Advisory Services

Getting a new pharmaceutical product approved doesn’t have to be slow or stressful. We manage the entire registration process with the Tanzania Medicines and Medical Devices Authority (TMDA) and other relevant bodies, ensuring every submission meets the highest standards of quality and compliance.

Opening or upgrading a pharmaceutical manufacturing facility, warehouse, or distribution center requires flawless regulatory alignment. We guide you through the entire site registration and Good Manufacturing Practice (GMP) certification journey.

Regulatory obligations don’t end with approval. We help you maintain full compliance throughout the product lifecycle so your medicines and devices remain legally marketable without interruption.

We offer a wide range of additional services designed to address the unique challenges faced by pharmaceutical businesses in Tanzania and across East Africa.