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PAMDRAP: Architects of Regulatory Excellence

Welcome to the beating heart of transformative change in the Philippine medical device landscape – the About Us page of the Philippine Association of Medical Device Regulatory Affairs Professionals, affectionately known as PAMDRAP. We’re not just an association; we are the architects of regulatory excellence, the pioneers shaping the future of medical device regulations in the Philippines.

Who We Are

PAMDRAP stands for Philippine Association of Medical Device Regulatory Affairs Professionals. It is a
non-stock and non-profit association composed of regulatory affairs professionals representing medical
device companies. It is recognized by the Center for Device Regulation, Radiation Health and
Research.

Our Vision

To uplift the Medical Device Industry by organizing and uniting regulatory affairs professionals and by
acting as a dialogue partner and resource of appropriate government agencies in the seamless
implementation of Medical Device Regulations in the Philippines.

About Us

PAMDRAP stands for Philippine Association of Medical Device Regulatory Affairs Professionals. It is a
non-stock and non-profit association composed of regulatory affairs professionals representing medical
device companies. It is recognized by the Center for Device Regulation, Radiation Health and
Research.
PAMDRAP is a spin-off of the Medical Device Task Force of the Philippine Association of Pharmacists in
the Pharmaceutical Industry (PAPPI). The association was registered and incorporated with the
Philippine Securities and Exchange Commission in September 8, 2011.

Why We're Here

Our Purpose

At PAMDRAP, we unite Regulatory Affairs Professionals in the Philippine Medical Device industry. Our goal is to facilitate collaboration with government agencies, empower members through training and support, disseminate crucial information, and partner with regulatory bodies to ensure compliance with medical device regulations.

1

To organize and unite all Regulatory Affairs Professionals of the Medical Device industry in the Philippines and act as a dialogue partner and resource of appropriate government agencies in the implementation of medical device regulations.

2

To enable and empower Regulatory Affairs Professionals in fulfilling their critical role as regulatory compliance officer in each individual companies by providing support system among membership through structured medical device trainings, sound and practical advise or experience-sharing on registration issues and guidance on identifying appropriate government agencies or contacts to deal with.

3

To function as a conduit for the dissemination of information to industry members and undertake detailed study group activities or deliberate technical issues, leading to recommendations for feedback or actions in the preparation of regulatory policies, where applicable.

4

To partner with appropriate regulatory bodies and industry associations in carrying out capacity building programs for regulators and industry members, in the various initiatives and objectives in order to promote common understanding of regulatory requirements.

1

To organize and unite all Regulatory Affairs Professionals of the Medical Device industry in the Philippines and act as a dialogue partner and resource of appropriate government agencies in the implementation of medical device regulations.

2

To enable and empower Regulatory Affairs Professionals in fulfilling their critical role as regulatory compliance officer in each individual companies by providing support system among membership through structured medical device trainings, sound and practical advise or experience-sharing on registration issues and guidance on identifying appropriate government agencies or contacts to deal with.

3

To function as a conduit for the dissemination of information to industry members and undertake detailed study group activities or deliberate technical issues, leading to recommendations for feedback or actions in the preparation of regulatory policies, where applicable.

4

To partner with appropriate regulatory bodies and industry associations in carrying out capacity building programs for regulators and industry members, in the various initiatives and objectives in order to promote common understanding of regulatory requirements.

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