A way forward has been found to resolve the differences between the EU's controversial guideline on good manufacturing practices for advanced therapies and the international guideline of the Pharmaceutical Inspection Co-operation Scheme (PIC/S) on the same topic.
PIC/S Finds A Way To Solve Divergences With EU ATMP Guide
A targeted stakeholder consultation will soon be launched on proposals to split the Pharmaceutical Inspection Co-operation Scheme's existing guide on biological products into two parts so as to focus separately on manufacturing issues specific to gene therapy and tissue-engineered products.
