Blog
SCRS webinar “Preparing for an FDA Audit,” presented by Gretchen Bowker, COO on December 16, 2014
We are pleased to announce that Pearl Pathway’s own Gretchen Bowker will be presenting a webinar on preparing for an FDA audit in December for the Society of Clinical Research Sites. Clinical research sites for biopharma and medical device companies are seeing a...
ACRES launches global interface for clinical research
The Alliance for Clinical Research Excellence and Safety (ACRES), a growing global network created to improve the safety, quality, and efficiency of clinical research, has announced their initiative to construct an open information platform supporting clinical...
Implementing QbD methods for clinical research
An interesting article by Zachary Brennan on outsourcing-pharma.com highlights the current status in the adoption of quality by design (QbD) methods for clinical research. According to the results of a survey presented at this year’s Avoca Quality Consortium Summit,...
Physicians push to increase hispanic enrollment in clinical trials
Elizabeth Allen of The Cancer Therapy & Research Center (CTRC) at The University of Texas Health Science Center posted a news release emphasizing the importance of clinical trial enrollment among the Hispanic population, which is currently an astoundingly low...
FDA poised to increase China inspections
Gareth Mcdonald from in-pharmatechnologist.com shared his views on the impact of FDA committing a forecasted $5 million of its newly approved budget to visit Chinese drug plants. The reason for the increase attention in China is that FDA wants to focus on facilities...