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Our Clinical Trial & Pharmaceutical Consulting services are designed to mold and adjust to your specific needs, while maintaining a focus on practical solutions and cost effectiveness.Whether it’s needing information and advice regarding the regulatory landscape and operating environment in India, identifying partners for manufacturing, formulation development, licensing, or establishing new operations, Clinovation has the expertise and track-record to help you do it successfully. Built around the expertise of our personnel who offer over 100 years of collective experience, we can help you successfully navigate the dynamic and challenging clinical research environment in India.
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Clean, high-quality data is one of the most critical elements of any clinical trial. Therefore, data management is a core service of Clinovation and a critical part of our overall customer value proposition. Between the full-time dedicated clinical research coordinator we place at the site and our highly skilled project and data management personnel; we ensure that the data coming out of the investigative sites for your study is the highest quality possible. We have the experience, bandwidth and technology necessary for on-time database lock for any study that we take on and the commitment to make it happen.
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Service Provider of a wide range of services which include Site Selection Procedure, Contract Management, Site Set Up, Document Collection and Create Source Document Template.
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Offering you a complete choice of services which include Clinical Research Consultancy, ICH - GCP Training, Training Of Site Staffs and Clinical Research Services.
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