Bobbi Drais Promoted to Vice President, Regulatory Affairs for HEALTHPOINT, Ltd.
Since joining Healthpoint in 2003, Ms. Drais has achieved landmark regulatory success for DFB and Healthpoint. Ms. Drais initially established the regulatory department for Healthpoint. She and her team secured new drug approval (NDA) and marketing authorization approval (MAA) for ATRALIN(TM) (tretinoin) Gel in the US and
“With Bobbi at the helm of all regulatory functions, I have great confidence that Healthpoint can seamlessly continue along its trajectory of success,” said
Prior to joining the DFB family of companies, Ms. Drais was Regulatory Affairs Manager for Galderma Laboratories, LP, Carrington Laboratories, Inc. and Smith & Nephew, Inc.
Ms. Drais graduated from
Since 1992, HEALTHPOINT has been dedicated to innovative technologies for the prevention and treatment of acute, chronic and burn-related wounds. The company is presently focused on the research and development of novel biologics and pharmaceuticals intended to improve clinical and quality of life outcomes. Currently marketed products include: Collagenase SANTYL(R) Ointment, OASIS(R) Wound Matrix, HYDROFERA BLUE(R) Bacteriostatic Wound Dressings, and SURGICEPT(R) Waterless Surgical Hand Antiseptic. HEALTHPOINT is also committed to advancing the care and treatment of wounds through support of industry leading continuing education from THE WOUND INSTITUTE(R). To learn more about this comprehensive and award winning educational resource, please visit TheWoundInstitute.com(R). HEALTHPOINT is a DFB Pharmaceuticals, Inc. affiliate company, and is based in
SOURCE HEALTHPOINT, Ltd.
