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Addressing Annex I

Download the latest De Lama e-book to uncover their solutions to overcoming Annex I challenges.

In this e-book De Lam shares how its innovative technology and design complies with the latest EU GMP requirements in respect of Annex I, such as barrier technology, disinfection, equipment & sterilisation.

“It is immediately clear how the focus, moving from sterile medicines to sterile products, extends the scope of application of the standard also to active substances, sterile excipients, primary packaging materials and finished dosage forms, processes (from highly automated systems to manuals) and technologies applied to the production of "small molescules" and biotechnological products.”


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