William Pfister Email & Phone Number
Senior Director Development Regulatory Affairs @ Acorda Therapeutics, Inc.
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William Pfister Location
- Trenton, NJ, US
William Pfister Work
- 2012 -now Senior Director Development Regulatory Affairs @
- 2012 -2012 Consultant, Drug Development and Regulatory Affairs @ Pfister Consulting
- 2011 -2012 Senior Director, Regulatory Affairs @ Aprecia Pharmaceuticals Company
- 2009 -2011 Senior Director, Product Development Consultant @ Burke Pharmaceutical Research, Inc.
- 2010 -2011 Director, Regulatory Affairs @ Sonar Products, Inc.
- 2009 -2009 Vice President, Scientific Affairs @ NAL Pharmaceuticals
- 1999 -2008 Senior Director, Product Development, Preclinical and Regulatory Affairs @ NexMed (U.S.A.), Inc.
- 1998 -1999 Director Product Development and Project Management @ Lavipharm Laboratories
- 1992 -1998 Director Regulatory Affairs and Quality Assurance, Project Management and Transdermal Development @ PharMetrix Division of TCPI (formerly Division of PharmaPatch PLC and PharMetrix
- 1983 -1992 Senior Scientist, Manager Controlled Release laboratory @ Dow Corning Corp., Medical Materials Business
- 1980 -1983 Senior Research Investigator @ American Critical Care
- 1978 -1980 Supervisor, Senior Scientist Quality Control Department @ Hoffman-La Roche, Inc.
William Pfister Education
- Purdue University
Ph.D. (Pharmacology & Toxicology)
1976-1978 - Purdue University
Master of Science (M.S.) (Pharmacology & Toxicology)
1974-1976 - University of New Hampshire
Bachelor of Science (B.S.) (Biochemistry)
1971-1973
William Pfister Skills
- Directory Pharmaceutical Regulatory Affairs
- Pharmaceutical Management Executive - Global Regulatory Strategies
- Regulatory Affairs
- Regulatory Submissions (INDs, ANDAs, NDAs, eCTDs)
- Regulatory Compliance (GLPs, GCPs, GMPs, ISO)
- Product Development
- Transdermal and Topical Product Development
- Intraoral Drug Delivery Systems
- Chemistry Manufacturing Controls (CMC)
- Program - Project Management
- Preclinical Toxicology (acute, subacute, chronic,etc.)
- Clinical Research
- Clinical Trials (Phase 1, 2 and 3)
- Bioequivalence and Bioavailability Studies
- Consumer Product Safety Testing (CPSC)
- Child Resistant Package Testing (16 CFR 1700.20)
- M&A Due Diligence
- Expert Witness Patent Litigation
- Regulatory Submissions
- Clinical Development
- Clinical Trials
- Analytical Chemistry
- IND
- Drug Delivery
- CMC
- FDA
- Toxicology
- GCP
- Pharmaceutical Industry
- Drug Development
- Due Diligence
- Lifesciences
- GLP
- GMP
- CRO
- R&D
- NDA
- Validation
- Pharmacology
- Quality System
- Biotechnology
- Technology Transfer
- In Vitro
- Pharmaceutics
- Quality Assurance
- Medical Devices
- Pharmacokinetics
- Protocol
- In Vivo
- Pharmacovigilance
- Subacute
- Preclinical Toxicology Acute
- 2 and 3
- ISO
- Ndas
- Etc
- Strategic Planning
- Chemistry Manufacturing Controls Cmc
- Management
- Leadership
- Regulatory Compliance Glps
- GCPs
- Andas
- Project Management
- Marketing
- Pharmaceutical Management Executive
- Clinical Trials Phase 1
- Chronic
- Ectds
- Consumer Product Safety Testing Cpsc
- Regulatory Submissions Inds
- Gmps
- Program
- Global Regulatory Strategies
- Key Opinion Leaders
- Pharmaceutical Research
- Salary
- Adobe Contribute
- Cardiovascular
- Stability Testing
- Guidelines
- Flexible
- Conceptual Modeling
- Informatics
- Cream
- Brochures
- Investigation
- Executive Management
- Social Influence
- Commercialization
- Program Management
- Testing
- Collaborative
- Google Groups
- Draft
- Erectile Dysfunction
- Applications
- Rabbit
- Conferences
- Communication
- Commercial Products
- Assurance
- Angina
- Project Planning
- Editing
- Optimization
- Respiration
- Kinetics
- Regulatory Filings
- Medicine
- FIX Protocol
- Strategies
- Cac
- USP
- Acting
- Cell
- Maa
- Internal Audit
- Publications
- Design
- Hazardous Materials
- Product Promotion
- Phase 1
- Technical Support
- Monitors
- Filing
- Critical Care
- Characterization
- Springs
- Aid
- Silicones
- Track Record of Success
- Distillation
- Short
- Intelligence
- Technical Marketing
- Monographs
- Entrepreneurship
- Product Safety
- Nds
- Pharmacy
- Dissolution
- Meetings
- Quality Control
- Dermatology
- Risk Assessment
- Contractual Agreements
- SPC
- Compliance
- Project
- Manufacturing
- Assessment
- Intellectual Property
- Ingredients
- Fax
- Ultra
- American
- Diffusion
- International Regulations
- Tk
- Labelling
- Diagnostics
- Sexual
- Dental Products
- Successful Track Record
- Schedules
- Study Reports
- Cosmetics
- Technical Reports
- Sot
- Interpretations
- Inactive
- Glaucoma
- Document Management
- Portfolio Management
- Toxicity
- Line Extensions
- Legislation
- Letters
- Therapists
- Non Clinical
- Spl
- Interviews
- Internet Protocols
- Active
- Project Portfolio Management
- Indications
- Ise
- Point of Contact
- Glucose
- Coordinated
- Problem Solving
- Illness
- Business Planning
- Nih
- Hospitals
- Rx
- Vendors
- Clinical Protocols
- Psychology
- Fine Chemicals
- High Performance Computing
- Complaints
- Safety
- Development Programs
- Agents
- Analysis
- Trademarks
- ANDA
- Engineering Process
- Compliance Reporting
- Risk
- Controlled Release
- Documentation
- Lacquer
- Manuscript
- Reconcile
- Consulting
- Regulations
- Forms
- Wound Care
- Prevention
- Cros
- Software Lifecycle
- Treatment
- Bonus
- Guidance
- Materials
- Home
- Prototype
- Mobilize
- Amendments
- Patents
- Regulatory Compliance
- Qualification
- Waivers
- Legal Writing
- Female
- Business Development
- Approvals
- Hygiene
- Project Leadership
- International
- Adhesives
- Scientists
- Process Improvement
- Radiation Safety
- Novartis
- Regulatory Intelligence
- Obtain
- Essential Oils
- C
- Proof of Concept
- Budgets
- R
- Technical Information
- Sop
- Timelines
- Laptops
- SAN
- Change Control
- Microbiology
- Annual Reports
- Profiles
- Responsibility
- Facilities Management
- Managing Product Development
- Proposal Writing
- Regulatory Agencies
- Attract
- Oracle RAC
- Citizenship
- Strategy
- Early Development
- Stability
- Regulatory Filing
- Cardiovascular Disease
- Technical Presentations
- Yahoo
- Project Teams
- Writing
- Compensation
- Technical Liaison
- Usa
- Reproductive
- Advertising Agency
- Registrations
- Business Perspective
- Ctm
- Laboratory
- Diplomate
- Biochemistry
- Skin
- Statistical Analysis Plans
- Detail
- Transdermal
- Abstracts
- Rights
- Central Nervous System
- Iss
- ICH guidelines
- Handling Money
- OTC
- Evaluation
- Supplements
- Dossiers
- Posters
- Injury
- Clinical Manufacturing
- Film
- Autodesk Inventor
- Microsoft Office
- Fashion
- Contractors
- Supplies
- Radioactive Materials
- Chemical
- Presentations
- Risk Management
- Efficacy
- Data Management
- Briefing
- Bulk
- Resume
- Human Resources
- Reports
- Negotiation
- Scientific
- Infusion Pumps
- Coordinate
- Pipelines
- Research
- Annual Budgets
- Canada
- Delivery
- Comprehension
- eCTD
- Formulation
- Emissions Trading
- Microsoft Excel
- Antifungal
- Cfr
- Chemistry Manufacturing Controls
- Preclinical Toxicology
- Child Resistant Package Testing
- Consumer Product Safety Testing
William Pfister Summary
- William Pfister, based in Trenton, NJ, US, is currently a Senior Director Development Regulatory Affairs at Acorda Therapeutics, Inc.. William Pfister brings experience from previous roles at Pfister Consulting, Aprecia Pharmaceuticals Company, Burke Pharmaceutical Research, Inc. and Sonar Products, Inc.. William Pfister holds a 1976 - 1978 Ph.D. in Pharmacology & Toxicology @ Purdue University. With a robust skill set that includes Directory Pharmaceutical Regulatory Affairs, Pharmaceutical Management Executive - Global Regulatory Strategies, Regulatory Affairs, Regulatory Submissions (INDs, ANDAs, NDAs, eCTDs), Regulatory Compliance (GLPs, GCPs, GMPs, ISO) and more. William Pfister has 2 emails on RocketReach.
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Top Acorda Therapeutics, Inc. Employees
Jonathan Kuhn
Director of Global and Brand Marketing
Monsey, NY, US
Bill Dollard
Vice President
Hawthorne, NY, US
Denise Duca
Sr. Vice President - HR
Pleasantville, NY, US
Mike Marrah
Regional Business Director
Akron, OH, US
Anthony Michael
Executive Director - Litigation
New York, NY, US
Kevin Lacey
Executive Director, Legal Affairs
Hawthorne, NY, US
Diane Urbanowicz
Executive Director
Butler, NJ, US
Shuofei Gao
Director Program Management
Granite Springs, NY, US
Mark Pinney
CFO
New York, NY, US
Farzin Daneshnia
Director of Market Development
Los Angeles, CA, US
Pamela Barry
Associate Director Quality Assurance
Ossining, NY, US
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