Submit an RFI
To request more information about our clinical and safety data services including clinical data management, biostatistics, medical writing, clinical programming, and pharmacovigilance services, please complete the form below. A member of Quanticate’s Business Development team will then contact you within 2 days.
The three steps to a faster drug approval
1. Submit an RFI
- Secure a meeting with our experts
- Put in place a CDA/NDA
- Specify your needs and requests
- Our specialist will guide you to a tailored outsourcing solution
2. Part of your team
- Kick-off meeting and selection of the preferred approach
- Quanticate resources assigned to your team according to your preferred resource model
- Focused on customer satisfaction and quality via our 'Coded To Care' Mantra
3. Your Drug is Approved!
- All your data integrity and quality has improved
- Your regulatory submission was a success
- You improved study efficiency and reduced timelines
- A new partnership is formed, and we are committed to improving your clinical data for future studies
Submit a Request for Information
Receive information on how our clinical and post-marketing solutions
can support your trial!
Submit an RFI
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