- One point of contact:
- For regulatory preparation and submission and
- For contract and budget negotiation
- Experienced CRCs on site, skills and certification in all study types
- Dedicated regulatory staff to handle all regulatory requirements
- Back-up staff for all sites to ensure adherence to timelines
- Standardized SOPs and site staff training
- Database of 100,000+ potential clinical participants
- Network of experienced investigators in numerous therapeutic areas
We work closely with your team to ensure successful trial execution!
In the clinical trial business since 2005, Viable is a reliable, reputable partner for your next clinical trial.