We are pleased to announce our recent updates to the Pearl IRB website. In the Resources section, you will find new and revised forms to serve you in the IRB submission process. Some of these changes include: Updated submission guide and policies, which we suggest all...
inVentiv Clinical Trial Recruitment Solutions (iCTRS) shared good news in a recent article posted on dddmag.com regarding perceptions of potential clinical trial participants.. The Center for Information and Study on Clinical Research Participation (CISCRP) conducted...
Among the many obstacles drug companies face in bringing a product to market, recruiting clinical trial volunteers has become increasingly difficult, according to a recent article on www.washingtonpost.com by Lenny Bernstein. Bernstein states that more than 10% of...
FDA has issued final guidance concerning the transfer of clinical studies between IRBs. According to Zachary Brennan on www.outsourcing-pharma.com, FDA says the transfer process “should be accomplished in a way that assures continuous IRB oversight with no lapse in...
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...
