Thom Wehman is a qualified professional, that works in adel Engineering Consultants on the position of Founder since 2010. Thom Wehman has earned professional experience in more than nine positions at various companies. Thom Wehman went to the Michigan State University and was studying there. This expert has such professional qualifications as Regulatory Affairs Professional, Quality Assurance Engineer, and Quality Auditor. Berkeley, California is the city, where this expert was known to be living. Their phone number and email can be accessed through this website on demand.
Name variants:
Thom Wehman
Last updated Jun 15, 2024
Contact Information
Last Update
Jul 11, 2022
Email
tw**@comcast.net
Location
Berkeley, CA
Company
adel Engineering Consultants
Workplace
Founder
Work History
Founder
Consulting for Operations, Regulatory Affairs, Pre-clinical studies, QA and Document Control in Medical Device field.
from Oct 2010
President & COO
Medical device Gastroenterology Company for non-invasive treatment of overweight and obesity. Lead R & D teams, Manufacturing, QA, Marketing/ Sales, Pre-Clinical, Clinical and Regulatory...
Sep 2007 — Oct 2010
President
Consulted for:
Aesthetic and Reconstructive surgery: Alase (laser), Vidaderm
Cardiovascular-stents (drug coated and uncoated): A-Med, Abbott Vascular, NeoMend, Aptus Endosystems, Atricure, C...
Oct 1992 — Sep 2007
Head of Regulatory Afair, Document Control & QA
Medical device start-up company specializing in urinary incontinence treatment. Responsibilities included regulatory affairs, quality and document control. Responsible for converting regulat...
2001 — 2003
Head of Regulatory Affairs, Document Control & QA
Medical device start-up company specializing in Gastroesophageal reflux disease. Responsibilities included regulatory affairs, quality and document control. USA pre-clinical studies and assi...
1998 — 2001
President/COO
Medical device start-up company specializing in electrosurgery and cardiology. Responsibilities included, regulatory affairs, quality, clinical affairs, engineering, manufacturing, research...
1997 — 1998
Operations and VP regulatory Affairs, QA and Document Control
Medical device start-up company specializing in canser. Responsibilities included regulatory affairs, quality and document control. USA pre-clinical studies and assisted with South American ...
1996 — 1997
VP Operations, Regulatory Affairs, QA, Document Control
Co-Founder of ear, nose and throat company Responsible for multiple 510(k)âÃÂÃÂs, quality system site license and FDA audit. Performed pre-clinical and OUS clinical site selection and...
1995 — 1996
VP Regulatory, QA, Document Control
Co-Founder of ear, nose and throat company Responsible for multiple 510(k)âÃÂÃÂs, quality system site license and FDA audit. Performed pre-clinical and OUS clinical site selection and...
1993 — 1995
Occupations
Executive
Founder
Chairperson
Chief Operating Officer
Doctor
Gastroenterologist
Chief Executive Officer
Founding Member
Chief Executive
General and Operations Manager
Physician
Corporate Executive
Skills
Electronic Submissions
Halt
Chemistry
Failure
Reliability
Fda
Validation
Regulatory Affairs
Iso 13485
Medical Devices
Quality System
Quality Assurance
R&D
Product Development
Capa
Clinical Trials
Cardiology
Clinical Development
Strategy
Clinical Research
Cross Functional Team Leadership
Ce Marking
Design Control
Entrepreneurship
Software Documentation
Manufacturing
Start Ups
Oncology
Commercialization
Biotechnology