Forte’s director of product management attended the SCDM Annual Conference earlier this month, and took the time to reflect on the growth of the clinical data management domain.
With so many electronic data capture systems available, how do you know which EDC is the best fit for your organization? Consider these questions.
Expert webinar presenters answer attendee questions about 21 CFR Part 11 compliance and the validation process for electronic systems.
Watch this webinar to hear our expert presenters provide an overview of 21 CFR Part 11 and discuss the roles both organizations and vendors play during the validation process.
Forte’s development approach is to not only navigate industry regulations, but to strategize how to best serve and assist our community. Learn Forte’s philosophy towards developing 21 CFR Part 11 compliant systems.
Use these five fundamental elements of clinical data management to implement quality data practices across your research organization.
Expert webinar presenters answer attendee questions about data quality best practices and steps to grow their careers in data management.
Shopping for a validated EDC system can seem like a daunting task. Learn five steps that make the process less confusing.
A disaster preparedness plan is key to ensuring unforeseen hazards won’t impact your trial. Make sure your EDC system is included in your plan.