On Tuesday, February 16th, learn the latest information on Decree 650 and changes in device guidance, regulations, and in-China clinical trials in a webinar presented by Brandwood Biomedical Director of China Operations, Steven Wen. Click here for your free...
Pearl Pathways’ own COO and Co-Founder, Gretchen Bowker will be holding a webinar on FDA regulatory requirements for the manufacturing and commercialization of dietary supplements via ComplianceOnline. A few of the topics include a review of FDA regulations in the...
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...
On August 8, 2013, Gretchen Bowker, co-founder and COO of Pearl Pathways, will host a webinar on ComplianceOnline.com reviewing the similarities and differences in the regulatory paths and requirements for drugs, biologics and medical devices. It will discuss the...
Do you work at a site as a clinical research coordinator and need a deeper dive into Good Clinical Practices (GCPs)? Are you a sponsor who has responsibility for oversight and training of site personnel? On July 26, 2013, Pearl Pathways’ own Ellen Looney will lead a...
