The Development Regulatory Affairs for Oncology Medicinal Products 2015 is a webinar that covers topics such as:
- Regulatory strategy in oncology
- Covered in the Session:
- Small patients populations
- One pivotal study
- Faster approval pathways
- Scientific advice
The Development Regulatory Affairs for Oncology Medicinal Products 2015 is intended for:
- Project Managers
- Senior management
- CRAs and CRCs
- Medical writers
- Investigators
- QA / Compliance personnel
- QA / QC Auditors and Staff
- Clinical Research Scientists
- Consultants
