David Pudwill Email & Phone Number
Principal Consultant @ FDA Blueprint
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David Pudwill Location
- Orlando, FL, US
David Pudwill Work
- 2024 - now Principal Consultant @
- 2021 - now Principal Consultant @
- 2025 - now President and CEO @
- 2024 - now Instructor, Regulatory Submissions for Medical Devices @
- 2023 - now Medical Sales Director @
- 2021 - 2023 Senior Vice President, Head of Regulatory Affairs @
- 2020 - 2021 Senior Director, Regulatory Affairs @
- 2020 - 2021 Professor @
- 2018 - 2020 Senior Director, Ostomy Franchise Regulatory Affairs and Quality Assurance @
- 2017 - 2018 Director, Regulatory Affairs and Quality Assurance, Americas @
- 2008 - 2017 Lead Medical Device Reviewer, Biomedical Engineer @
- 2015 - 2016 Chief (Acting), Implantable Electrophysiology Devices Branch @
- 2015 - 2015 Congressional Affairs Specialist (Detail) @
- 2006 - 2007 Field Engineer @
- 2005 - 2005 Summer Research Intern @
David Pudwill Education
- Harvard Business School Online
Other; "CORe: Credential of Readiness"
2016 - 2016 - The Johns Hopkins University
Master's degree (Mechanical Engineering)
2011 - 2014 - Case Western Reserve University
Bachelor of Science (BS) (Biomedical Engineering)
2002 - 2006 - Eastview High School
David Pudwill Skills
- Strategic Thinking
- Workload Prioritization
- Electronic Common Technical Document (eCTD)
- Pre-clinical Studies
- Analytical Skills
- Negotiation
- Written Communication
- Teamwork
- Resource Allocation
- Relationship Development
- Regulatory Agencies
- Oncology
- Immunology
- Clinical Trials
- ODD
- Pharmaceuticals
- Registration
- Asset Life Cycle Management
- Setting Strategic Direction
- Rare Diseases
- Regulatory Law
- Biotechnology
- Standard Operating Procedure (SOP)
- Pharmaceutics
- Good Manufacturing Practice (GMP)
- Lead Qualification
- Customer Satisfaction
- Attention to Detail
- Business Development
- Thought Leadership
- Strategic Leadership
- Critical Thinking
- Technical Documentation
- Regulatory Documentation
- QSR
- Presentations
- Marketing Compliance
- 21 CFR
- Management
- Leadership
- Leadership Development
- Project Management
- Engineering
- Product Development
- Data Analysis
- Biomedical Engineering
- Medical Devices
- FDA
- Clinical Research
- Public Speaking
- Cross-functional Team Leadership
- Policy
- Regulatory Affairs
- Health Policy
- Government
- Strategic Planning
- Research
- Team Leadership
- Photographic Lighting
- Photography
David Pudwill Summary
- David Pudwill, based in Orlando, FL, US, is currently a Principal Consultant at FDA Blueprint. David Pudwill brings experience from previous roles at Mr Regulatory, Prather Biomedical Corporation, UC San Diego Extended Studies and Prather Ranch. David Pudwill holds a 2016 - 2016 Other; "CORe: Credential of Readiness" @ Harvard Business School Online. With a robust skill set that includes Strategic Thinking, Workload Prioritization, Electronic Common Technical Document (eCTD), Pre-clinical Studies, Analytical Skills and more. David Pudwill has 6 emails and 1 mobile phone numbers on RocketReach.
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