Regulatory Affairs Consultants. Compilation of NCE and generic CTD dossiers for medicines in South Africa and English speaking African countries. Compliance with legislative requirements to hold applicancy for product dossiers

MedReg Consultants are strategic outsourcing partners to the pharmaceutical and allied health care industries in Southern Africa offering professional support to the pharmaceutical and related industries.

MRA Regulatory Consultants was established in 2003 to provide expert Regulatory Affairs & advisory services and regulatory support services to the Pharmaceutical Industry. We enjoy a clear understanding of the regulatory environment in South Africa, its history, trends, current requirements and policies.

Registrar Corp provides U. S. FDA compliance assistance to companies in the food and beverage, medical devices, cosmetics, drug, and tobacco industries.

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.

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.