How to Transition from Paper to Electronic Records in a Regulatory Environment 2015 is a webinar that covers topics such as:
- Records data map
- Records policy and procedures
- Converting paper documents into a useful electronic format
- Incorporating paper records into a eCTD
- Indexing and organizing scanned records and integrating them
- Scanning costs and resources
- Big data – implications to the drug business
- Long term record storage and retrieval
How to Transition from Paper to Electronic Records in a Regulatory Environment 2015 is intended for personnel from pharmaceutical and clinical trial companies, involved in:
- Scientists
- Research & Development
- Clinical Research (project managers, investigators, study coordinators, operations, QA and document managers)
- Regulatory Affairs
- Information Technology
- Legal
- Documentation
- Validation
