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.
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