Biomanufacturing & Pharma Packaging
In this Issue:
How must CDMOs and packaging suppliers collaborate to deliver compliance with EU serialisation requirements? Which measures must CMOs take now to close the capacity gap? Whatever your business focus is, whether you’re active in facility construction, cell line development/engineering, continious/fed-batch bioprocessing in stainless steel or single use equipment, new vaccine formulations, bioprocess characterisation/documentation/design, process analytics and control, bioequivalence analyses, or downstream processing.
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