Pharmaceutical Training Services

Good Manufacturing Practices (GMP / cGMP)

Principles of GMP & cGMP
Facility & equipment hygiene
Documentation practices (BMR, SOP, Logbooks)
Data integrity & ALCOA+ compliance

Quality Management & Compliance

Quality Risk Management (ICH Q9)
CAPA (Corrective & Preventive Actions)
Deviation & change control handling
Internal & external audit readiness

Laboratory & QC/QA Training

GLP (Good Laboratory Practices)
Analytical method validation & calibration
Stability studies & documentation
Handling out-of-specification (OOS) & out-of-trend (OOT) results

Production & Operations Training

Equipment qualification & validation
Process validation (ICH Q8/Q10 principles)
Batch manufacturing process training
Cleaning & cross-contamination prevention

Regulatory & Documentation Training

Regulatory submission requirements (USFDA, EMA, CDSCO)
Technical dossiers & DMF preparation
Audit inspection handling (mock audits, FDA/WHO audit preparedness)
Serialization & traceability compliance

Specialized Training

EHS (Environment, Health & Safety) compliance
Pharmacovigilance & adverse drug reporting
Supply chain & GDP (Good Distribution Practices)
Soft skills for pharma professionals (leadership, communication, teamwork)