by Nick | May 12, 2023 | Clinical Research, oncology
For all clinical trials, it is crucial that the potential benefits of a medicinal product are determined, while monitoring any potential side effects. However, for early-phase oncology trials, the extensive monitoring of adverse events (AEs) is essential, considering... 
by Nick | Apr 18, 2023 | Clinical Research, Pharmacovigilance
Welcome to the fascinating yet complex world of Pharmacovigilance (PV)! This field stands as an indispensable pillar in drug safety, ensuring the well-being of millions around the globe. However, the path is far from smooth; it’s full of unique challenges and... 
by Nick | Mar 21, 2023 | Clinical Research
Clinical research is an integral aspect of the healthcare industry. It plays a vital role in developing and approving new treatments and drugs. Clinical research organizations (CROs) specialize in providing services to support clinical research activities. One of the... 
by Kamile Gruduls | Mar 9, 2023 | Announcement, Clinical Research, Medical Information, Pharmacovigilance, Regulatory Affairs
Recently, we had the chance to reflect on our last 10 years of operations and were astonished by the unprecedented growth facts: The Clinical Research department grew 8 times the size it was back in 2013. Regulatory Affairs services became available to 32 new... 
by Nick | Mar 7, 2023 | Clinical Research, Pharmacovigilance, Regulatory Affairs
The role of Contract Research Organizations (CROs) in supporting mergers and acquisitions (M&As) is not a new concept, as CROs have been providing services in this area for several years. However, the demand for these services may have increased in recent years... 
by Nick | Feb 28, 2023 | Clinical Research
Designing effective early-phase oncology trials is a complex and challenging task, requiring careful consideration of various factors, including patient selection, dosing, safety monitoring, and endpoint selection. In addition, developing targeted therapies has... 
