Paul Mason

Class Iii Medical Device Regulatory and Clinical

Paul Mason is a high-level professional, working in Self-employed Medical Device Consultant as a Class III Medical Device Regulatory/Clinical/Quality Professional since 2011. This person has earned professional experience in more than seven positions at various companies. Paul Mason went to the Duke University and was studying there. San Diego, California is the area, where this person was known to settle. Paul's email address and phone are easily accessed through SoftwareOfficial by request.
Name variants:
Pauly Mason, Pablo Mason
Last updated Jun 12, 2024

Contact Information

Last Update
Jul 13, 2022
Email
pm**@cox.net, pm**@ix.netcom.com, pm**@imtheramedical.com
Location
San Diego, CA
Company
Self-employed Medical Device Consultant

Workplace

Class III Medical Device Regulatory/Clinical/Quality Professional

Work History

Class III Medical Device Regulatory/Clinical/Quality Professional

Class III Medical Device Regulatory Affairs, Quality and Clinical. Extensive IDE and PMA experience
from Feb 2011

Sr Director, Regulatory Affairs

Apr 2009 — Feb 2011

VP, Regulatory Affairs/Quality Assurance

2005 — 2008

Director, Regulatory Submissions

1998 — 2005

VP, Regulatory Affairs

1997 — 1998

Manager, Regulatory Submissions

1992 — 1997

Sr Reg Analyst/Biostatistican/CRA

1987 — 1992

Occupations

Executive
Director
Operations Manager

Skills

Regulatory Affairs
Regulatory Submissions
Medical Devices
Fda
Pma
Design Control
Iso 13485
Validation
Clinical Research
Gmp
Capa
Regulations
V&V
Biotechnology
Iso 14971
Quality System
21 Cfr Part 11
Glp
Clinical Trials
Pharmaceutical Industry
Fda Gmp
Change Control
Clinical Development
Ce Marking
Regulatory Requirements
Hardware Diagnostics
Biomedical Engineering
Quality Auditing
Sop
Lifesciences
Sterilization
R&D
Leadership
Quality Assurance
Life Sciences
Gcp
Commercialization
U.s. Food and Drug Administration
Technology Transfer
Cqa
Catheters
Premarket Approval
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