[2025 Continuing Education] - Announcement of Implementation of Continuing Education for Regular Members of Technical Qualification Certificates
- 등록일2025.01.02
- 조회수2,659
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 | |
| Apr 11, 2025 | 4hr | Quality Risk Management Practice | |
| May 29, 2025 | 4hr | Pharmaceutical Facility Standards & Application | |
| Aug 20, 2025 | 4hr | Pharmaceutical Plant QA Operation Practice | |
| Sep 30, 2025 | 4hr | Env. Monitoring Location Selection RA & CCS | |
| Dec 12, 2025 | 4hr | GMP Inspection Practice |
- 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)
- 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.
- 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 |
| 90 days | Understanding Pharmaceutical Process (Package) | 26,370 |
[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.
ENG
KOR
PTF
ICPI WEEK