Sanley Clinical Research offers Clinical Research Training courses to young budding Students /Research Scholars / graduates / freshers willing to explore their opportunities in the field of Clinical Research.

• Good Clinical Practice (GCP) Training: Specialized training to ensure compliance with international standards of ICH-GCP for the design, conduct, monitoring, auditing, recording, analyzing, and reporting of clinical trials.

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• Regulatory Compliance Training 

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• ​Clinical Trial Management Training​​​​​​

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• Clinical Research Coordinator (CRC) Training: Training programs for individuals responsible for coordinating various aspects of clinical trials, including patient recruitment, data collection, and regulatory compliance.

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• Site Management Organization (SMO) Training: Training for personnel involved in managing clinical trial sites, including site selection, training, Monitoring, Auditing and oversight.

 

• Customized Training Solutions: Tailored training programs to meet the specific needs of pharmaceutical companies, contract research organizations (CROs), academic institutions, and healthcare professionals and freshers.