The Society of Clinical Research Associates (SOCRA) 33rd Annual Conference 2024 covers topics such as:
- FDA audit findings and best practices to avoid common pitfalls
- Recent changes to the Common Rule (45 CFR 46)
- How Trial Master File quality can improve site efficiency and effectiveness
- Strategies for quality assurance program development
- Remote monitoring best practices
- The use and benefits of centralized monitoring
- The regulatory and quality parameters of electronic data records
- Adverse event recognition and reporting
- How researchers can renew their emphasis on protections beyond the regulations
- The FDA guidelines for e-consent
- How to successfully implement and use risk based audit programs
- The role and importance of the project manager in clinical research
- Best practices for using e-consent and passing IRB approval
- How tools and strategies that can produce a proactive stance on the responsible conduct of research
- Best practices to avoid common errors in pediatric research
- Techniques to overcome health disparities in research populations
- The process and challenges of expanded access programs
- The regulatory requirements to start and conduct a sponsor-investigator IND trial
- Proven and effective strategies for patient recruitment and retention
- Health Canadas Clinical Trial Compliance Program
- Common issues in multi-national research
- The benefits of self auditing programs
- Best practices for developing market adoption evidence for device studies
- Risk determination in device studies
- Best practices for coding for clinical trials
- Clinical research budget development and negotiation
- Best practice for clinical investigator site source documentation
The Society of Clinical Research Associates (SOCRA) 33rd Annual Conference 2024 brings together clinical research professionals including:
- Research coordinators
- Investigators
- Project managers
- Research associates
- Educators
- Consultants
- Administrators
