We connect African manufacturers with international technology partners to support the local production of active pharmaceutical ingredients (APIs) and finished pharmaceutical products (FPPs), accelerating self-reliance in medicine production.

Our expert-led assessments and audits help companies identify gaps in Good Manufacturing Practice (GMP) compliance. We provide actionable recommendations and hands-on support to build robust Quality Management Systems that align with WHO, US FDA, and EU standards.

We offer customized training programs for pharmaceutical professionals in:

• Quality control and quality assurance

• Analytical methods development and validation

• Formulation development

• Bioavailability/Bioequivalence (BA/BE)

• Regulatory compliance and documentation

Our goal is to develop a skilled local workforce capable of sustaining quality manufacturing operations.

We provide advisory and design support for greenfield pharmaceutical manufacturing facilities, ensuring they meet international design and compliance requirements from inception to commissioning.

We guide companies through national and regional product registration processes across Africa. Our services include:

• Strategic advice on country-specific regulatory pathways

• Pre-submission dossier review

• Compilation support to meet Common Technical Document (CTD) requirements

• Engagement with regulatory authorities to facilitate approvals

Local Expertise, Global Standards: Rooted in Africa, with a leadership team boasting decades of international pharmaceutical experience.

Africa-Focused: We understand the unique regulatory, operational, and infrastructural challenges of the African market and offer practical, tailored solutions.

Quality-Centered: Everything we do is anchored in the commitment to improving the quality of medicines available to African populations.