Yes. We design and deliver customized technical training programs in fermentation, purification, scale-up operations, and GMP compliance for vaccines, biologics, and bio-based products. Our programs range from operator-level skills training to training-of-trainers courses, and we've successfully trained teams for regulatory authorities, emerging manufacturers, and academic institutions across Africa. All training is tailored to your specific equipment, processes, and regulatory requirements.

Yes. We partner with NGOs, bilateral agencies, and development organizations as training delivery partners, technical advisors, and consortium members. Whether you need bioprocessing curriculum development, regulatory system strengthening, manufacturing capacity assessments, or technical training delivery, we integrate seamlessly into your program design. Our local presence and proven track record with USAID, GIZ, WHO, and Africa CDC projects make us a reliable implementation partner.

Yes. We build regulatory systems through inspector training, assessment framework development, policy advisory, and WHO ML3 certification pathway support. Our programs have strengthened regulatory capacity across multiple African countries including SAHPRA inspectors in South Africa and supporting in Kenya, Rwanda, Ghana, Nigeria, and Senegal. 

Yes. We build regulatory lot release capacity through laboratory training, protocol development, quality control system design, and assessor competency programs. Our support includes establishing testing infrastructure, developing standard operating procedures, training laboratory personnel in batch analysis and documentation review, and creating lot release decision-making frameworks aligned with WHO standards. We've supported regulatory lot release capacity building across multiple African countries through programs