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Sannova through its bilateral clinics has access to little over 1,000 beds. These clinics have been operating under strict GCP environment and have conducted more than 3000 clinical trials successfully with commitment to quality, accuracy and accountability.
- Two dozens of clinics scattered over USA and Canada.
- Experienced clinical staff.
- About 10,000 healthy normal male and female volunteers.
- Spanning over 18 to 50 years of age.
- Multiracial and diversified subject pool.
- Rapid volunteer recruitment.
- Utmost care for volunteer and patient safety.
- If required, access to special volunteer group.
- Protocol preparation.
- Strict adherence to regulatory practices and protocol.
- Independent IRBs.
- Capacity to conduct 2 dozen studies per month.
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Controlled Drug Substances:
Sannova conducts bioanalytical studies for schedule
II, III, IV & V controlled drug substances. |
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Robust Methods for several ther- |
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-apeutic areas. |
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Controlled substance methods |
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(CII-CV). |
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Preclinical and clinical sample an- |
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-alysis. |
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BA/BE studies & PK/TK data ana- |
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-lysis. |
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State of the art equipment. |
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Reports in eCTD format. |
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Access to clinics in USA, Canada& |
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India. |
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Complete project management. |
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Electronic submission services. |
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Strict adherence to GLP. |
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Strict security and confidentiality. |
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Method Development |
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Method Validation |
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Pre clinical & clinical sample ana- |
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-lysis. |
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Report preparation for bioanalyt- |
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-ical studies reporting. |
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Pharmacokinetic & Toxicokinetic |
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Statistics |
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