Comprehensive legal counsel for hospitals, pharmaceutical companies, healthcare providers, and regulatory bodies navigating Nigeria's complex health sector landscape.
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The healthcare and pharmaceutical industry operates at the intersection of science, commerce, and regulation. At Worldwide Solicitors, our dedicated practice group advises hospitals, clinics, pharmaceutical manufacturers, medical device companies, and health insurers on the full range of legal matters arising from their operations in Nigeria and across Africa.
We understand the unique pressures of the health sector — from NAFDAC licensing and NHIS compliance to product liability and clinical trial agreements. Our lawyers work closely with technical and regulatory experts to provide advice that is not only legally sound but operationally practical for healthcare businesses.
Whether you are a multinational pharmaceutical company seeking market authorisation, a hospital facing a clinical negligence claim, or a health-tech startup navigating data protection requirements, we bring the specialist expertise needed to protect your interests and advance your objectives.
What We Handle
Product registration, licensing, import permits, and ongoing compliance with NAFDAC regulations for pharmaceuticals, food, and medical devices.
Drafting and negotiating clinical trial agreements, ethics committee submissions, and regulatory approvals for pharmaceutical research in Nigeria.
Obtaining operational licences for hospitals, clinics, diagnostic centres, and specialist facilities from federal and state health authorities.
Defending pharmaceutical and medical device manufacturers against product liability claims and recall-related litigation before Nigerian courts.
Advising HMOs and health insurers on NHIA accreditation, policy compliance, and disputes with healthcare providers and enrollees.
Representing healthcare providers in clinical negligence claims and advising on risk management frameworks to minimise liability exposure.
Supply agreements, distribution contracts, licensing deals, and co-promotion arrangements throughout the pharmaceutical supply chain.
Patient data protection, NDPR compliance for health records, and data sharing agreements between healthcare organisations.
Our Methodology
We begin by mapping every applicable regulatory obligation — from NAFDAC and NHIA to state-level requirements — so nothing is overlooked before you commence operations.
We design the optimal pathway for obtaining all required authorisations, coordinating submissions and liaising with regulators on your behalf to minimise delays.
Our team drafts sector-specific agreements and internal compliance programmes tailored to the operational realities of healthcare businesses in Nigeria.
When enforcement action or litigation arises, we deploy our litigation and regulatory teams to defend your interests swiftly and decisively.