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Doctor's Desk


Bispharm Clinical is a leading clinical research Site Management Organisation (SMO) based in Nigeria. We are committed to helping Sponsors, Contract Research Organisations (CROs), and Clinical Trial Sites achieve their goals in a timely and cost-effective manner. Our unique approach to clinical trial management ensures that your project is always on track, and the results are reliable and actionable. With Bispharm Clinical, you can count on a successful and smooth clinical trial experience.


We partner with local and global research institutions, private institutions, government agencies, biotechnology and pharmaceutical companies to bring effective treatment options to patients in urban, rural and hard-to-reach communities across Nigeria and West Africa. Our team is made up of dedicated professionals who have been collaborating with researchers, clinical trial sites, sponsors, and CROs for decades. 


We provide exceptional clinical trial site management services including patient recruitment, regulatory compliance and management, clinical monitoring, clinical data management, pharmacovigilance etc. Our team includes project managers, clinical research associates, regulatory affairs managers, and data managers. We work together to ensure that every clinical trial we manage is conducted efficiently and effectively.


We are dedicated to promoting and streamlining ICH-GCP-compliant clinical trials of drugs, vaccines and medical devices. We promise to expand therapeutic access to a broader range of patient populations through innovative management of clinical trials. 


We value transparent and collaborative partnerships with clinical research sites, sponsors, and other stakeholders. This involves open communication, mutual respect, and a shared commitment to success. 


All our services are tailored to uphold a moral obligation to act for the benefit of others, including our patients. Our core tenet at Bispharm is hinged on developing new scientific knowledge for societal benefit.

Diversity and Inclusion 

We operate within an environment where stakeholders, partners and study participants are valued and respected, regardless of their background, ethnicity, race, gender, religion, or other differences. 

Patient Centricity

We recognise that patients are the heart of clinical trials. For this reason, we are committed to ensuring their safety, comfort, and well-being by interfacing with them regularly to gain insights into how they could be served better. 


We are committed to the highest standards of ethical behaviour in all aspects of our operations. This includes adhering to industry best practices of privacy and confidentiality of clinical data of study participants.

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