IntraLinks
, a provider of critical information exchange solutions,
announced a partnership
with
SAFE-BioPharma
, the non-profit association that created and manages the SAFE-BioPharma® digital identity and signature standard for the pharmaceutical and healthcare industries. IntraLinks users will now be able to use the SAFE-BioPharma digital identity for signing documents. They can increase clinical trial efficiency by signing paperwork with a SAFE credential that provides additional security and speed, eliminating printing of hard copy casebooks and other documents.
Users will have the opportunity to upload and use their SAFE-BioPharma digital identities on the IntraLinks® platform, ensuring that their credentials are available anywhere via the Web. IntraLinks is also enabling documents signed with SAFE-BioPharma signatures to be stored and shared on its existing platform.
“Incorporating SAFE-BioPharma’s digital identity and signature standard into IntraLinks’ platform is very significant for our clients and the community who rely on IntraLinks to manage their clinical trial communication and document exchange,” said Alison Shurell, VP, life sciences product marketing, IntraLinks. “In addition to already being able to securely upload, receive, review and distribute documents on IntraLinks, sponsors, CROs and investigators will soon be able to eliminate the need to print out or physically store the numerous documents that require signatures during a clinical trial."
In addition to incorporating the digital signature into its platform, IntraLinks has joined the SAFE-BioPharma vendor partner community.
Improving Relationships and Diversifying the Site Selection Process
April 17th 2025In this episode of the Applied Clinical Trials Podcast, Liz Beatty, co-founder and chief strategy officer, Inato, discusses a number of topics around site engagement including community-based sites, the role of technology in improving site/sponsor relationships, how increased operational costs are impacting the industry, and more.
Behind the Buzz: Why Clinical Research Leaders Flock to SCOPE Summit
February 7th 2025In this episode, we meet with Micah Lieberman, Executive Conference Director for SCOPE Summit (Summit for Clinical Ops Executives) at Cambridge Innovation Institute. We will dive deep into the critical role of collaboration within the clinical research ecosystem. How do we bring together diverse stakeholders—sponsors, CROs, clinical trial tech innovators, suppliers, patients, sites, advocacy organizations, investors, and non-profits—to share best practices in trial design, program planning, innovation, and clinical operations? We’ll explore why it’s vital for thought leaders to step beyond their own organizations and learn from others, exchanging ideas that drive advancements in clinical research. Additionally, we’ll discuss the pivotal role of scientific conferences like SCOPE Summit in fostering these essential connections and collaborations, helping shape the future of clinical trials. Join us as we uncover how collective wisdom and cross-industry partnerships are transforming the landscape of clinical research.