Clinical Research Services
Through the Clinical Research Services (CRS) division, BBL offers a full suite of clinical trial management services from initial study design to final regulatory submissions. As a full service Contract Research Organization (CRO), CRS has successfully completed clinical validation studies in the United States, Africa, Europe, Asia and South America. BBL offers a full 'turnkey' approach to outsourcing clinical validation studies. BBL’s proprietary network of principal investigators, enables CRS to rapidly identify the most significant and rare global patient populations and decrease the time to market of products. BBL’s full service central laboratory services provides the value-added testing necessary to demonstrate clinical efficacy.
CRS offers a complete suite of clinical trial management services, including:
- The development of HIPAA-compliant informed consents, collection protocols and CRFs
- Institutional Review Board (IRB), Independent Ethics Committee (IEC) and Ministry of Health (MOH) submissions, globally
- Site selection, initiation and monitoring, utilizing our global PI Network.
- On-site sample management and logistical support
- Short- and long-term storage of samples in the Bio-Repository
- Central laboratory services, including parallel testing
- Management and analysis of data collected during the study
- Consulting services to prepare submissions to relevant regulatory bodies, such as the US Food & Drug Administration (FDA)
For more information on BBL’s Products and Services, please click here.
If you are planning a clinical trial soon, consider allowing BBL to manage all or part of your clinical trial as a time and cost-saving alternative to managing the trial in-house. Please contact us directly to see how BBL can improve your time to market. |
