Home | Sitemap | Contact Us | Login      

National Pharmacy News

Title: Pharmaceutical body commends handling of Hovid product recall
Date: 11-Jan-2017
Category: theedgemarkets.com

Theedgemarkets.com, January 10, 2107

KUALA LUMPUR (Jan 10): The Malaysian Pharmaceutical Society (MPS) has applauded the Health Ministry, National Pharmaceutical Regulatory Agency (NPRA) and Hovid Bhd for their transparency and accountability in addressing Hovid's recent licence revocations.

"All parties acted fast in getting the information to the public," said MPS president Amrahi Buang in a statement today.

He was commenting on the "transparent, efficient and responsible" handling of the recent recall of Ternolol 50 tablets by all three parties, as well as the subsequent cancellation of Hovid's manufacturing licences.

"However, our main concern is the safety of the product user and we hope that all the medication in circulation is returned to Hovid soon," Amrahi said.

Although it would not speculate on the root cause as the investigation is still ongoing, MPS said the society and its members have helped made the message viral on social media with other pharmacists to ensure the recall information was shared widely.

Amrahi said the Malaysian public lack awareness of the regulatory process in the country, adding that the people are not well informed on how to check for registered products and are unclear about recall procedures.

"Due to the lack of understanding, many incorrect assumptions are made and shared on social media in an irresponsible manner," he said.

Nevertheless, he said the NPRA is tasked at ensuring that therapeutic substances approved for the local market are safe, efficacious and of quality via product registration, licensing (manufacture, import and wholesale), monitoring of adverse drug reactions and market surveillance.

Amrahi added that the NPRA only approves a drug registration after it has undergone a stringent screening and approval process of between six and 18 months, depending on the product classification.

Once a drug has been approved, regular post-market surveillance is done to ensure registration compliance.

[ Back ] [ Print Friendly ]

Copyright © 2002 - 2018 Malaysian Pharmaceutical Society. All Rights Reserved.   Web Management