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"I would like to take the time out as well to commend you and your entire team in achieving this milestone. You all worked tirelessly everyday to ensure that this was a possibility and we could not have done it without you guys executing like you did. While it was not always peaches and cream along the way, you guys worked nonstop to do what had to be done. So congratulations on your superior performance, unending dedication and outstanding accomplishment."
— Clinical Research Scientist,
Large Pharmaceutical Company
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| inVentiv Clinical Expands Operations to Emerging Latin American Region |
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| Having the right Clinical Monitors working with your investigative sites is key to conducting a smooth, efficient study. inVentiv Clinical offers a unique set of solutions to fit your Monitoring needs: |
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Full Clinical Trial Monitoring & Management |
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Functionally Based Monitoring SRGs |
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Contract Staffing for Regional/In-house Monitors |
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| Whether you need full project management and monitoring or simply a team of monitors to work on your study, our flexible platform can deliver exactly the team you need to get results. Our in-house and regional monitors have an average of more than 13 years of experience in clinical site monitoring and maintain a wealth of experience across all phases of development and major therapeutic areas (see chart below). All iCS Monitors undertake mandatory training on our SOPs, with additional training on Sponsor-specific protocols and SOPs before beginning work on any study. |
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| Download our Monitoring Fact Sheet |
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