2003 -now Vice-President, Regulatory Affairs and Quality Assurance @
1982 -2004 Founder and President @ Steinman Associates
1972 -1981 Manager and Director of Quality Assurance, Consultant @ New England Nuclear Corporation/Dupont
Steve Steinman Education
University of Southern California, School of Law
Certificate (Food and Drug Law)
1968-1968
University of California
A.B. (Zoology, Molecular Biology)
1956-1961
Steve Steinman Skills
Drug Development
CTMS
IND
FDA
Regulatory Affairs
NDA
Lifesciences
Sop
Biopharmaceuticals
Medical Devices
Pharmaceutical Industry
Clinical Development
Quality Assurance
Oncology
21 CFR Part 11
In Vitro
Technology Transfer
GLP
Regulatory Submissions
Clinical Trials
Drug Discovery
CRO
GCP
Biologics
Biotechnology
Pharmaceutics
GMP
Life Sciences
Validation
Clinical Trial Management System Ctms
u.s. Food and Drug Administration Fda
Cancer
Standard Operating Procedure Sop
New Drug Application Nda
New Drug Application
u.s. Food and Drug Administration
Clinical Trial Management System
Standard Operating Procedure
Steve Steinman Summary
Steve Steinman, based in Tucson, AZ, US, is currently a Vice-President, Regulatory Affairs and Quality Assurance at Amplimed Corporation. Steve Steinman brings experience from previous roles at Steinman Associates and New England Nuclear Corporation/Dupont. Steve Steinman holds a 1968 - 1968 Certificate in Food and Drug Law @ University of Southern California, School of Law. With a robust skill set that includes Drug Development, CTMS, IND, FDA, Regulatory Affairs and more. Steve Steinman has 1 emails and 1 mobile phone numbers on RocketReach.
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