Advarra Brochures
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Streamline Your Regulatory Process
1/18/2022
The Advarra eRegulatory Management System (Advarra eReg) provides integrated protocol, staff, and institution documentation to streamline regulatory process and enhance compliance.
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Study Startup Support
1/18/2022
As a key element of study startup, IRB review can have a substantial impact on meeting critical study milestones. Advarra provides flexible solutions to help accelerate the initial IRB review process and make it more efficient.
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Quality Center Of Excellence
12/17/2021
As value chains extend around the globe, regulations evolve, and organizations feel the pressure to accelerate the speed at which they bring innovation to market; the need to maintain and optimize quality management systems has become more critical.
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SiteIQ
12/2/2021
Accelerate study startup, gain valuable insights, and increase visibility with customizable site performance metrics.
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Optimize Your Research Administration, Compliance, And Operations
12/2/2021
Develop, implement, and uphold research compliance and administrative practices in alignment with federal regulations, state and local law, and industry best practices.
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Custom eLearning Services
12/2/2021
In this brochure, learn how Advarra’s eLearning creates consistent and engaging training, scalable across your whole organization.
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Pandemic Response Assessment
8/9/2021
In the face of the COVID-19 pandemic, biopharmaceutical companies had to react quickly to develop and implement what were frequently large scale crisis response initiatives. Read how now is the time to assess the changes that were implemented and refine business continuity plans to ensure regulatory compliance, patient safety, and organizational preparedness now and into the future.
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Virtual Investigator Meetings By Advarra
6/10/2021
Advarra’s unmatched, comprehensive suite of training services helps sponsors and CROs ensure efficient and compliant training at their sites. Powered by Longboat, Advarra can create custom protocol training and deliver training to site staff via a sleek, intuitive 21 CFR Part 11 compliant platform.
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Advarra Regulatory Consulting
6/10/2021
Our regulatory consultants take action and move your research forward. If you’re looking for help in the development of innovative life science and digital health products, then Advarra® is the answer.
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Get Help With Institutional Biosafety Committee Reviews
3/30/2021
Crafting an IBC review involves the deliberate transfer of engineered genetic materials to human research subjects. Read Advarra's latest brochure on how they can assist with your next IBC review.