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Techno Service Academy provides professional training programs designed for Pharmacists, Chemists, Scientists, engineers, laboratory specialists, quality professionals, production technicians, R&D staff, and regulatory personnel across multiple industries.

Training Categories

audit

  • How to deal with Audits
  • Preparation of SFDA & EMA audits

laboratory management

  • Laboratory Management system
  • Good Laboratory Practices and Data integrity (GLP)
  • Laboratory Documentation and Lab Data integrity
  • Laboratory Safety
  • Laboratory Information Management System (LIMS)

qms asq 1

  • Risk Management
  • Good Documentation Practice and Documentation System Control
  • Data Integrity and Governance

pharmaceutical quality management system

  • Change Control
  • Deviation Handling and Root Cause Analysis
  • CAPA Management
  • Recall and Complaint
  • Self-Inspection
  • Product Quality Review
  • Management Review

iso management systems

  • ISO 9001
  • ISO 14001
  • ISO 13485
  • ISO 22000
  • ISO 45001
  • ISO 17025
  • ISO 22301:2012 Internal Auditor Training
  • Lead Auditor Training

good manufacturing practices

  • Advanced cGMP
  • cGMP Auditing
  • Good Manufacturing Practice (GMP) for Workers and Technicians
  • Induction Good Manufacturing Practice (GMP) for New Pharmacists and Chemists
  • Principles on Sanitation & Hygiene Practices in GMP for technicians and workers
  • In-Process Control (Roles, How, and Why)

validation

  • Computer System Validation
  • Process Validation and Bulk Hold Time Studies
  • Cleaning Validation and Hold Time Studies
  • Equipment & Water System Qualification
  • Calibration Management
  • HVAC and Premises Qualification
  • Thermal Mapping Studies
  • Statistical Process Control and Control Charts
  • Good Weighing Practice and Balance Qualification
  • Validation for Workers and Technicians

laboratory and analysis

  • HPLC basic principles and advanced course .
  • Analytical Method validation
  • HPLC trouble shooting advanced
  • HPLC Method development
  • Gas Chromatography (GC) basic principles
  • Excel Spreadsheet Design and Validation
  • Microbiology in Pharma Industry
  • Pharmaceutical Stability Management

r&d

  • Fundamentals of formulation  and manufacturing of Pharmaceutical Dosage Forms.
  • Quality By Design (QBD) and Design of Experiment

Who Should Attend?

• Laboratory Analysts

• Quality Assurance team

• Quality Control Specialists

• Production staff and technicians

• Validation team

• Maintenance Engineers

• Calibration team

• Regulatory Affairs Specialists

• HSE Professionals

• Supervisors

• Students & Fresh Graduates

Training Formats

Classroom Training

Recorded Online Training

On-Site Training

Live Online Instructor-Led Training

Customized Corporate Training