To simplify and expedite the QP release process
Almac has added a Qualified Person (QP) Facilitation Programme to its suite of QP services.
Offered to global clients importing investigational medicinal products (IMP) into the European Union for clinical trial, Almac has developed the programme to alleviate the logistical challenges surrounding the QP Release process, as well as to provide a deeper level of consultancy during this critical stage of clinical trial distribution.
The QP Facilitation Programme broadens Almac’s QP services portfolio, which currently includes regulatory guidance, global auditing and import testing.
Features of the programme include access to a dedicated Quality Compliance Manager on-site who will provide supply chain assessment, assembly and completion of relevant documentation necessary for QP Release, and an overall better understanding of the QP release process.