Find The Right CRO For Your Next Trial
We have combed the world for the best CROs, CSOs, and patient populations available anywhere. Each of our CRO partners have been thoroughly screened and have previously worked for the largest pharma and biotech companies in the world. Let us introduce you! Click on their logo to learn more!
Community Research
Services: Phase 1 - 2a
Location: Cincinnati, Ohio
Community Research has access to a significant number of patients (large database of 40,000+) in a variety of therapeutic areas:
- Healthy Subjects (>31,000)
- Healthy Elderly Subjects (>3,300)
- Depression (>9,200)
- Hypertension (>2,800)
- Insomnia (>2,200)
- Diabetes (>1,200)
Vimta Labs
Services: BA / BE, Phase 2 - 4
Location: Hyderabad, India
- 240 bed facility with huge bioanalytical lab
- Reduce clinical and bioanalytical costs by at much at 50%
- 4 successful FDA audits
- Not affiliated with a pharmaceutical company
HungaroTrial
Services: Phase 1 - 4
Location: Budapest, Hungary
HungaroTrial is unique in offering a patient enrollment guarantee:
If HungaroTrial cannot complete the enrollment within the timeline, there will be no further monthly fee until the enrollment is completed.
GVK BIO
Services: Phase 2 - 4, BA / BE
Location: Hyderabad, India
- Comprehensive Pharmacovigelence Services for Generic and Innovator Companies
- Full Service clinical trials across a broad therapeutic area including Oncology and Infectious Diseases
- Comprehensive Medical Writing Services from stand-alone deliverables to full service program outsourcing
Services: Phase 2 - 4
Location: Sao Paulo, Brazil and Lisbon, Portugal
- Unparalleled access to Latin American patients helping clients exceed enrollment targets & timelines
- Reduced costs – 70% of per/patient cost compared to the USA
- Increased market share and margins by increasing proposal hit rate and consistently bringing trials in on time and on budget
- Close relationship with ANVISA – Brazilian regulatory agency facilitates communication and cooperation
- Access to special populations including pediatric and ethnic Japanese
- Download Free Whitepaper: Overview of Latin America and Brazil
Services: Phase 1 - Pharmacology
Location: Belfast, Northern Ireland
- 14 Day Regulatory Approval - sponsors see regulatory approval in 14 days after submission - one of the fastest processes in the world
Swiss Pharma Contract (Covance)
Services: Phase 1 - 2a
Location: Basel, Switzerland
- Swiss Pharma Contract requires no IND and no IMPD
- 30 day approval cycle
- The only country allowing case-by-case basis, first in man biological testing on healthy subjects
AXIS Clinicals
Services: BA / BE, Phase 2 - 4
Location: Hyderabad, India
- AXIS Clinicals has the unique ability in India to dose females on a routine basis. These bio studies may be 100% female studies (including post menopausal) or mixed gender studies which will enhance FDA submissions.
- 292 beds; 16 LC/MS/MS
- 3 successful FDA audits in the past 2 years. The latest successful FDA audit was in October 2009 and no 483's were issued.












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