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 ICTA can monitor, collect, and analyze safety data throughout a clinical trial. This includes adverse event (AE) reporting, risk assessment, and compliance with regulatory guidelines. ICTA ensures timely submission of safety reports, conducts signal detection, and implements risk mitigation strategies. 

Go to pharmaco-vigilance at ICTA.

ICTA designs clinical trials by developing protocols, selecting endpoints, and determining sample sizes.  They ensure alignment with regulatory standards, ethical guidelines, and study objectives. Statistical planning, risk management, and operational feasibility will also be taken care of.

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ICTA manages biostatistics by designing statistical plans, calculating sample sizes, and performing data analysis. They ensure compliance with regulatory requirements, validate data integrity, and generate reports for regulatory submissions. The CRO interprets trial results, providing insights to support decision-making and ensure scientifically robust conclusions.

Go to Biostatistics at ICTA.

ICTA can handle medical writing by creating clinical trial protocols, investigator brochures, regulatory submissions, and study reports. They ensure scientific accuracy, regulatory compliance, and clear communication, supporting the company’s drug development and approval processes effectively.

Go to Medical Writing at ICTA.