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Strengthen quality, compliance, and operational reliability in regulated environments

At Force Technology, we provide training courses and competence development programmes at the Academy for companies within pharma, medical device, biotech and laboratory environments. 

The courses support the development and maintenance of technical competences related to GMP, MDR, IVDR, quality assurance, documentation, validation, testing and operations in regulated environments. 

The training at the Academy is based on the technologies, processes and regulatory requirements that characterise the life science industry – from laboratories and production facilities to utility systems, technical installations and controlled environments. 

Turn GMP, quality and regulatory requirements into practice

The Courses at the Academy help you: 

  • strengthen competences within GMP, MDR/IVDR, QA/QC and regulatory compliance 
  • work systematically with documentation, validation and audits 
  • support stable processes and operational reliability 
  • develop technical competences within testing, measurement and inspection 
  • translate standards and regulatory requirements into practical implementation 
  • build a shared technical understanding across production, quality and engineering functions 

Technical competence development for pharma, medical device and biotech industries

The courses are relevant for companies and professionals working within: 

  • pharma and GMP-regulated production 
  • medical device industries and MDR-regulated products 
  • biotech and laboratory environments 
  • QA/QC and quality functions 
  • validation and compliance 
  • technical operations and maintenance 

 

The content is based on experience from industrial environments where traceability, quality assurance and documentation are essential – from development and production to testing, calibration and technical quality assurance. 

Find training courses within key technical areas

Courses

Quality and compliance

Gain insight into quality processes, audits, GMP, documentation and regulatory requirements within the life science industry.