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
  Storage facility for biological samples in frozen
    conditions as required

  Please Contact 24X7
   040-23802009 (09.00 AM to 05.30PM),
   Mail Id:

  Please Contact
    040-23802057 (09.00 AM to 05.30PM),
    040-23802044 (24X7),
    Mail Id: