Popsi Cube provides its pharmaceutical company sponsors with expertise in both clinical trial management and in IT services. This dual competency allows us to monitor phase I to IV clinical trials and develop tools which are specific to the needs ofour clients.
In addition to providing the full range of early- to late-stage clinical development services for the world's biopharmaceutical industry, Popsi Cube is offering specific tailor made solutions and numerous applications in such fields as randomization, data capture, data management, or eCTMS compliant with EMEA and FDA regulations and quality guidelines to facilitate the clinical development process. In particular, we have developed an array of data capture solutions, from Digital Pen and Paper data capture, to eCRF, IVRS/IWRS and PDA/tablet PCs, allowing us to offer the technology that best matches the specificities of the study protocol.
To be able to best support the growing demands of our North American sponsors, Popsi Cube has decided to open a new affiliate in the US. The new company, Popsi Cube, Inc., is based in Philadelphia, PA. Our new location will allow us to support our growth objectives by establishing close relationships with our customers and by providing them with local, experienced management support for their projects.
The Company’s North American expansion is funded by a grant from COFACE on behalf of the French state, providing further recognition of the interest of our solutions and potential in North America.
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.