FDA TO GET TOUGH WITH INDUSTRY
The Food and Drugs Authority, FDA is to enforce Section 106 of the Public Health Act which mandates all food processing industries to have at least one qualified food scientist or food microbiologist on their payroll, to handle and oversee delicate aspects of their food processing system.
Such personnel will be mandated to periodically share their
laboratory test results with the FDA and in the event of any fraudulent or
negligent act, will be held liable, with the possibility of the individual also
losing their certificate.
The Regulatory
Officer at the Food and Drugs Authority, P. A. Opoku announced this at a forum
in Kumasi.
He said the Authority as a matter of urgency, intends to launch a
programme which will regularize free sampling of locally manufactured
consumables on the market from such small scale industries.
However, this will
require funds to be allocated for the laboratory tests.
Mr. Opoku said in an
attempt to encourage and motivate consumers to readily report fraudulent food
practices, plans are far advanced to make the FDA help line a toll free line.
Management of the Authority also anticipates creating social platforms and a link
on the FDA website to facilitate food fraud reportage.
He explained that a
fundamental requirement to arrest the food fraud menace is to protect the
consumer from food crime.
This can be achieved through improvements to
intelligence gathering, information sharing, monitoring the traceability of
food ingredients and improved food fraud detection methods.
Mr. Opoku said the
FDA will undertake frequent visits to small scale industries for standards to
be introduced and implemented within a short period of time, after which
supervision and appropriate sanctions can be taken against offenders.
He noted
that one of the fastest ways of detecting fraudulent food products on the
market id the use of rapid test kits.
Mr. Opoku therefore asked research
institutions, academia and all stakeholders to come up with rapid test kits to
help FDA in identifying adulterated food products on the market.
He explained
that these test kits, compared to the traditional method of sampling from the
field and analyzing later in the laboratory, will enable officers of the FDA to
take appropriate regulatory decision right on the field.
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