BII Global

Upcoming Training Programs

RCA CAPA & Deviation management

lifecycle Commissioning & Qualification

Extractable & Leachable

Biotech manufacturing processes

Advanced Therapy Medicinal Products (ATMPs) drug products in manufacturing

HVAC, and contamination controls

Pharmacovigilance & Inspection Audit

Effective R&D Project Management in Pharma & Biotech

Nitrosamines Impurities

AI – Analytical Method Validation

Chemistry, Manufacturing, and Controls (CMC) aspects of biopharmaceutical development.

OSD: Operations, Quality, Equipment and Technology

Pharmacokinetic-Pharmacodynamic Modeling

Bioavailability (BA) and Bioequivalence (BE)

Scale up, Validation & Tech Transfer (QBD)

Cleaning Validation

Impurities Profiling

GMP Compliance

Biopharmaceutical manufacturing facility design

PAT QbD

Analytical Instrument Qualification

Audit Trail Review for Computerized Systems in Analytical Laboratories

Aseptic Process & Annex 1

Freeze drying Technology

Stability Testing

CMC Regulatory Compliance

Quality Requirement for Biologics

CSV & Data Integrity in Pharma & Biotech

Lyophilization

Cross Contamination Control

Pricing & Reimbursement

Pharma 4.0

ICH Q8

Research & Innovations in Pharma

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