Intralinks For Clinical Operations
Successfully manage your clinical development programs.
Our security and governance capabilities, including ISO 207001 certification, FDA 21 CFR Part 11 validation and HIPAA compliance, were designed to protect high-value information for the most-regulated industries.
Drug companies are under pressure to accelerate clinical development while reducing costs and maintaining compliance with a web of regulations and agency guidelines. Promising compounds need to be brought to market quickly or terminated early, and sponsors are becoming increasingly reliant on strategic partners and key external contributors.
Intralinks is used by over 60,000 investigator sites and supports over 2,100 active clinical trials. Our security and governance capabilities, including ISO 207001 certification, FDA 21 CFR Part 11 validation and HIPAA compliance, were designed to protect high-value information for the most-regulated industries.
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Data Monitoring Committees (Independent Safety Review Boards)
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Safety Document Distribution (SUSAR Notification)
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Study Start-Up and Site Activation
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​Remote Monitoring and Electronic Investigator Site Files