Biomedical Engineer and Quality Assurance Expert, Jeffrey P. Taub, Joins NDA Partners as Expert Consultant

ROCHELLE, Va., May 27, 2020 /PRNewswire-PRWeb/ -- NDA Partners Chairman Carl Peck, MD, announced today that Jeffrey Taub, a biomedical engineer with more than 25 years of experience in product design, development, and manufacturing of medical devices and combination products, has joined the firm as an Expert Consultant. His expertise includes quality assurance, including ISO 13485 and FDA QSR (21 CFR 820), risk-based product development (ISO 14971), design controls and design verification, human factors and usability (ISO 62366), and supply chain and CMO management.

Throughout his career, he has successfully designed, launched, and marketed more than a dozen medical devices including single and multichannel LVP infusion pumps, intraoral dental imaging systems, intravascular cooling systems, ultrasound imaging and ablation devices, an interferential pain management (TENS) product, a DNA sequencing sample prep instrument, and an RF ablation surgical cutting product.

Most recently, Mr. Taub served as Senior Technical Project Manager and Director of Product Development at Paramit Product Development. Prior to joining Paramit, he served as Vice President of Research and Development at Surgitech Surgical Technologies, Director of Device Engineering at Vital Therapies, Inc., and Senior Program Manager and Engineering Manager at BIT Group USA (formally Paragon MedSystems and California MedTech).

According to Dr. David Feigal, manager of NDA Partners' medical device practice, "Mr. Taub's experience in product design, development, and manufacturing, in addition to his expertise in quality assurance, risk-based product development, and design controls and verification, will bring significant benefits to our clients developing medical device and combination products. We are pleased to welcome him to NDA Partners."

Mr. Taub earned his bachelor's degree in biomedical engineering from Boston University's College of Engineering.

About NDA Partners
NDA Partners is a life sciences management consulting and contract development organization (CDO) focused on providing product development and regulatory services to the pharmaceutical, biotechnology, and medical device industries worldwide. The highly experienced Principals and Expert Consultants in NDA Partners include three former FDA Center Directors; the former Chief Executive Officer and Chief Science Officer at the United States Pharmacopeial Convention (USP); an international team of more than 100 former pharmaceutical industry and regulatory agency senior executives; and an extensive roster of highly proficient experts in specialized areas including nonclinical development, toxicology, pharmacokinetics, CMC, medical device design control and quality systems, clinical development, regulatory submissions, and development program management. Services include product development and regulatory strategy, expert consulting, high-impact project teams, and contract management of client product development programs.

Earle Martin, Chief Executive Officer
Office: 540-738-2550