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 trust 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
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 expert
Bio-metric system for retrieval of data.
More than 15,000 volunteer database
Experience of conducting 1000 BA/BE studies
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
