• Provide Qualified persons duties as per EU requirements (article 51 of EC Directive 2001/83/EC and Article 55 of EC Directive 2001/82/EEC.
  • Experienced QP’s in disposition  of different final dosage forms –including Tablets, Capsules ,Liquids ,Steriles  and Biopharmaceuticals.
  • QP’s available for Batch Certification ( manufactured within and outside EU )  and Investigational Medicinal Product .
  • Short or long term contracts.