DI Medicine Regulatory Consultants has been serving the pharmaceutical industry for over 25 years and offers a complete range of medicine regulatory services. Our services include compilation and updating of CTD and eCTD registration dossiers for human and complementary medicines. 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.