••• Industry Leaders Celebrate Adeyeye's Push For Production, Affordability
Of Local Medicines
•••To Reposition Nigeria
As Africa’s leading Pharmaceutical Hubs With Global Recognition
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Professor Mojisola Adeyeye, NAFDAC Director-General, received numerous accolades as Sam Pharmaceuticals commissioned a new manufacturing facility in Lagos, signalling the growing impact of regulatory reforms that are increasing local drug production, attracting investment, and positioning Nigeria as one of Africa's leading pharmaceutical hubs.
The commissioning of Sam Pharmaceutical Ltd’s facility was described as a landmark moment for Nigeria’s pharmaceutical industry. The Director General of the National Agency for Food and Drug Administration and Control (NAFDAC), Professor Adeyeye, was the focus of tributes from speakers at the event, who praised her leadership in advancing local manufacturing and strengthening regulatory systems. These include President PSN, Alhaji pharmacist Ayuba Tanko Ibrahim, Registrar PCN, Pharmacist Ahmed Babasheu, Chairman, Fidson Healthcare plc, Mr Fidelis Ayebae, DG. NAFDAC, Prof. Christianah Moji Adeyeye and Chairman, Sam Pharmaceutical Ltd, Mr. Amit Bhojuwani.
Others are the Deputy Governor of Ogun State, Engr. Noimot Salako-Ayodele, Minister of State for Health and Social Welfare, Dr. Iziaq Adekunle Salako, and the Ogun State Commissioner for Health, Dr Oluwatomi Coker.
Leadership And Policy: Driving
Local Production
Professor Adeyeye’s leadership has been
pivotal in reshaping Nigeria’s pharmaceutical landscape. Her “5‑by‑5” policy
requires foreign manufacturers to partner with Nigerian firms or establish
local plants within five years of product registration. This initiative has
already increased domestic production to 50 per cent, up from 30 percent in previous
years.
The impact of this policy is evident in the
strides made by companies such as Sam Pharmaceuticals, which are investing in
local facilities and contributing to national self‑sufficiency in essential
medicines.
International Recognition
Under Professor Adeyeye’s stewardship, NAFDAC has achieved international recognition. In 2022, the World Health Organisation (WHO) awarded Nigeria Maturity Level 3 (ML3) status, confirming that the country’s regulatory system is stable, well‑functioning, and integrated.
This achievement places Nigeria among only
four African nations, alongside Tanzania, Ghana, and Egypt, with effective
regulatory systems at this level. Globally, fewer than 30 percent of regulatory
authorities reach ML3, underscoring the significance of Nigeria’s progress. The
rating also positions NAFDAC to transition into the WHO Listed Authorities, a
group recognised worldwide for meeting international standards.
Benchmarking Journey
Nigeria’s path to ML3 began in 2018 with the WHO Global Benchmarking Programme, which introduced rigorous self‑audits and adherence to international best practices. Following its first audit in 2019, NAFDAC worked consistently to strengthen systems. By February 2022, WHO re‑benchmarked the agency, confirming Nigeria’s attainment of ML3.
This recognition enables Nigeria to
manufacture vaccines and strengthens its credibility in the global
pharmaceutical sector. It also reassures citizens that medicines produced
locally meet stringent safety and efficacy standards.
The 5+5 Policy
The “5+5” policy introduced by Professor
Adeyeye is central to Nigeria’s pharmaceutical reforms. At the point of first
product registration, companies are informed that foreign manufacturers must
either form partnerships with Nigerian firms or establish local plants for
finished pharmaceutical products, active pharmaceutical ingredients, packaging
materials, and more.
Licences are valid for five years. By the
fourth year, companies must submit blueprints of proposed partnerships or local
plants. Renewal depends on verifiable progress. By year seven, if no migration
to local production has occurred, companies face de‑registration
alerts.
For products already renewed multiple times,
immediate blueprints are required. Where a manufacturer has several products, a
plan for at least one is acceptable. This framework ensures a gradual but firm
transition from import dependency to local manufacturing.
Human Impact
Beyond policy and regulation, the reforms
carry a human dimension. Local production reduces import costs, making medicines more affordable. It also ensures greater
availability of life‑saving drugs, particularly in rural areas where shortages
have been common.
For families managing chronic conditions such
as diabetes or hypertension, the promise of reliable supplies is significant.
The commissioning of Sam Pharmaceuticals’ plant reflects this broader national
effort, promising improved healthcare outcomes for millions.
Commendations
At the Lagos event, Professor Adeyeye was
repeatedly commended for her tireless work. Industry representatives noted that
her vision has inspired new investment and positioned Nigeria as a leader in
Africa’s healthcare sector. Her legacy, they said, will be measured not only in
policies but in lives saved and futures secured.
The ceremony also highlighted the importance
of collaboration between regulators, manufacturers, and international partners.
By aligning national policies with global standards, Nigeria is building a
pharmaceutical industry capable of competing internationally while serving
local needs.
Looking Forward
With more local manufacturers emerging,
Nigeria’s pharmaceutical sector is poised for further expansion. The
combination of regulatory strength, policy enforcement, and industry investment
suggests a future where the country can produce not only essential medicines
but also vaccines and advanced therapies.
For Professor Adeyeye, the journey continues.
Her focus remains on strengthening systems, enforcing standards, and ensuring
that Nigeria’s pharmaceutical industry serves its people first. For Nigerians,
the promise is clear: better access, safer medicines, and a healthcare system
increasingly anchored in local innovation.








