Blog
GSK takes leap into transparency
FierceBiotechIT writer Ryan McBride reports that GlaxoSmithKline (GSK) launched a website that will allow authorized researchers the ability to use clinical study data on certain drugs from the London based pharma company. This launches GSK to the forefront of...
Support the “OK to Ask” campaign
Many doctors already discuss clinical research with patients, but in a recent study, only 21% of patients felt comfortable asking about research to their doctors. The National Health Service, (NHS) is looking for patients and professionals to either ask or talk about...
Pearl Pathways’ own to speak at research conference
The St. Vincent Research and Regulatory Affairs will be hosting the 9th Annual St. Vincent Health Research Symposium on June 12th. Pearl Pathways’ own Ellen Looney, regulatory clinical & quality associate, will be featured, her topic, Good Clinical Practices...
Perspectives between clinical trials sponsors and CROs
Clinical trial sponsors and contract research organizations (CRO) are working together to find a balance between the level of micromanagement and the quality of trials. Outsourcing-Pharma.com’s Zachary Brennan reports that recent studies found that only 41% of...
Medical writing conference hosted by AMWA in June
The American Medical Writers Association (AMWA) will be holding a conference this June covering medical writing topics such as online medical communication, enhanced medical writing, DITA, and more. A variety of speakers throughout the medical writing field will be...