Judy H Martin

Regulatory Affairs Consultant

We found the following information about Judy H Martin at Opus Regulatory, Inc., where Judy H Martin has worked as a Consultant since 2016. Judy's total work experience is over 23 years, during which time this expert had at least five jobs at different companies to develop professional skills. Judy attended school at the University of Nc - Greensboro. This expert has the following certificates: Rac, Mt(Ascp), Regulatory Affairs Professionals Society (Raps), and American Society of Clinical Pathologists. Los Angeles, California is the place where this person currently lives. You can search for Judy's email address and phone number. We can also provide you with detailed contact information upon request.
Name variants:
Judith Martin
Last updated May 30, 2024

Contact Information

Last Update
Jul 14, 2022
Email
ju**@jhmartin.org
Location
Los Angeles, CA

Workplace

Opus Regulatory, Inc.
Consultant

Boston, MA

Industry

Pharmaceuticals, Employment Agency

Work History

Consultant

225 Franklin St, Boston, MA 02134
Founded in 1994, Opus Regulatory, Inc. (Opus) is a highly specialized contract consulting firm dedicated to the Regulatory Affairs profession. Headquartered in Boston, we serve biopharmaceut...
Mar 2016 — May 2017

Regulatory Affairs Project Manager

Franchise expert on product and marketing claims development and substantiation Review and approval of promotional and educational material Create and present training programs for Market...
May 2002 — Sep 2011

Regulatory Affairs Manager

Responsible for domestic and international submissions for a minimally invasive cardiovascular surgical device company.
Sep 2000 — May 2001

Senior Regulatory Affairs Specialist

20 Valley Stream Pkwy, Malvern, PA 19355
Develop and implement regulatory strategies for new and modified products Prepare complex 510(k)s and regulatory rationales that included clinical studies Review and approve domestic and ...
Jan 1993 — Sep 2000

Regulatory Affairs Analyst

Prepared 510(k) submissions, coordinated recalls and reviewed product labeling. Also conducted customer complaint investigations, patient incident investigations and filed MDRs. Prior to joi...
Feb 1987 — Dec 1992

Occupations

Counselor
Doctor of Medicine
Speaker
Advisor
Spokesperson
Representative

Skills

Technical Writing
Regulatory Affairs
Regulatory Compliance
Compliance
Medical Devices
Validation
Fda
Regulatory Submissions
Iso 13485
Process Improvement
Design Control
Regulatory Requirements
Gmp
Capa
Quality System
V&V
Sop
Product Development
Quality Assurance
Iso 14971
U.s. Food and Drug Administration
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