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The Policy and Planning Service – FDA Academy announces the following seminar/training offerings for the 2nd Quarter of CY 2024 through online video-conferencing platform and face-to-face learning to be held within Alabang, Muntinlupa City (venue to be announced) and may include additional program as the need arises:

Title of Training/Seminar Center Responsible Program Description Schedule Course Code Mode of Delivery Registration Fee
JULY
Training on 13 Modules of ASEAN Good Manufacturing Practices for Cosmetic Manufacturers and Traders Field Regulatory Operations Office (FROO) The program provides a detailed discussion on the ASEAN Guidelines for Cosmetic Good Manufacturing Practice (GMP). 17-18 July 2024 GMP-CMT Face-to-Face ₱6,500.00
Training on Medical Device Product Registration Center for Device Regulation and Radiation Health Research (CDRRHR) The course aims to discuss the Legal and Technical Requirements in securing a Certificate of Product Registration for Medical Devices (including IVDs) and other Health-Related Devices and to provide orientation on the process of submission of application. 23-24 July 2024 MDPR Face-to-Face ₱6,500.00
Training on Globally Harmonized System of Classification and Labelling of Chemicals (GHS) for Stakeholders Center for Cosmetics and Household/Urban Hazardous Substances Regulation and Research (CCHUHSRR) The program provides detailed discussion on the application of GHS in classifying HUP/HUHS products in terms of their physical, health and environmental hazards and communicating these hazards using Safety Data Sheets and the harmonized GHS label elements. 29 July – 02 August 2024 GHS-CLC Face-to-Face ₱16,000.00
AUGUST
Training on PIC/S GMP Guide PE 009-14: Current Regulatory Requirements Field Regulatory Operations Office (FROO) The program provides discussion of the provisions stipulated in the current version (ver. 14 of the PICS GMP Guide) and other regulatory requirements to comply with Good Manufacturing Practice for Pharmaceuticals. 07-08 August 2024 PIC/S-GMPCRR Face-to-Face ₱6,500.00
Training on Food Product Registration and Other Authorizations and Core Processes Center for Food Regulation and Research (CFRR) A two-day program for FDA Center for Food Regulation and Research stakeholders aims to provide detailed information on regulatory requirements and procedures for securing FDA-CFRR market authorizations (e.g., 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 roles and responsibilities of Food Business Operators, specific Post-marketing Surveillance activities being conducted by the FDA-CFRR, and handling the evaluation of consumer complaints and other reports from government agencies and industry.

13-14 August 2024 TFPR-ACP Face-to-Face ₱6,500.00
Training on Medical Device Product Registration Center for Device Regulation and Radiation Health Research (CDRRHR) The course aims to discuss the Legal and Technical Requirements in securing a Certificate of Product Registration for Medical Devices (including IVDs) and other Health-Related Devices and to provide orientation on the process of submission of application. 15-16 August 2024 MDPR Face-to-Face ₱6,500.00
Licensing Seminar for Pest Control Operator (PCO) Establishments Center for Cosmetics and Household/Urban Hazardous Substances Regulation and Research (CCHUHSRR) This seminar is intended for all Pest Control Operators (PCO) engaged in the application of household/urban pesticides (HUP) or any other methods/services for pest control. Participants may be owners/ general managers/ authorized representatives of PCO establishments, as well as supervising pesticide handlers, and pesticide handlers.

The aim of this training is to gain knowledge on the implementing guidelines of DOH A.O. No. 2019-0010 on the Issuance of a License to Operate (LTO) as a Household/Urban Pest Control Operator.

Topics include LTO requirements, demonstration of LTO application as a PCO establishment via the FDA eServices Portal, inspection requirements and responsibilities of PCO establishments, supervising pesticide handlers, and pesticide handlers among others.

20 August 2024 LS-PCO Webinar FREE
Training on Technical Requirements and Regulatory Guidelines for Cosmetics Products Center for Cosmetics and Household/Urban Hazardous Substances Regulation and Research (CCHUHSRR) The program provides a detailed and procedural discussion on technical requirements and process for cosmetic product notification. 22-23 August 2024 TR-RGCP Face-to-Face ₱6,500.00
Training on CDRR Registration Process Center for Drug Regulation and Research (CDRR) The program provides detailed discussions on the technical requirements and procedures for the issuance of Certificate of Product Registration (CPR) and other authorization for pharmaceutical products for human use. 27-28 August 2024 CDRR-RP Face-to-Face ₱6,500.00
Training on 13 Modules of ASEAN Good Manufacturing Practices for Cosmetic Manufacturers and Traders Field Regulatory Operations Office (FROO) The program provides a detailed discussion on the ASEAN Guidelines  for Cosmetic Good Manufacturing Practice (GMP). 29-30 August 2024 GMP-CMT Face-to-Face ₱6,500.00
SEPTEMBER
Training on Globally Harmonized System of Classification and Labelling of Chemicals (GHS) for Stakeholders Center for Cosmetics and Household/Urban Hazardous Substances Regulation and Research (CCHUHSRR) The program provides detailed discussion on the application of GHS in classifying HUP/HUHS products in terms of their physical, health and environmental hazards and communicating these hazards using Safety Data Sheets and the harmonized GHS label elements. 02-06 September 2024 GHS-CLC Face-to-Face ₱16,000.00
Training on Technical Requirements and Regulatory Guidelines for Household Urban Pesticide Products Center for Cosmetics and Household/Urban Hazardous Substances Regulation and Research (CCHUHSRR) The program provides technical assistance to concerned stakeholders on the rules and regulations in the registration of household pesticide products and their active ingredients as well as other regulatory matters applicable for pesticide products. 11-12 September 2024 TR-HUPP Face-to-Face ₱6,500.00
Licensing Seminar for Food Establishments Center for Food Regulation and Research (CFRR) A licensing seminar for FDA Center for Food Regulation and Research stakeholders which aims to provide information on the Rules and Regulations prescribing the requirements and procedures in the application for License to Operate for food manufacturers, repackers, traders, distributors, importers, exporters and wholesaler. The topics include the requirements, procedure for Eportal and Eservices Portal Systems covering the initial, renewal and variation application; as well as the schedule of fees and processing time. 18 September 2024 LS-F Online Platform FREE
Training on Technical Requirements and Regulatory Guidelines for Cosmetics Products Center for Cosmetics and Household/Urban Hazardous Substances Regulation and Research (CCHUHSRR) The program provides a detailed and procedural discussion on technical requirements and process for cosmetic product notification. 24-25 September 2024 TR-RGCP Face-to-Face ₱6,500.00
Training on Good Manufacturing Practices for Food Manufacturers and Traders Field Regulatory Operations Office (FROO) The program provides a description of the methods, equipment, facilities, and controls for producing processed food as stated in the Current Good Manufacturing Practices for Food, as published in A.O. 153 s 2004. 26-27 September 2024 GMP-FMT Face-to-Face ₱6,500.00
OCTOBER
Training on CDRR Registration Process Center for Drug Regulation and Research (CDRR) The program provides detailed discussions on the technical requirements and procedures for the issuance of Certificate of Product Registration (CPR) and other authorization for pharmaceutical products for human use. 02-03 October 2024 CDRR-RP Face-to-Face ₱6,500.00
Training on Technical Requirements and Regulatory Guidelines for HUHS Products Center for Cosmetics and Household/Urban Hazardous Substances Regulation and Research (CCHUHSRR) The program provides detailed discussions on the technical requirements and procedure for the issuance of Certificate of Product Registration (CPR) for Categories III and IV HUHS Products. 09-10 October 2024 TR-HUHSP Face-to-Face ₱6,500.00
Training on Medical Device Product Registration Center for Device Regulation and Radiation Health Research (CDRRHR) The course aims to discuss the Legal and Technical Requirements in securing a Certificate of Product Registration for Medical Devices (including IVDs) and other Health-Related Devices and to provide orientation on the process of submission of application. 15-16 October 2024 MDPR Face-to-Face ₱6,500.00
Training on Food Product Registration and Other Authorizations and Core Processes Center for Food Regulation and Research (CFRR) A two-day program for FDA Center for Food Regulation and Research stakeholders aims to provide detailed information on regulatory requirements and procedures for securing FDA-CFRR market authorizations (e.g., 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 roles and responsibilities of Food Business Operators, specific Post-marketing Surveillance activities being conducted by the FDA-CFRR, and handling the evaluation of consumer complaints and other reports from government agencies and industry.

17-18 October 2024 TFPR-ACP Face-to-Face ₱6,500.00
Training on PIC/S GMP Guide PE 009-14: Current Regulatory Requirements Field Regulatory Operations Office (FROO) The program provides discussion of the provisions stipulated in the current version (ver. 14 of the PICS GMP Guide) and other regulatory requirements to comply with Good Manufacturing Practice for Pharmaceuticals. 23-24 October 2024 PIC/S-GMPCRR Face-to-Face ₱6,500.00
Training on Technical Requirements and Regulatory Guidelines for Household Urban Pesticide Products Center for Cosmetics and Household/Urban Hazardous Substances Regulation and Research (CCHUHSRR) The program provides technical assistance to concerned stakeholders on the rules and regulations in the registration of household pesticide products and their active ingredients as well as other regulatory matters applicable for pesticide products. 29-30 October 2024 TR-HUPP Face-to-Face ₱6,500.00
NOVEMBER
Training on 13 Modules of ASEAN Good Manufacturing Practices for Cosmetic Manufacturers and Traders Field Regulatory Operations Office (FROO) The program provides a detailed  discussion on the ASEAN Guidelines  for Cosmetic Good Manufacturing Practice (GMP). 06-07 November 2024 GMP-CMT Face-to-Face ₱6,500.00
Training on Technical Requirements and Regulatory Guidelines for HUHS Products Center for Cosmetics and Household/Urban Hazardous Substances Regulation and Research (CCHUHSRR) The program provides detailed discussions on the technical requirements and procedure for the issuance of Certificate of Product Registration (CPR) for Categories III and IV HUHS Products. 13-14 November 2024 TR-HUHSP Face-to-Face ₱6,500.00
Webinar on Good Distribution and Storage Practice for Medical Products (For Drug Distributors) Field Regulatory Operations Office (FROO) The program will provide an introduction and give an update to the pharmaceutical industry on Good Distribution and Storage Practice as well as their roles in ensuring the safety of pharmaceutical products during transport and storage. 26 November 2024 GDSPMP-DD Online Platform ₱500.00
Webinar on Good Dispensing and Storage Practices for Drug Outlets Field Regulatory Operations Office (FROO) The program will provide an introduction on Good Dispensing and Storage Practices for Drug Outlets and its role in ensuring the safety of pharmaceutical products during storage until dispensed to consumers. 27 November 2024 GDSP-DO Online Platform ₱500.00
Licensing Seminar for Medical Device Establishments Center for Device Regulation and Radiation Health Research (CDRRHR) The Seminar provides the procedural guidelines on the licensing application process and regulatory requirements for Medical Devices Establishments 28 November 2024 LS-MD Online Platform FREE

Please note that the aforementioned schedule is subject to postponement or change due to the unexpected loss of or weak internet connection, sudden power interruption, unavailability of the Resource Speaker/s and other unforeseeable circumstances.

All interested stakeholders shall register through the link and QR Code to be provided for each seminar/training which shall be posted on the FDA website (pornoxxnx.com) and official FDA Facebook Page.  Registration shall be on a first-come-first-served basis.

Registered participants shall wait for the email of the Course Assessment Slip (CAS) to be sent by the FDA Academy. Only the registered participants who received the CAS shall proceed to payment following the instructions provided by the FDA Academy.

Payments made without the required registration and CAS shall automatically be forfeited in favor of the government and shall be non-refundable/non-transferable.

For inquiries and other concerns, please call the FDA Academy at (02) 8877-02-59 or email e-nroll@fda.pornoxxnx.com.