DI Medicine Regulatory Consultants Information

DI Medicine Regulatory Consultants has been serving the pharmaceutical industry for over 30 years with comprehensive expertise and understanding of the current and ever changing regulatory environment. We offer a complete range of medicine regulatory consulting services throughout South Africa and Africa. Our services include, but are not limited to the regulatory consulting for human medicines, veterinary medicines, medical devices, complementary medicines and cosmetics. We also provide regulatory consulting services for other African countries. We provide assistance with Licence applications and the relevant Quality Management Systems thereof, including Standard Operating Procedures (SOPs), Site Master Files (SMFs), Quality Manuals (QMs) and Pharmacovigilance Management Systems. In addition we assist with GxP preparation by providing world class auditing services based on current Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP) and Good Wholesale/Warehouse Practice (GWP) as required.