The National Agency for Food and Drug Administration and Control, NAFDAC, says the World Health Organisation, WHO, has upgraded the agency to maturity level three in drug regulations and others.
The NAFDAC Director-General, Prof. Mojisola Adeyeye, disclosed this at a news conference on Wednesday, in Abuja.
Mrs Adeyeye said that the journey of attaining the status all began January 2018, five weeks after her resumption as the director-general of the agency, and that the agency went through a lot of tasks before it could attain maturity level three.
He said that she got to know about the news at about 1 a.m on Wednesday and she immediately broadcast the news via e-mail to some relevant government personalities.
“The agency has earlier been told sometime in 2018 that it needed to meet up with 868 recommendations before it can get to maturity level three, and the agency immediately step-up work on the process.
“WHO Global benchmarking is all about comparing regulatory agencies that work to carry out tasks pertaining to the best health regulatory agency in the world, it is not about comparing ourselves with ourselves but with the best.
“And, they told us that we need to meet up with 868 recommendations before we can get to maturity level three, it sounded impossible but my directors stood by me all the way,” she said.
According to her, there is a group of people in NAFDAC, we call them the Global Benchmarking team, and they have sacrificed a lot, they are the one that were marking whichever recommendations we have met.
“In June 2019, WHO came to NAFDAC physically to start the benchmarking process and out of the 868 recommendations, we were able to make over 600 and we have 147 left up till June 2019, but those 147 that were left were the most difficult ones.
“We started working at it with retreat, with training because it is all about training, one thing we also did in parallel making sure NAFDAC is built on a quality system is `quality management system’, it was it that got us to the 147 recommendations left in 2019.
“We continue in that direction, but in July 2021, WHO met us virtually and we were able to reduce the 147 to 33, the 33 were the most difficult, our staff work endless hours, I thank them, may I also use this medium to thank the council for recommending regulations, they work tirelessly,’’ she said.
Mrs Adeyeye said that with 33 tasks of recommendations left, WHO came back in October 2021, and by then the agency was able to clear all the remaining recommendations, and was waiting for it to re-bench mark the agency.
She said that WHO also came between Feb. 21 and Feb. 25 for re-bench marking the agency, and the information was finally broken to the agency today (Wednesday).
According to her, global benchmarking requires about eight functions that must be performed to the satisfaction of WHO among which is licensing and inspection.
She stated that through-out the journey of attaining this present status, the Pharmacists Council of Nigeria (PCN) was rightly behind the agency because it stood a prime position in ensuring the licensing of pharmaceutical companies before they can start operating.
She said that without NAFDAC and PCN, Nigeria would be filled with substandard and falsified medicine, adding that PCN did a lot of downstream functions in checking for substandard.
Mrs Adeyeye stated that the agency would work further to ensure it attained level four (4) maturity status, and thanked President Muhammadu Buhari for the confidence reposed in her to work for her mother land.
Yusuf Suleiman, Chairman, NAFDAC Governing Board, also appreciated the impact played by the government, adding that government support had made the agency to strengthen its regulatory capacity.
