EC - New Zealand MRA
The Sectoral Annexes on Medicinal products GMP Inspection and Batch Certification to the MRA in relation to conformity assessment, certificates and markings between the European Community and New Zealand (OJ L229 on 17/08/1998) are in operation since 1 January 1999 for human medicinal products.
The agreement is based on exchange of certificates for manufacturers and batches. The contents of these certificates have been agreed with New Zealand. A Two Way Alert System based on the European system is in operation. For veterinary medicinal product the operational phase started on 1 June 2002.
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