More Than Your Average Training and Consultancy
In line with the implementation of Republic Act 11032, otherwise known as the “Ease of Doing Business and Efficient Government Service Delivery Act of 2018”, the PDEA Compliance Service has revised and simplified the procedure and requirements for the application of S2 License, S License, P License and Accreditation, effective November 1, 2021. To view
For ALL OPMS and CRS Accounts: Please be informed that before registering on the Online Permitting and Monitoring System (OPMS), one must first register on the Company Registration System (CRS). For those who have already an OPMS account, please be informed that your account will be limited on functionalities until you link your registered CRS
***Draft for Comments || Revised Guidelines on Good Manufacturing Practice (GMP) Clearance for Foreign Drug Manufacturers *** All comments can be sent at oddgfroo@fda.gov.ph. Deadline of submission of comments shall be by 21 November 2021. I. RATIONALE AND BACKGROUND Consistent with State policy under Section 3 of RA 9711 “(a) protect and promote the right
[NEW WEBINAR] Leadership in the Era of Volatile, Uncertain, Complex and Ambiguous— For Middle and those who are expected to be Leaders — Lecturer:Prof. Yoshio OnoProfessor, Faculty of Economics, Shiga University Monday 13 Dec. 202112:30PM – 3:30PM (Manila) [LECTURE CONTENT]<Lecture>1. Clarification of leadership and management as well as significance/concept of organization2. Manager’s view of humanity underlying 1.
The Food and Drug Administration (FDA) encourages healthcare providers, consumers, and patients to report suspected adverse reactions following the use/administration of drugs and vaccines.Here are the ways on how to report adverse reactions to drugs and vaccines: • https://www.fda.gov.ph/pharmacovigilance/ • https://primaryreporting.who-umc.org/PH For more information and inquiries, kindly contact the Pharmacovigilance Section at 8809-5596 or email
#ADVISORY: In view of the approved recommendation by the IATF to place Metro Manila under Enhanced Community Quarantine on August 6 to 20, 2021, FACE- TO- FACE TRANSACTIONS shall be suspended at the FPA Central Office and affected Regional Field Units during the period. The use of our online scheduler for booking face-to-face appointments in
Nais maging licensed fertilizer handler? Sa pangalawang episode ng FPA Webinar Series, ating tatalakayin ang proseso at requirements sa pagkuha ng License to Operate (LTO) bilang Manufacturer, Processor, Formulator, Bulk Blender, Bulk Handler, Importer, Importer End-User, Institutional User, Indentor, Exporter, Repacker, Area Distributor, and National Distributor. Lubos naming inaanyayahan ang mga Farmer’s Organizations at Associations
***FDA Advisory No.2021-2491*** The Center for Drug Regulation and Research (CDRR) of the Food and Drug Administration (FDA) will be conducting an inventory and processing of the pending applications for registration of drug products for human use. As such, the period 15 November 2021 to 15 January 2022 is hereby declared as an Application Holiday.
[NEW WEBINAR] <Kaizen Marathon Series> Innovative Cost Reduction Approach from Japan – MFCA ~ Challenge to Low Cost Kaizen ~Lecturer: Mr. Tatsuhiko TomiiManaging Director, One Asia Consulting Co., Ltd. [LECTURE CONTENT] 1. Overview of MFCA (Material Flow Cost Accounting/ Analysis) 2. Realization of both cost reduction & environmental burden 3. Practice case of MFCA in Japan
Mongolia-AOTS will organize a WNF program titled “Developing new Initiatives using Lean Business Model.” The three-day webinar series, starting October 20, will explain the following. • To introduce Lean methodology to eliminate any form of waste in new initiatives (ventures) and be efficient with resources; • To provide a clear roadmap in developing Lean canvas;•