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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 of potentially suitable OMCLs, which provides an overview of the OMCLs and their competencies, by sending an email to We strongly recommend contacting the individual OMCLs to receive the most up-to-date information with respect to competence and capacity. 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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