Current Good Manufacturing Practices

Good Documentation Practices

Data Integrity

Cleanroom Behaviours

Contamination control

GMP Behaviour

• Investigation and Root cause analysis

• Investigation of human error

• Change control management

• Corrective action and Preventive action

• Investigation of OOS results

• Audit etiquettes

• Self Inspection and All-Time Audit Readiness

• Handling regulatory inspections

• Pharmaceutical Quality Management System

• IT Compliance

• Stability studies

• Quality Risk Management

• Good Chromatography Practices

• Good Quality Control Practices

• Handling of OOS results

• GMP Trainer certification

• Transport Validation

• Qualification of clean rooms

• Process validation

• Cleaning validation

• Equipment and area qualification

• Analytical Method Validation

• Computer system validation

• Principles of Sterilization

• Pharmaceutical Water

• Technical Basics of formulation equipment

• Technical Basics of formulation process

• Technical basics of analytical instruments

• Technical fundamentals of chemical analysis

We support organizations to establish and implement employee training policy, training procedure, training effectiveness, learning management system and integrated capability building approach.

We provide product training solutions for medical sales representatives and pharma field sales staff