There are many standards available for defining safety and efficacy clinical trials data across industry, academia and government. Some are obvious, such as CDISC, but some are less well known. Some are required, others are highly recommended. Most provide existing materials that can jumpstart research, save time and money and provide numerous other benefits. This webinar:
- Explores the definitions of "standards"
- Reviews a wide range of data and process standards relevant to clinical research, including CDISC, initiatives at NIH, ISO standards, electronic health record initiatives and process improvement standards
- Discusses the wider importance of using standards
Learning Outcomes:
- Define the term “standards” in different contexts
- Identify standards that are useful or required for various types of research
- Select external standards that can benefit internal standards development and implementation
This webinar will benefit:
- Heads and colleagues in:
- Standards management
- Process improvement
- Clinical data management
- EDC design and programming
- CRF design
- Database programming
- Biostatistics
- Clinical science/study management
- Clinical Operations
- People who are already familiar with the research landscape as well as those who are new to it
Panelist:
- Kit Howard, Director of Education, CDISC