The Directives/Guidelines listed below represented the minimum standards by which EMVI conducts all its operations.
All entities with whom EMVI enteres into contractural agreements, partnerships, or otherwise collaborates and has dealings, is expected to adhere to the standards laid down in the following:
Commission Directive 2003/94/EC of 8 October 2003 Laying down the principles and guidelines of Good Manufacturing Practice (GMP) in respect of medicinal products for human use and investigational medicinal products for human use.