The IR Technical Education Institute is hosting an online public seminar focusing on the 'overall consistency' essential for creating pharmaceutical approval application documents (CTD-Q), teaching the '7 perspectives' and efficient procedures. The three requirements for high-quality CTD-Q are regulatory compliance, scientific accuracy, and overall consistency. This seminar aims to organize practical perspectives to connect known knowledge into a cohesive whole for consistent CTD-Q creation. The live session is scheduled for July 15, 2026, with archive access available from July 17 to July 31. The fee is 29,700 yen per person.
FACT BOX
- Source: PR TIMES
- Category: event_announcement
- Dates in source: 2026/7/15 / 2026/7/17