The European Commission is holding a second targeted stakeholder consultation on the updated draft Annex 1 of the EU GMP guidelines on manufacturing of sterile medicinal products. Be sure to read and share your comments before May 20, 2020 as several aspects need the attention of BFS operators. The current proposed draft may be critical to your business so please read and take action now. 

Read more about the consultation at https://ec.europa.eu/health/medicinal_products/consultations/2020_sterile_medicinal_products_en