More than 33 years of expertise on international markets with specialisation in the pharmaceutical industry
Designated focus on:
- GMP (Good Manufacturing Practices) in the pharmaceutical production
- Supply-Chain-Management
- Consulting
More than 25 years of expertise in:
- Application, advancement and development of pharmaceutical extraction processes (i.e. enzymatic digestion, hydrolysis)
- Application, advancement and development of pharmaceutical filtration and synthesis processes (i.e. ultrafiltration, ion exchange)
- Pharmacopoeia conforming analyses
- Planning, setup and operation of pharmaceutical API (active pharmaceutical ingredients) and pharmaceutical intermediate factories (greenfield and existing)
- Development and advancement of quality management systems
- Downstream and upstream GMP-audits of pharmaceutical active ingredients and intermediate factories
- Audits of slaughterhouses and gutrooms as part of the API supply-chain
