BioClinica Inks Seven New Trident IWR Deals in First Quarter 2011
BioClinica
announced that Trident IWR (interactive web response) has been
selected
by seven new clients in the first quarter of 2011 to help build and deploy complex trials efficiently without the need for programming.
Trident IWR provides clinical operations personnel a way to directly set up, monitor, and maintain randomization and supplies for their clinical trials, in a less costly manner and in a fraction of the time than previous alternatives. Trident IWR does not require programming for each new clinical trial and it configures both web and voice at the same time..
In December of 2010, GlaxoSmithKline signed an
agreement
with BioClinica to standardize on the Trident IWR system, selecting the technology as a way to manage their global trials across Phase I-IV clinical trials.
“Since we launched Trident IWR in October 2010, BioClinica has received incredible industry-wide response,” said Mark Weinstein, CEO of BioClinica. “With seven companies making the decision to standardize their complex trials with Trident IWR in just the first quarter of 2011 alone, we are happy to confirm that our best-in-class solution is successfully providing the efficiencies, cost savings and overall support needed by today’s top pharmaceutical companies.”
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.
