FDA intensifies health supplements regulation for consumer safety

By Ma. Teresa Montemayor, Philippine News Agency

The FDA drafted an administrative order (AO) detailing good manufacturing practice and registration requirements for health supplements to foster transparency and industry collaboration. (Pexels Photo)

MANILA – The Food and Drug Administration (FDA) has collaborated with the Health and Dietary Supplement Association of the Philippines (HADSAP) to reinforce regulatory standards and industry compliance for health supplements.

In a news release on Friday, the FDA said it outlined the key points of Southern Cross Initiative and Task Force Thomson during a discussion with the HADSAP.

Both initiatives focus on policy development for traditional medicines and health supplements which are widely used in the country.

The FDA drafted an administrative order (AO) detailing good manufacturing practice and registration requirements for health supplements to foster transparency and industry collaboration.

“This document is open for stakeholder comments on the FDA website, with public consultations scheduled within March,” the FDA said.

Meanwhile, HADSAP sought a comprehensive list of stakeholders, particularly micro, small and medium enterprises (MSMEs), that may qualify for membership.

This move aims to help small and medium enterprises facing challenges in complying with regulatory updates.

The HADSAP, meanwhile, requested the support of the FDA to reinforce its efforts and promote broader industry participation.

The FDA assured the public that it is committed to safeguarding public health while supporting responsible industry growth.

Stakeholders are encouraged to stay informed and participate in the consultation process by visiting the FDA website.