP for Laboratories
  • Data Integrity and Audit Trails

In REGULATORY AFFAIRS

  • Regulatory Submissions for APIs and Drug Products
  • Audit Readiness : Preparing for and Facing Audits
  • MRP, DCP, e-CTD
  • Recent Warning Letters and Interpretations

In R&D / FORMULATION AND ANALYTICAL DEVELOPMENT

  • Stability Studies for Pharmaceuticals
  • Quality by Design and Design of Experiments
  • Analytical Method Development and Validation
  • Statistical Understanding and Use
  • Nasal and Pulmonary Drug Delivery Systems

In MANUFACTURING / TECHNICAL OPERATIONS

  • Isolators : Current Issues and Technologies
  • Cleanrooms : The Art of Compliance
  • Pharma Water and HVAC Systems
  • cGMP Systems : Technology and Practice

In CLINICAL RESEARCH

  • Medical Writing for Clinical Research Professionals