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QP release

Your QP for safe pharmaceutical products

All GMP activities are done under the supervision of EU qualified persons (QPs) located at our two GMP facilities. Our six full-time qualified persons are well-experienced in releasing various types of finished products (oral, topical, sterile and biological drugs as well as vaccines and blood products) according to European GMP standards.

Whether you need QP services for investigational, compassionate use/expanded access or commercial products, we can meet your requirements. 
 

 
Two printed documents are placed on a table for regulatory review

Ensuring quality and compliance: Auditing manufacturing and testing sites for qualification

For importing medicinal products into Europe, we also offer the qualification of third-country manufacturing and testing sites through audits, and the issuance of the QP declaration and application for  import permits. Our professional QPs are experienced and knowledgeable in global supply chain evaluations.

 
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