EDC eNewsletter September 2008
Applied Clinical Trials' EDC News brings you the latest headlines, features, and resources for everything EDC, from new software to company innovations to IT-related regulations.
invivodata
Register for the Webinar "ePRO Regulatory Environment in Europe" designed to help researchers make decisions about their PRO strategy for clinical programs.
Experience a New Dimension
ClinPhone’s combined EDC-IVR solution provides a single platform for delivering clinical trial logistics and data management. Contact us today: [email protected]
eClinical Forum Autumn Meeting
October 6–8, 2008
Location | Brussels, Belgium
eDC SIG Meeting
October 30, 2008
Location | Takeda, London
Structured Product Labeling (SPL) Preparing for FDA Electronic Registration and Drug Listing
October 29–30, 2008
Location | Philadelphia, PA
Lex Jansen
joins Octagon as senior consultant of clinical data strategies.
Steve Shevel
has been added as a new associate to the Waife & Associates' staff.
Robert Barr
joins Nextrials as the new chief technology officer.
Applied Clinical Trials will release its EDC & Information Technology supplement with the October issue. Bookmark and check back!
Octagon Research Solutions has added an EDC blog and discussion forum to its Web site.
ClinPage has amassed its list of eClinical Suite providers.
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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.
FDA-Approved Gene Therapy Beqvez Shows Sustained Efficacy, Safety in Long-Term Hemophilia B Trial
April 17th 2025Beqvez (fidanacogene elaparvovec), an FDA-approved one-time gene therapy for hemophilia B, demonstrated sustained factor IX expression, low bleeding rates, and a favorable safety profile over long-term follow-up.
