Clinical

Managing a clinical trial is no small feat. Documents must be tracked, client sites monitored, notes and findings to…

The European Union (EU) Clinical Trials Regulation (CTR) harmonizes the processes for assessment and supervision of clinical trials…

Considering switching from a paper trial master file to an electronic one? There’s no better time than now. According to…

Every person who wants to participate in clinical research should have the opportunity to do so…

Managing your Trial Master File (TMF) is a necessary, and often tedious task for most clinical stakeholders—but it doesn’t…

Advances in clinical trial design and technology are significant contributors to medical progress. However, they also hamper clinical operations and…

Change is the lone constant you can depend on. When it comes to scientific discovery, most of that change…

As the outsourcing trend continues to grow, many biopharmaceutical and pharmaceutical companies find themselves needing to partner with CROs (contract…

With declining R&D budgets, increased competition from larger CROs and patent expirations, emerging CROs have evolved from being non-core service…

CRO industry grows as increasingly complex R&D trends demand advanced expertise Among today’s CRO, R&D trends, precision-based medicines and immunotherapies for…