Years of preparation allowed Forte to undergo concurrent audits to achieve two ISO certifications within one year. Learn why achieving these certifications confirms Forte’s commitment to delivering high quality, secure solutions for its growing customer community.
With so many electronic data capture systems available, how do you know which EDC is the best fit for your organization? Consider these questions.
Learn how an eRegulatory-CTMS integration can improve workflows and bring additional benefits to your institutional research operations.
Expert webinar presenters answer attendee questions about 21 CFR Part 11 compliance and the validation process for electronic systems.
Take our short survey to share your insights on the use of technology in today’s clinical research industry.
Perfect data doesn’t exist, but better data is still within reach. Learn steps you can take to improve your data collection processes for more trustworthy organizational data.
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.
Three key reasons why vendor-provided hosting and infrastructure could be a more sustainable solution for your clinical research software.
The research industry’s slow adoption of technology has taken on greater urgency as companies like Apple, Alphabet and Amazon step into the world of research, wellness and health care.