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The Policy and Planning Service – FDA Academy announces the following seminar/training offerings for the 4th Quarter of CY 2022 through online video-conferencing platform, and may include additional program as the need arises:

OCTOBER 2022

Title of Training/Seminar

 

Center/Office Responsible

 

Program

Description

Schedule Course

Code

Registration

 Fee

Webinar on Technical Requirements and Procedure for E-Registration of all Prepackaged and Processed Food Products Center for Food Regulation and Research

(CFRR)

The program provides discussion on how to use the Modified E-Registration Portal version 2 to apply for Certificate of Product Registration for prepackaged, processed food products under the Center for Food Regulation and Research

 

05 October 2022

TR-FP

FREE

Introduction to Pharmaceutical Product Registration Center for Drug Regulation and Research (CDRR) The program aims to provide an introduction and procedural discussion on the regulatory requirements of pharmaceutical products for human use

 

12 October 2022

IPPR

P500.00

Licensing Seminar for Food Establishments CFRR The program provides a procedural discussion on the licensing application process and regulatory requirements for food establishments

 

13

 October 2022

LS-F

FREE

Webinar on Technical Requirements and Regulatory Guidelines for Cosmetic Products Center For Cosmetic 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

 

19 -20 October 2022

TR-RGCP

P1,000.00

Good Distribution and Storage Practice for Drug Products (Drug Distributors) Field Regulatory Operation Office (FROO) The program will provide an introduction to Good Distribution Practice and Storage Practice (GDSP) for Drug Distributors and its role in ensuring the safety of pharmaceutical products during transport or on storage

25 October 2022

GDSP-DD

P500.00

Good Distribution and Storage Practice for Drug Products (Drugstores and Hospital Pharmacies) FROO The program will provide an introduction to Good Distribution Practice and Storage Practice (GDSP) for Drugstores and Hospital Pharmacies and its role in ensuring the safety of pharmaceutical products during transport or on storage

 

27 October 2022

GDSP-DS and HP

P500.00

 

NOVEMBER 2022

Title of Training/Seminar

 

Center Responsible

 

Program Description Schedule Course Code

Registration Fee

Pharmacovigilance 101 CDRR This program aims to provide a discussion on how pharmacovigilance is done and its important role in ensuring the Quality, Safety and Efficacy (QSE) of pharmaceutical products

 

08 November 2022

PV101

P500.00

Licensing Seminar for Drug Establishments CDRR The program provides a procedural discussion on the licensing application process and regulatory requirements for drug establishments

 

10

November 2022

LS-D

FREE

Licensing Seminar for Medical Device Establishments Center for Device Regulation, Radiation Health and Research (CDRRHR) The program provides a procedural discussion on the licensing application process and regulatory requirements for Medical Device establishments

 

15 November 2022

LS-MD

FREE

Licensing Seminar for Household/Urban Hazardous Substances (HUHS) Establishments CCHUHSRR The program provides detailed discussions on the technical requirements and procedure for the issuance of License to Operate to HUHS Establishments.

 

16 November 2022

LS-HUHS

FREE

PIC/S GMP Guide PE009-14: Current Regulatory Requirements 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

 

22-24

November 2022

PIC/S – GMPCRR

P1,500.00

Philippine Mandatory Labelling Guidelines CFRR The program provides discussion on the Philippine Mandatory Labelling Guidelines as stipulated in Administrative Order No. 2014-0030

 

29 November 2022

PMLG

P500.00

 

DECEMBER  2022

Title of Training/Seminar

 

Center Responsible

 

Program Description Schedule Course Code

Registration Fee

Technical Requirements and Regulatory Guidelines for Household/

Urban Hazardous Substances (HUHS) Products

CCHUHSRR The program provides detailed discussion on the technical requirements and procedure for the issuance of Certificate of Product  (CPR) for Categories III and IV of HUHS Products

 

6-7 December 2022

TR-HUHSP

P1,000.00

Introduction to Pharmaceutical Product Registration CDRR The program aims to provide an introduction and procedural discussion on the regulatory requirements of Pharmaceutical Products for Human use

 

 13 December 2022

IPPR

P500.00

Licensing Seminar for Drug Establishments CDRR The program provides a procedural discussion on the licensing application process and regulatory requirements for drug establishments

 

14 December 2022

LS-D

FREE

Payment for the Registration Fee must be settled within the validity period of the assessment slip through bank deposit, and is non-transferable and non-refundable. Absence/Non-appearance during the confirmed training dates automatically forfeits the registration fee.

An assessment slip shall be sent to the registered email of the applicant for the payment of registration fee once the application is approved. The assessment slip has a five (5) working-day validity once sent. Failure to pay within the validity period shall mean automatic cancellation of the application.

After payment, the applicant shall send the scanned copy of receipt and/or assessment slip with bank’s validation within the five (5) working-day validity period to the FDA Academy via email at [email protected], copy furnished the FDA Cashier at [email protected]ph and Accounting Division at [email protected].

Email subject shall follow the format:

Payment for [TRAINING CODE]_[Lastname, Firstname, Middle Initial of enrollee];

Eg: Payment for TR-FP_Dela Cruz, Juan A

Failure to send the scanned copy of receipt and/or assessment slip within the validity period shall automatically forfeit the applicant’s payment and application.

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, or other force majeure.

All interested stakeholders shall register through the link to be provided for each seminar/training which shall be posted at the FDA website (www.fda.gov.ph) and official Facebook page. Registration shall be on first-come-first-served basis.

For inquiries and other concerns, please call the FDA Academy at telephone number (02) 8877-02-59 or email at [email protected].

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