| Event | Regulatory Affairs Part I: The IND Phase | mkeller28 | 0 | 2 years 12 weeks ago |
| Event | Overview of Drug Development in Japan | mkeller28 | 0 | 2 years 12 weeks ago |
| Event | Regulatory Affairs for Biologics | mkeller28 | 0 | 2 years 12 weeks ago |
| Event | Regulatory Affairs Part I: The IND Phase | mkeller28 | 0 | 2 years 12 weeks ago |
| Event | Regulatory Affairs Part I: The IND Phase | mkeller28 | 0 | 2 years 12 weeks ago |
| Event | Overview of Drug Development in Japan | mkeller28 | 0 | 2 years 12 weeks ago |
| Event | Regulatory Affairs for Biologics | mkeller28 | 0 | 2 years 12 weeks ago |
| Event | Regulatory Affairs Part II: The NDA Phase | mkeller28 | 0 | 2 years 12 weeks ago |
| Event | Leadership Experience | mkeller28 | 0 | 2 years 12 weeks ago |
| Event | 11th Conference on European Electronic Document Management | mkeller28 | 0 | 2 years 13 weeks ago |
| Event | Workshop on Statistical Methodology in Clinical R&D | mkeller28 | 0 | 2 years 13 weeks ago |
| Event | DIA European Regulatory Affairs Forum 2010 | mkeller28 | 0 | 2 years 13 weeks ago |
| Event | The 1st DIA Cardiac Safety Workshop in Japan | mkeller28 | 0 | 2 years 13 weeks ago |
| Event | 3rd Annual Regulatory Conference on Global Regulatory Challenges: Quest for Optimization | mkeller28 | 0 | 2 years 13 weeks ago |
| Event | DIA and FDA Office of Women’s Health (OWH): Strategies for Ensuring Representation of Patient Demographics in Clinical Research for Regulatory Review | mkeller28 | 0 | 2 years 13 weeks ago |
| Event | Innovation Forum | mkeller28 | 0 | 2 years 15 weeks ago |
| Event | CTD Dossier Requirements Focus on EU Module 1 and Quality Module 4 | mkeller28 | 0 | 2 years 15 weeks ago |
| Event | 46th DIA Annual Meeting | mkeller28 | 0 | 2 years 15 weeks ago |
| Event | 22nd Annual EuroMeeting | mkeller28 | 0 | 2 years 15 weeks ago |
| Event | CTD Dossier Requirements Focus on EU Module 1 and Quality Module 3 | mkeller28 | 0 | 2 years 15 weeks ago |
