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Catalent Pharma Solutions offers comprehensive regulatory, clinical and product development consulting services to help minimize your product's development time and maximize your product's time on the market. With global strategic expertise that extends from the US to European, Asian, Canadian and South American markets, our consultants can provide the solutions to help bring your product to market faster.
Catalent's regulatory and clinical experts have a wide range of in-depth experience with both established and novel pharmaceutical dosage forms across a wide range of therapeutic areas. The global regulatory services group has an extensive consulting portfolio. Our services include:
- Worldwide scientific and regulatory strategies
- Project management
- General scientific advice
- Non-clinical and clinical planning and project management
- Regulatory submissions at investigational and marketing stages
- CTD Compilation
- Regulatory compliance and audits
- Technical and medical writing
- Regulatory due diligence
- Regulatory electronic publishing
- Training workshops
To learn more about our regulatory, clinical and training capabilities, download our brochure.
For capabilities that meet your needs, and outcomes that exceed your expectations, call Catalent today. For more information, please fill out our contact us form or call a member of our sales staff at +1 866.720.3148.