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 MoreWhile the COVID-19 pandemic brought many challenges for life science research and development, it accelerated clinical trial innovation to solve long-standing clinical process issues. Read our feature article in pharmaphorum by Caroline Redeker, SVP of Corporate Development at Advanced Clinical, and Moulik Shah, VP of Digital Health at Advanced Clinical, to learn more.
Read MoreThere is a need for seamless data flow throughout the clinical trials ecosystem. Read the PharmaVoice article with Moulik Shah, VP of Digital Health at Advanced Clinical, to learn more.
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 MoreLearn how to manage logistics in a dynamic clinical trial environment.
Read MoreLearn how our team of experts can help you efficiently achieve your safety objectives.
Read MoreJP Miceli, Director of Document Management, talks about what it's like to work in Document Management, and how the great workplace culture at Advanced Clinical is a key benefit of working here.
Read MoreMembers of the Advanced Clinical Biostatistics team candidly discuss what drives them to succeed every day within their function and why they recommend other biostatisticians should join our company.
Read More