• Project management and realisation for all stages (development to implementation of GACP-/EU-GMP-/GDP-concept),
• Development of High Level Documents (Site Master File, Validation Master Plan, Business Plan) and the necessary basic documentation (technical/process/quality management),
• Longterm cooperation with supplier and companies from the pharmaceutical industry,
• Partnership with SIEMENS, own tool „CVal“ for creating a digital twin (for optimization and simplifying the set up and datamanagement),
• Selection and establishing of analysis methods