1Industry Standards Development
Collaborate on establishing best practices for literature review, post-market surveillance, and evidence management that the entire industry can benefit from.
Shape the future of evidence management in life sciences
The Evidence Standards Council brings together regulatory experts, medical writers, vigilance engineers, and other evidence professionals to establish industry best practices and influence the tools that shape our daily work.
Your expertise matters. Join peers who are setting the standards that will benefit the entire industry.
1Collaborate on establishing best practices for literature review, post-market surveillance, and evidence management that the entire industry can benefit from.
2Get early access to CiteMed’s Evidence Cloud platform and directly influence features before they’re released. Your feedback shapes tools that streamline evidence workflows across life sciences.
3Earn Evidence Standards Council certification, access exclusive regulatory intelligence, and stay ahead of evolving compliance requirements.
4Connect with vetted professionals through our exclusive job board, gain LinkedIn recognition as a council member, and build your industry network.
For experienced professionals ready to actively shape industry standards
For all experience levels seeking professional development
Establishing validated processes for systematic reviews that satisfy both EU MDR and FDA requirements while reducing time and cost.
Developing guidelines for responsible AI use in evidence management, including validation protocols and audit trail requirements.
Creating standardized workflows that improve communication between regulatory, medical affairs, marketing, and R&D teams.
Streamlining vigilance processes and establishing trending protocols that prevent regulatory issues before they occur.
Collaborative analysis of changing regulations across major markets to keep all members ahead of compliance requirements.
1Influence cost-control initiatives and risk mitigation strategies
2Help develop time-saving tools and advance your career profile
3Shape safety standards and compliance excellence protocols
4Contribute to template development and process standardization
5Establish evidence-based communication guidelines
6Improve literature procurement and access workflows
– Maria L. PMS Engineer, Medical Device Company
– Dr. James R. Regulatory Director, Pharmaceutical Company
– Sarah M.
Medical Writer, Class III Device Manufacturer
Get a demo access to CiteMed and test the functionality that suits your needs
Questions? Email council@citemed.com or schedule a 15-minute call to learn more.