Life science training courses and technological professional development

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. 

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 

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. 

You can work with us in two ways: 

Open courses 
Participate in scheduled life science training courses together with professionals and companies from the industry. 

Company-specific training programmes 
Tailored competence development programmes based on your own processes, technologies and quality requirements. 

The programmes can be based on your: 

• processes and workflows 
• quality and documentation systems 
• technical installations and production equipment 
• regulatory requirements and standards, such as MDR/IVDR 
• validation, calibration and audit activities 

The training can be combined with practical exercises, laboratory activities and workshops.