Manas Clinical Research Pvt. Ltd.

www.manascro.com

Manas Clinical Research Pvt. Ltd. is a Unique Service Provider in Clinical Research. We offer contract services that help global pharmaceuticals to perform Quality Clinical Research. We believe in commitment to quality work within the appropriate timeframe. We have SOP and quality driven system to perform our services. Our team is committed to provide excellent service to our clients. We believe in quality work with transparency with our clients. For us, nothing is more important than service to our clients. Our Team Experience:  Preparing and facing various audits from DCGI, USFDA, AFSAAPS, WHO and ANVISA  Designing protocols for over 500 BE studies including special design multiple dose studies and special population studies  Monitoring, conducting and managing more than 550 BE studies  First in man – Phase I study  Establishment of unit for Phase II trial  Excellent experience in medical writing and translation  Monitoring of Clinical and Bioanalytical Phases of bioequivalence studies Our Services: 1. Monitoring of Clinical Trials 2. Audit of BA/BE and Clinical Trial Sites We offer pre-study CRO audit as well as system audit of CROs: a) Pre-study CRO audit/CRO selection b) Pre-regulatory system audit of CRO and Clinical Trial Sites 3. Project Management of BA/BE studies 4. Medical Writing and Translation 5. Consultancy 6. Training

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Manas Clinical Research Pvt. Ltd. is a Unique Service Provider in Clinical Research. We offer contract services that help global pharmaceuticals to perform Quality Clinical Research. We believe in commitment to quality work within the appropriate timeframe. We have SOP and quality driven system to perform our services. Our team is committed to provide excellent service to our clients. We believe in quality work with transparency with our clients. For us, nothing is more important than service to our clients. Our Team Experience:  Preparing and facing various audits from DCGI, USFDA, AFSAAPS, WHO and ANVISA  Designing protocols for over 500 BE studies including special design multiple dose studies and special population studies  Monitoring, conducting and managing more than 550 BE studies  First in man – Phase I study  Establishment of unit for Phase II trial  Excellent experience in medical writing and translation  Monitoring of Clinical and Bioanalytical Phases of bioequivalence studies Our Services: 1. Monitoring of Clinical Trials 2. Audit of BA/BE and Clinical Trial Sites We offer pre-study CRO audit as well as system audit of CROs: a) Pre-study CRO audit/CRO selection b) Pre-regulatory system audit of CRO and Clinical Trial Sites 3. Project Management of BA/BE studies 4. Medical Writing and Translation 5. Consultancy 6. Training

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Country

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City (Headquarters)

Vadodara

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Employees

1-10

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Founded

2011

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Potential Decision Makers

  • Pharmaceutical Consultant

    Email ****** @****.com
    Phone (***) ****-****

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