400+ hospitals as part of our current client portfolio
We Deliver
Your clinical research partner
We collaborate with pharmaceutical firms, biotech firms, clinical research facilities, clinical research organizations (CROs), and other businesses to help them deliver their research quickly, reliably, comprehensively, ethically, & accurately.
Fastest growing SMO in the country
Fast facts
400+ potential sites, 10+ U.S FDA audited sites, large team of experienced and expert clinical research coordinators.
How are we different
Why us ?
- Well-established quality management System with operations to be carried out by established standard operating Procedures
- Our personnel trained and educated in both clinical and administrative elements.
- With thorough monitoring and a strong focus on each project
- Guidance throughout the study project making clinical trial site management more efficient
- We wish to create a fully integrated network of field and patient service centers that will help your business.
Our methodology
Phases we manage
– Phase I to IV trials
– ICH GCP Guidlines
– Clinical Trial Design Preparation
– Pre Trial Preparation
– Active Trial Functioning
– Study close out/ termination preparation
Comprehensive geographical coverage
Our network
Our studies
THERAPEUTIC AREAS
Let experts handle your projects
Our team
- Medigence has a team of certified specialists with expertise in clinical research.
- Team with a diverse range of skills with excellence in communication and have ability to build effective relationships with strong focus.
- Offering competent CRO services.
- We are a team of Investigators, Co-Investigators, Study Coordinators, Nurse, Pharmacist, Phlebotomists, and Technicians.