DI Medicine Regulatory Consultants

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...

Pharmaceutical regulatory ,medical devices,complementary medicines,biological medicines,veterinary medicines,act 101 medicine registrations,dalrrd applications,licencing,quality management systems,gxp audits,pharmaceutical labeling,new chemical entities,biosimilars,common technical dossiers (ctd),africa regulatory submissions,pharmacovigilance,artwork/advertisements translations and proofreading,cosmetics,protocol management,due diligence,regulatory management,dossier lifecycle management,ectd,and document management system (docubridge)

Di medicine regulatory consultants operates in the Pharmaceutical manufacturing industry.

Di medicine regulatory consultants's revenue is 11m - 100m

Di medicine regulatory consultants has 11 - 50 employees.