George De La Rosa
Independent Regulatory Affairs Consultant (Support & Submissions) at Rapid RA Consulting, LLC | Port Hueneme, California, United States
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Independent Regulatory Affairs Consultant (Support & Submissions) at Rapid RA Consulting, LLC in January 2024 to Present
Independent Regulatory Affairs Consultant at Part - Time Independent Regulatory Affairs Consultant – Medical Device Industry in June 2017 to December 2023
Regulatory Affairs Professional at Bio-Rad Laboratories in September 2017 to July 2023
Regulatory Affairs Professional at NeuroPace in June 2015 to September 2017
Regulatory Affairs Professional (Consultant) at Real Staffing Group, a trading division of Specialist Staffing Solutions Inc. in August 2014 to May 2015
Regulatory Affairs Professional at Edwards Lifesciences in August 2013 to August 2014
Regulatory Affairs Professional at Ventana Medical Systems in September 2009 to August 2013
Director, Regulatory Affairs (Consultant) at Reglera LLC in April 2008 to April 2009
Sr. Project Manager, Regulatory Affairs at Biotronik in November 1997 to March 2008
Director of RA & Engineering at Redman Powerchairs in February 1992 to October 1997
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Degree in Electrical Engineering - State University of New York Buffalo, Bachelors of Science in Electrical Engineering, Electrical Engineering, June 1988 to June 1990
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International Regulations
Recalls
Coordinate Meetings
Regulatory Operations
Regulatory Projects
Transparency
Technical Reports
Regulatory Audits
Legal Compliance
Design Review
Diversity
Presentation Skills
Timelines
Written Communication
Regulatory Approvals
Regulatory Standards
Remediation
Managed Detection and Response (MDR)
Cardiovascular Disease
Creative Problem Solving
Clinical Assessment
Relationship Development
Defining Requirements
Critical Thinking
Organization Skills
Regulatory Guidelines, organizational skills
Regulatory Guidelines, submissions
Preventive Actions
Literature Reviews
Complex Project Management
Product Registration
Package Inserts
Marketing Materials
Client Relations
Resiliency
Implantable Medical Devices
Class III Medical Devices
QSR
Analytical Skills
Knowledge Sharing
Technical Files
Launch Operations
User Requirements
Technical Requirements
Regulated Industry
Attention to Detail
Product Strategy
Regulatory Interactions
Presentations
Establishing Processes
Clinical Protocols
Regulatory Filings
Strategic Planning
Setting Strategic Direction
Skill Development
Creative Ideation
Technical Writing
Multi-country
Strategic Management
Remote Work
Regulatory Agencies
Communication
Regulatory Strategy
Medical Devices
PMAs
FDA
Regulatory Affairs
Problem Solving
Product Development
510 K
Diagnostics
GMP
Regulatory Submissions
Strategy
Cross-functional Team Leadership
Clinical Trials
CAPA
R&D
ISO 13485
Biotechnology
Design Control
Commercialization
Quality System
Hardware Diagnostics
Lifesciences
Clinical Research
Product Launch
PMA
Validation
Cardiology
Assay Development
Regulatory Requirements
Quality Control
21 CFR Part 11
CE marking
Clinical Development
Life Sciences
Premarket Approval (PMA)
Research and Development (R&D)
U.S. Food and Drug Administration (FDA)
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What is George De La Rosa email address?
Email George De La Rosa at [email protected]. This email is the most updated George De La Rosa's email found in 2026.
What is George De La Rosa phone number?
George De La Rosa phone number is 5186439427.
How to contact George De La Rosa?
To contact George De La Rosa send an email to [email protected]. If you want to call George De La Rosa try calling on 5186439427.
What company does George De La Rosa work for?
George De La Rosa works for Rapid RA Consulting, LLC
What is George De La Rosa's role at Rapid RA Consulting, LLC?
George De La Rosa is Independent Regulatory Affairs Consultant (Support & Submissions)
What industry does George De La Rosa work in?
George De La Rosa works in the Biotechnology industry.
George De La Rosa Email Addresses
George De La Rosa Phone Numbers
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