We invite you to join us at the second session of Indiana Medical Device Manufacturers Council (IMDMC)’s annual Regulatory 101 course on August 19, 2014. This is a popular event designed for staff who are new to the FDA regulatory world or those who just need a...
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...
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...
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...
Cassandra Leger from bioresearchonline.com covered recent development regarding the National Institute of Health’s (NIH) plans to create a program to expedite research designed to treat brain disorders. The NIH is planning on turning their new biospecimens...
Plan on joining us at the Indiana Medical Device Manufacturers Council (IMDMC) event entitled “Regulatory 101” on May 15, 2014. Gretchen Bowker, COO of Pearl Pathways will be speaking at the event at the Montage Banquet Hall in Indianapolis, Indiana. This is a full...
