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"Just to let you know it was/is a pleasure working with the inVentiv Staff. You have been very helpful to us and I believe have done a great job. Your team has been very patient and flexible with us as we request various changes and updates to programs etc...Thanks for making this collaboration between us and inVentiv easy!"
— Program Phase Statistical Analyst, Large Pharmaceutical Company
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| inVentiv Clinical Expands Operations to Emerging Latin American Region |
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| inVentiv Clinical provides high quality, customized, user-friendly integration of data management and biostatistical expertise to help you efficiently collect, manage and prepare your data for approval. Our systems and process are fully validated and 21 CFR Part 11 compliant. Our staff brings experience from more than 500 studies in all major therapeutic categories, ensuring you get what you need, when you need it. |
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| Our biostatistics and programming services are offered as part of full clinical trial services or as discrete, functional services, including: |
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Study design, including sample size determination |
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Statistical analysis/SAP |
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SAS programming |
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Data integration and CDISC mapping |
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DSMB Support |
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Proprietary randomization tool |
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Support for abstracts and presentations |
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ISS/ISE preparation |
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Paper/electronic submission support for drugs/devices/ biologics |
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Agency interaction |
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Statistical reports |
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Off-Shore Support |
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| inVentiv’s experienced, English-speaking resources in Mumbai and New Delhi, India, provide added time zone coverage, accelerated ramp-up and strong, cost-effective execution for data management, statistics, programming and medical writing projects. You can be assured of an established technology infrastructure and a team of highly trained professionals (ICH, GCP, 21 CFR Part 11). inVentiv has proven strategies for providing time- and cost-efficient solutions. For more information on our Off-Shore Solutions, click here.
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| Download our Biostatistics & Programming Fact Sheet |
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