FDA RFO III

Training on the Registration Process and Post-Approval Changes of Pharmaceutical Products for Human Use by the Center for Drug Regulation and Research (CDRR)

This three-day training will provide detailed discussions of the technical requirements and procedures on the issuance of Certificate of Product Registration (CPR) including Post-Approval Changes of pharmaceutical products for human use.

Join our face-to-face training on 08-10 July 2026 from 8:00 am to 5:00 pm

Venue: Vivere Hotel, Alabang, Muntinlupa City
Registration fee: Php 8,500.00
Register through this link: bit.ly/4v8sGZy

Maximum of 70 participants
First-come-first served basis

All successful registrants/applicants shall wait for the confirmation email from the FDA Academy for the issuance of Course Assessment Slip (CAS) and payment instruction pursuant to FDA Circular 2023-010.

Payments made without the corresponding CAS from the FDA Academy shall be forfeited.

Training on Licensing of Medical Device Establishment and Product Registration (MDLPR)

This three-day training will provide detailed discussions of the procedural issuance of License to Operate (LTO) for Medical Device Establishments and the Requirements in securing a Certificate of Medical Device Registration (including In Vitro Diagnostics) and other Health-Related Devices and to provide orientation on the process of submission of each application to the Center for Device Regulation, Radiation Health, and Research

Join our face-to-face training on 14-16 July 2026 from 8:00 am to 5:00 pm

Venue: Vivere Hotel, Alabang, Muntinlupa City
Registration fee: Php 8,500.00
Register through this link: bit.ly/3S222TO

Maximum of 70 participants
First-come-first served basis

All successful registrants/applicants shall wait for the confirmation email from the FDA Academy for the issuance of Course Assessment Slip (CAS) and payment instruction pursuant to FDA Circular 2023-010.

Payments made without the corresponding CAS from the FDA Academy shall be forfeited.

Training on the Issuance of License to Operate, Food Product Registration Procedure and Other Authorizations and Core Processes

This three-day training program by the FDA Center for Food Regulation and Research (CFRR) aims to provide stakeholders detailed information on regulatory requirements and procedures for securing FDA-CFRR market authorizations (e.g., License to Operate, Certificate of Product Registration (CPR), Sales and Promo Permit, Import Permit).

This training will also cover an overview of the Food Safety Act of 2013, highlighting the following: 1) roles and responsibilities of Food Business Operators, 2) specific Post-marketing Surveillance activities being conducted by the FDA-CFRR, and 3) handling and evaluation of consumer complaints and other reports from government agencies and industry.

Join our face-to-face training on 29-31 July 2026 from 8:00 am to 5:00 pm

Venue: Vivere Hotel, Alabang, Muntinlupa City
Registration fee: Php 8,500.00
Register through this link: bit.ly/4e4hfMQ

Maximum of 70 participants
First-come-first served basis

All successful registrants/applicants shall wait for the confirmation email from the FDA Academy for the issuance of Course Assessment Slip (CAS) and payment instruction pursuant to FDA Circular 2023-010.

Payments made without the corresponding CAS from the FDA Academy shall be forfeited.

𝐏𝐑𝐎𝐂𝐋𝐀𝐌𝐀𝐓𝐈𝐎𝐍 𝐍𝐎. 𝟏𝟐𝟔𝟒, 𝐬. 𝟐𝟎𝟐𝟔

Declaring Wednesday, 27 May 2026, a Regular Holiday Throughout the Country, in observance of Eid'l Adha (Feast of Sacrifice)

Visit the Official Gazette website: https://www.officialgazette.gov.ph/RJdUhv

Training on Good Manufacturing Practice for Food Manufacturers and Traders (GMP-FMT)

This webinar will provide the methods, identify the equipment, enumerate the facilities, and determine the controls for producing processed food as stated in the Current GMP for Food, as published in A.O. 153 s 2004..

Join our webinar on 23-24 July 2026 from 8:00 am to 5:00 pm via Google Meet
Registration fee: Php 800.00
Register through this link: bit.ly/4stACmu

Maximum of 1000 participants
First-come-first-served basis

All successful registrants/applicants shall wait for the confirmation email from the FDA Academy for the issuance of Course Assessment Slip (CAS) and payment instruction pursuant to FDA Circular 2023-010.

Payments made without the corresponding CAS from the FDA Academy shall be forfeited.

***FDA Advisory No.2026-0358 || Pilot Implementation of e-Services for Registration Applications of Processed Food Products under Center for Food Regulation and Research (CFRR)***

The Food and Drug Administration (FDA) informs all concerned stakeholders that, following the successful completion of the pilot testing phase of the e-Services for registration applications of processed food products, a three-month pilot implementation shall be conducted from 16 February 2026 to 15 May 2026. This pilot implementation shall cover the following types of applications:

See more:-> https://tinyurl.com/rkuacn4v