»Welcome! Since May 2011 Schaeffler-PharmaConsulting has been providing executive Research and Development Services for the Pharmaceutical and Biotech Industry to support your R&D projects from the pre-clinical stage through clinical phase I to IV to the approval of your Drug in key markets. With the long-lasting and broad experience in Quality, Regulatory Affairs and Clinical development of molecules, we develop the best strategy for your Rx project. Our expertise covers the development of New Chemical Entities, Biologics and Life-cycle projects and the majority of dosage forms. «

Quality

  • Drug Substance & Drug Product
  • Biologics & New Chemical Entities
  • Life-cycle projects
  • Quality Management

Regulatory Affairs

  • Scientific Advices
  • IMPDs & INDs
  • Technical summaries/expert reports
  • EU Centralized/DCP/MRP & NDA support

Clinical Development support

  • IMP Manufacture
  • Packaging design

Due Diligence

  • Cross-functional review
  • Implementation
  • Infrastructure
  • Strategy