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Sipra Labs has the best team of clinical experts associated with each of its projects. Sipra, as an international Contract Research Organization offers varied services with thrust on clinical pharmacology and Bioequivalence studies that include:
- PD/PK Studies
- Multi Dose Studies
- Multi Period Studies
- Drug-Food Interaction Studies
- Urinary drug elimination studies
- Cosmetic and safety evaluation studies
- Drug-Drug Interaction Studies
CAPABILITIES
- Phase I to Phase IV studies
- 4 Clinics with a total of 120 beds
- 20 beds ICU with central online monitoring
- Central Nursing station with telemetric monitoring, data recording & data retrieval
- Web linking of ICU with medical experts
- Bio-metric system for retrieval of data.
- Over 15,000 volunteer database.
- ICCU is equipped with ADR monitoring and reporting.
- Recreational area for subjects.
- Adoption of GLP guidelines as per ICH standards.
- More than 100 Validated Methods
- SAS (Ver 8.2), Pharsight WinNonlin (Ver 5.2.1) Software for bio statistics
- QA check at every stage of study.
- Archival for Clinical Documents along with Soft copies.
- Storage facility for biological samples in frozen conditions as required
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