D. I. Medicine Regulatory Consultants has been serving the pharmaceutical industry for the past 20 years and offers a complete range of medicine regulatory services. Our services include compiling and updating of the South African MRF1 and ZA-CTD registration dossiers for human and veterinary orthodox and complementary medicines, including registerable medical devices. We also provide compilation services for registration dossiers of other African countries, as well as compilation of Standard Operating Procedures (SOP), Site Master Files (SMF) and license applications for existing or new applicants. World class auditing services based on current Good Manufacturing Practise (GMP), Good Laboratory Practise (GLP) and Good Wholesale / Warehouse Practise (GWP) are also available. We are also a member of the National Association of Pharmaceutical Manufacturers of South Africa.