Since 1994, McCulley/Cuppan experts have:
- Worked with more than 60 pharmaceutical and medical device companies worldwide.
- Supported more than 40 project teams in all the major therapeutic areas.
- Trained over 8,000 pharmaceutical and medical device professionals.
- Developed customized training solutions for over 40 client organizations around the world.
- Reviewed and written hundreds of regulatory documents.
- Consulted to FDA on improving report writing quality and meeting management.
- Conducted numerous interviews with regulatory authorities in the US and Europe regarding submission document usability.
For more details about our experience, please view our Statement of Qualifications Presentation.
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