PANDRH Network Secretariat

The PANDRH Secretariat, served by the Pan American Health Organization, provides technical and administrative support to all components of the Network, including the Pan American Conference, the Steering Committee, and the technical structures. It facilitates the coordination, communication, and follow-up of the Network’s activities, supporting the implementation of the Conference’s recommendations, the Steering Committee’s decisions, and initiatives aimed at strengthening regulatory systems and promoting regulatory harmonization and convergence in the Region of the Americas.

The Secretariat also represents PANDRH in global and interregional regulatory harmonization and convergence initiatives, such as ICH, IMDRF, IPRP, and ICDRA, in coordination with the Steering Committee and the national regulatory authorities of the Region. This participation helps strengthen the Region’s engagement in international regulatory processes, promote the exchange of good practices, and facilitate alignment with global standards and approaches relevant to regulatory convergence.

Functions of the Secretariat of the PANDRH Network

Organize and Coordinate

The network's conferences in coordination with the Executive Commitee and host countries.

Support Technical Cooperation

with the national regulatory authorities to strengthen regulatory convergence in the region.

Communicate and disseminate

information, technical documents and educational material.

Represent the PANDRH Network

in international initiatives on pharmaceutical harmonization and regulation.

Maintain up-to-date records

of members, projects, and strategic areas.

Support financial management

and the preparation of annual results reports.

Related links

Imagen 1

International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH)

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Imagen 2

International Medical Device Regulators Forum

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Imagen 3

International Coalition of Medicines Regulatory Authorities (ICMRA)

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Imagen 4

International Conference of Drug Regulatory Authorities (ICDRAs)

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