Central Laboratory
Analytical services are an integral part of the drug and medicines development process. Simbec Central Laboratory Services provides essential supporting analyses for Phase I-IV trials; these services are designed exclusively for the Pharmaceutical industry.
Our combination of expertise and experience enables us to provide a rapid, reliable and responsive service ensuring all results provided are precise and delivered on schedule.
Simbec assigns dedicated Project Leaders as part of its service plan, who support trial implementation, review testing and any trial-specific protocol requirements and design a laboratory schedule. These Project Leaders maintain ongoing communication with the Study Manager until trial completion.
We understand the need for rapid results and are committed to expedited analysis and electronic results transfer (upon authorisation) to ensure our sponsors are able to access their information as quickly as possible.
Our fully equipped GLP/GCP compliant laboratories deliver quality assured data, effective sample transport, sample tracking and comprehensive data and management reports all prepared with confidentially in mind. Our service boasts:
- Extensive range of analytical capabilities
- Dedicated, experienced staff
- Round-the-clock analyses - 7 days a week
- 21 CFR part 11 compliance
- State-of-the-art refrigerator and freezer temperature monitoring system
- Rapid turnaround times
- Biomarker services
- Internal QA support
- Pharmacokinetic and Pharmacodynamic analyses
- Logistics management
- Visit-specific sample collection kits
- Protocol-specific pathology manual
- Project Management
- Data Management
