How to support employee mental health and create a happy and productive team. PHARMExcel explores new well-being initiatives for office and remote workers.
The process of taking a pharmaceutical drug through its drug discovery pathway can be challenging, time consuming, and expensive. It’s why more and more leading biotech and pharma companies choose to outsource clinical research work to contract research organisations (CROs) instead.
This month PHARMExcel reaches yet another milestone as it celebrates 13 years of successful business.
This programme, (supported by CEPI funding), will provide the infrastructure to help design and select the lead antigen through proof-of-concept preclinical studies, progressing to initial clinical development through Phase I/II studies. DIOSynVax aim to establish clinical proof of concept for a novel vaccine candidate with the potential to provide broad protection against Sarbecovirus, Merbecovirus, Embecovirus and Nobecovirus.
Following its reputation of excellence in delivering investigator-led studies, PHARMExcel was selected to manage the Covid-19 vaccine booster study.
The new EU clinical trial regulation (CTR) is set to revolutionise clinical trial processes across Europe impacting all European Member states and organisations wanting to run clinical trials across these regions. How can organisations prepare for the change and set themselves up successfully with a new CTR programme?
Meet Martha Nabunjo Clinical Research Associate I (Clinical Monitor) “I’ve worked at PHARMExcel almost a year now and I must say in this short space of time, I am very lucky to have had the opportunity to work on some very high-profile studies. What I enjoy most about my role here is that every day…