In this insight brief, our experts explore the fundamentals of feasibility, the necessity of broadening approaches, the best way to leverage technologies and processes, and how a multichannel combination of techniques can deliver more actionable insights from feasibility assessments.
Read MoreIn this insight brief, our experts discuss proven recruiting techniques that sponsor companies can apply to attract more–and better qualified–candidates in a highly competitive market.
Read MoreFor years, the promise of therapeutic cancer vaccines has intrigued researchers working in the oncology space. Read our feature article in pharmaphourm by Christopher Oelkrug, Director of Business Development, to learn about the advancements and innovations made in therapeutic cancer vaccine research.
Read MoreRead our Applied Clinical Trials article by Kimberly Wanick, VP of Compliance and Quality, to learn about the cultural changes that need to be made to allow for leaders to place more of an emphasis on employee wellbeing, which can ultimately help reduce disruptions in clinical trials.
Read MoreIn this webcast, learn how organizations can work with their partners to optimize feasibility assessments, mitigate risks and improve results.
Read MoreIn this webinar, learn about proven recruiting techniques that you can apply today to attract more candidates and convince them to accept offers quickly – while creating an engaging employee experience for talent.
Read MoreLearn how our Medical Writing team developed a partnership with a mid-sized, biotech company after authoring support for one Clinical Study Protocol.
Read MoreLearn how we streamlined quality management using the Veeva Vault Quality Suite to improve the speed and efficiency of our clinical operations.
Read MoreAuditing is an essential element and key function within clinical trials, helping companies ensure patient and product safety, avoid gaps in compliance and prepare for regulatory inspections. In this white paper, we examine the key steps in audit performance – planning, preparation, conduct, reporting, follow-up, and closure – outlining the differences and similarities in process and scope of review between GCP and GMP-focused audits.
Read MoreDespite the increase in eTMF utilization, Health Authority attention and sponsor awareness, TMF Quality continues to be an issue for many organizations. Issues in TMF Quality are driven by many factors, including the complexity of today’s trial protocols, frequent change in outsourcing models, and the use of new eClinical systems, to name a few. In this white paper, we will discuss how it is possible to attain TMF Quality sufficient to withstand health authority inspection by thoughtful and deliberate management of four key TMF cornerstones.
Read MoreFind out how we can better predict the outcomes of your trial with our customized approach for meeting your study's protocol, country and site feasibility goals.
Read MoreLearn about how our commitment to diversity, health equity and inclusion helps us provide a better clinical experience to all those who are touched by clinical research.
Read MoreTracy Turner, Director of Project Management, talks about her career journey in the clinical industry and how it led her to join the Advanced Clinical team.
Read MoreSatya Dandugula, Senior Manager of Statistical Programming, discusses how his career in clinical research led him to working at Advanced Clinical. He emphasizes the importance of personal touch in the recruitment process, which he found in our personalized recruitment approach.
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