FDA reviews its processes to enable local cosmetics manufacturers to register products

FDA reviews its processes FDA reviews its processes

The Food and Drugs Authority (FDA) is urging local manufacturers of cosmetics and household chemical substances to register with the Authority.

Over the years, only a few start-ups were able to register their products at the FDA due to the challenges they encountered during the registration process, as well as inherent difficulties in meeting regulatory requirements prior to market authorization.

As part of efforts to solve this problem, the Authority has put in place some measures to make it easier for small and medium scale enterprises to legalise their businesses and products.

The Head of the Cosmetics and Household Chemicals Department of the Authority, Emmanuel Nkrumah, speaking to Citi News, stated that, "We will have to get more locally manufactured products on our markets to the best of our ability. How do we do that? We've reviewed our forms. During the stakeholder interaction and engagement, we got feedback from our stakeholders that the forms are too complicated. What can be done? If that is what the stakeholders are saying, then it's something to have a second look at. So we've reviewed our forms to make them simpler than they used to be."

He continued, "And we also have a different approach with regard to how we meet and engage our clients. Now we have a very efficient and reliable client service that is monitored on a daily basis. And we also gave a very good fee schedule. Now the fee for locally manufactured products is in categories. We have the small, medium and large scale. The fee for small-scale businesses is GH¢300 per product. And in some instances, we even grouped them and put one or two products together and charge GH¢300, which is about GH¢100 per year. That comes to about GH¢8.30 a month, which amounts to nothing."

The Food and Drug Authority is mandated by the Public Health Act, 2012 (Act 851) to regulate food, drugs, food supplements, herbal and homeopathic medicines, veterinary medicines, cosmetics, medical devices, household chemical substances, tobacco and tobacco products as well as clinical trials.

In an earlier statement, it stated that it had "recognized the financial challenges associated with start-up business projects and the inherent difficulties in meeting regulatory requirements prior to market authorization".

It has thus "outlined a number of measures to address the various industry growth-enabling provisions available to small and medium scale enterprises in Ghana".

According to them, these new measures are in support of various government initiatives like the One District, One Factory (1D1F), and other small-scale industries.

Source: By Ellen Dapaah