Navigating New Terrain: The Impact of Evolving EU Regulations on Regulatory Affairs
Presentation Materials Don't miss Part 2 in the series Joint Advice on FDA/EMA Compliance…
Danielle Pillsbury2024年8月20日
Using Quantitative Systems Pharmacology (QSP) Modeling for Oncology Dose Optimization
The FDA’s Project Optimus initiative aims to reform dose optimization and selection for oncology therapies…
Danielle Pillsbury2024年8月19日
Mastering Value Storytelling in Healthcare: Leveraging Digital Tools to Meet Stakeholders’ Expectations
Everyone loves a good story. Stories are more likely to move and engage people than…
Danielle Pillsbury2024年8月14日
Summarize This! GPT Prompts for Regulatory Writers
With the advent of GPTs, regulatory writers face an opportunity and a challenge. The opportunity?…
Simona Colucci2024年8月8日
Sponsored Webcast: Best Practices for Simultaneous Submissions to EMA/FDA
Sponsor companies are now expected to submit globally as quickly as possible. Successful achievement of…
Danielle Pillsbury2024年7月25日
Hosted Phoenix for High Performance PK/PD
PK/PD解析と薬物動態モデリングにおいて、どのように効率を最大化しますか？Well-trained scientists, reproducible workflows,…
Danielle Pillsbury2024年7月8日
Technologies for the analysis and utilization of vast amounts of data in drug discovery research [Japan Webinar]
このウェビナーは日本語のみでの開催となります。Certara introduced D360, a drug discovery research…
Danielle Pillsbury2024年7月3日
How AI-powered writing software can bring a benefit in Japan [Japan Webinar]
このウェビナーは日本語のみでの開催となります。Medical writing is a critical part of…
Danielle Pillsbury2024年6月27日
Catalyzing DMTA Information into Insights
Drug discovery is a data-driven research process that requires accurate data capture, ample and reliable…
Danielle Pillsbury2024年6月27日
