Answer:
If you are a manufacturer of blood- and plasma-derived medicinal products or vaccines and are interested in arranging for OCABR in the EU/EEA, you can request a list at the following address:of potentially suitable OMCLs, which provides an overview of the OMCLs and their competencies, by sending an email to batchrelease@edqm.eu. This list provides an overview only. Direct contact with We strongly recommend contacting the individual OMCLs (refer to question 1) to receive the most up-to-date information with respect to competence and capacity is strongly recommended. For more information, see ‘Where can I find the list of the Official Medicines Control Laboratories (OMCLs) in the EU/EEA currently involved in Official Control Authority Batch Release (OCABR) for human biological medicinal products?’.
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