The 7th Clinical Regulatory Medical Writing Forum 2020 covers topics such as:
- How your peers manage data sharing, redactions and the anonymization of patient data
- The new EU clinical trials regulation, the challenges of preparing lay summaries and how to stay ahead of the curve
- The challenges of preparing pediatric documentation
- How to prepare a risk management plan and safety documents for the different regional regulatory authorities
- Which tools and technologies can help expedite the medical writing process
The 7th Clinical Regulatory Medical Writing Forum 2020 brings together senior attendees from pharmaceutical and biotechnology companies with responsibilities in:
- Regulatory Submissions/Documentation
- Medical/Regulatory/Scientific/Clinical/Technical Writing
- Clinical Data Transparency
- Clinical Trial Disclosure
- Clinical Operations/Development
- Clinical Documentation/Publication
- Medical/Scientific Communications
- Clinical Research
- Medical Affairs
- Medical Publication
- Global Medical Publishing
- Regulatory Affairs/Operations
As well as:
- Clinical Research Organizations
- Medical Writing Service Providers and Consultants
- Information Management Consultants
- Document Application Suppliers
- Component Authoring Software Suppliers
- Research Informatics
- ECTD Suppliers
- Bibliographic Software Suppliers
- Structured Content Software Suppliers
- Regulatory Submissions Providers