This network is an important forum for the confidential exchange of quality and technical information on human biological medicinal products and related methods and is a key link in the regulatory chain. As mandated by the European Commission, the EDQM acts as its Secretariat. It is a specific network within the General European OMCL Network, thus subject to its operating rules. It is supervised by an elected advisory group consisting of six representatives (three for blood and three for vaccines) from different Member States. A plenary meeting is held annually bringing together all the representatives (their details are available in a contact list) to review the years' activities and to discuss any relevant issues. This meeting also serves as an opportunity to officially adopt the Official Control Authority Batch Release (OCABR) procedures and guidelines, which - like all other OMCL Network activities - must be approved by all the networks' members.
As part of the regulation of biological medicinal products, Article 114 of Directive 2001/83/EC relating to medicinal products for human use, as amended by Directive 2004/27/EC, of the European Parliament and of the Council provides that a Member State laboratory may, but is not required to, test a batch of an immunological medicinal product or a medicinal product derived from human blood or plasma before it is placed on the market. OCABR performed by any given Member State must be mutually recognised by all other member states requiring OCABR for that product.
This legislation concerns EU/EEA Member States and is also applied by any state having signed a formal agreement, which includes recognition of OCABR, with the EU. Currently, Switzerland has done so via a Mutual Recognition Agreement (MRA).
The core administrative procedure for OCABR for Human Biological Medicinal Products is the EU Administrative Procedure For Official Control Authority Batch Release. This is used by OMCLs when implementing OCABR at the national level. It is also intended for use by marketing authorisation holders (MAHs). It provides guidance on documents used for communication between MAHs and OMCLs and describes the steps involved in the OCABR process, which are summarised below:
The Member State informs the MAH that its authorised human biological medicinal product is subject to OCABR. Samples of the batch to be released are sent, along with production and control protocols, to an OMCL within the EU/EEA. If the results are satisfactory, the Competent Authority (CA) issues an 'Official Control Authority Batch Release Certificate' to the MAH. This certificate means that the batch has been examined and tested by an OMCL in accordance with the OCABR guidelines pertaining to the medicinal product and is in compliance with the approved specifications laid down in the relevant monographs of the European Pharmacopoeia and in the relevant marketing authorisation (MA). The MAH must provide a copy of the OCABR Certificate to the Competent Authority (CA) of the Member State where the batch will be marketed. The certificate is recognised by all members of the network.
If the results are unsatisfactory, the batch is given a certificate of non-compliance and may not be placed on the market. All members of the OCABR network are informed.
In addition to the Administrative Procedure, there is a series of product specific guidelines. These are elaborated by a panel of experts from various OMCLs under the aegis of the EDQM. These documents facilitate OMCLs in meeting the requirements of Directive 2001/83/EC, as amended by Directive 2004/27/EC. They ensure a common approach to testing in all OMCLs throughout the EU/EEA and transparency for all users of the system. The guidelines are adopted only after consultation within the network and where appropriate after a public enquiry involving interested parties.
The procedures and guidelines for running OCABR apply equally in all Member States.
OCABR guidelines and procedures are available exclusively on our website. The complete list is presented in a table from which the files may be downloaded. The guidelines will be updated on an on-going basis as needed. New and revised versions will be placed on the website within one month of their date of entry into force. Users are encouraged to visit the site regularly to ensure they are using the most recent versions. Highlights on recent addition and revision updates can be found in the right-hand menu.
To download all product specific guidelines and procedures, please go to the "Guidelines for EU Official Control Authority Batch Relase for Human Biological Medicines" webpage.
In force from 1st August 2015
- Explanatory Note on Correct
Application of Section 3.2 of Product
Specific Guidelines for Official Control
Authority Batch Release
- Clotting factor Concentrates, Plasma
Inhibitor Concentrates and Fibrin Sealants
In force from 1st June 2015
- Hepatitis A (Virosomal) Vaccine
- Live Attenuated Influenza Vaccine
In force from 1st February 2015
- Diphtheria, Tetanus, Pertussis
(Acellular Component), Poliomyelitis
(Inactivated) and Haemophilus Type B
Conjugate Liquid Combined Vaccine
- Diphtheria, Tetanus and Pertussis
(Acellular Component) Combined
- Vaccine Containing Vaccinia Virus
Produced In Cell Culture (Smallpox
In force from 1st January 2015
- Human Immunoglobulin
- Human Plasma (pooled and treated
for virus inactivation) formerly Solvent-
Detergent (SD) Plasma
- Protocol for Approval of Plasma Pools
- Haemophilus Type B Conjugate
- Monovalent or Multivalent
Meningococcal Conjugate Vaccine
- Multivalent Pneumococcal
Polysaccharide Conjugate Vaccine
In force from 1st September 2014
- Meningococcal B Vaccine (Adsorbed)
(revised December 2010)