The incident raises serious questions regarding the methods used by the Pakistan Pharmaceutical Manufacturing Industry (PPMI) for quality assurance purposes. While all raw materials used in pharmaceutical manufacturing are supposed to undergo proper testing before their release for commercial production, it appears as if our pharmaceutical industry does not have any mechanism for a verification of its own, and solely relies on the Certificate of Analysis issued by the supplier. This puts the lives of unsuspecting patients at serious risk and has surprisingly gone undetected by the regulatory authorities until a voluntary disclosure by the EMA.
Even more surprising is the fact that after several weeks of the EMA alert, physical recall of the products containing the contaminated raw material is yet to start and the same continues to occupy the shelves at drug stores and continues to be prescribed by doctors as well. In more developed and regulated markets, such actions are taken jointly and responsibly by the industry as well as the regulators to ensure patient safety. Timely notice of the issue is of utmost importance as it is a matter involving public health and precious lives.
Published in The Express Tribune, July 21st, 2018.
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