[2025 Continuing Education] - Announcement of Implementation of Continuing Education for Regular Members of Technical Qualification Certificates

Date2025.01.02
Hit2,687

Greetings.

This is the Pharmaceutical Technology Foundation / GMP Association.

This is an announcement regarding the Refresher Training schedule for regular members who hold GMP Technology or Validation Technology certifications.

Certified members are required to attend training once a year to maintain their certification benefits.

Eligible Participants: All certification holders from 2010 to 2024
Recognition Period: January 1, 2025 – December 31, 2025

Please select and apply for one of the following education options at your discretion.

1. Regular Seminar Refresher Training Schedule

※ A 20% discount is provided for Regular Seminars.

1.1 Schedule

Date	Hours	Topic	Cost (KRW)
Feb 18–19, 2025	8hr	Document Management & Data Integrity Operation	~~198,000~~ → 158,400
Apr 11, 2025	4hr	Quality Risk Management Practice	~~99,000~~ → 79,200
May 29, 2025	4hr	Pharmaceutical Facility Standards & Application	~~99,000~~ → 79,200
Aug 20, 2025	4hr	Pharmaceutical Plant QA Operation Practice	~~99,000~~ → 79,200
Sep 30, 2025	4hr	Env. Monitoring Location Selection RA & CCS	~~99,000~~ → 79,200
Dec 12, 2025	4hr	GMP Inspection Practice	~~99,000~~ → 79,200

1.2 How to Apply

Log in to Website → [GMP Education] → [Apply for Regular Seminar] → Select the relevant [Refresher Training Course].
In the participant information section of the application, please mark your name with 'G' or 'V'.
Ex) Hong Gildong/G (GMP Technology holder ⇒ G, Validation Technology holder ⇒ V)

1.3 Payment Method

Bank Transfer: Shinhan Bank / 100-033-734158 / Pharmaceutical Technology Foundation
* Please deposit under "Company Name-Attendee Name"
Website Payment: Credit card or real-time account transfer available.

1.4 Proof of Payment

Tax invoice, cash receipt, card payment receipt, transaction statement, etc.
Tax invoices will be issued in bulk on the training date after deposit confirmation. (Please contact the secretariat if you need it issued in advance.)

2. E-Learning Basic Course Refresher Training Guide

2.1 Course List

Category	Period	Course Name	Cost (KRW)
Validation 2	90 days	CSV Course (Package)	20,790
	90 days	Process Validation (Package)	14,850
	60 days	Analytical Method Validation (Package)	14,850
	90 days	Qualification (Package)	14,850
Quality Manual	90 days	QS_Quality System (Package)	23,760
	60 days	6 Systems of Quality Manual (Package)	8,250
	60 days	Lab Control System (Package)	14,850
GMP Course	60 days	Facilities & Utilities (KFDA Standards) (Package)	11,000
GMP Course	90 days	Understanding Pharmaceutical Process (Package)	26,370

2.2 How to Apply

[Log in to Website] → [GMP Education] → [E-Learning Basic Course] → Select your desired course.

2.3 Note

After completing the E-Learning Basic Course, please leave a message via "1:1 Inquiry" on the website or send an email with your completion details. We will process it as recognized refresher training after verification.
(Period: Within Jan 2025 ~ Dec 2025)

Thank you.

댓글목록

등록된 댓글이 없습니다.

List