Clinical Operations at IRI CRO involves core aspects of Clinical Trial Management in great alliance with Site Identification, Site Start Up, Clinical Monitoring, Medical Monitoring, Clinical safety & Pharmacovigilance coupled with support services for exceptional customer service. Our Clinical Operations team strives to create highly collaborative Client relationships to deliver fast, successful, and scientifically sound project deliverables. Our Project Managers work internally and with the client to maximize project performance, clinical excellence, data integrity and product safety.

 

At IRI CRO, we offer a seamless execution of the clients’ clinical study program. Our team is highly experienced for your clinical study service requirements related to Bioavailability / Bioequivalence studies, Early Stage and Late Stage Development, Pharmacovigilance & Clinical Safety, Data management, Clinical Supplies Management including Drugs and Ancillaries, Medical Writing, Regulatory Affairs, etc.

 

Our seamless Project Management support helps to ensure hassle free study execution in compliance with GCP standards with the help of comprehensive quality assurance plan, collaborative vendor management activities and pro-grade tools.

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Our Clinical operations team is empowered in a holistic manner with certain value addition to the clients such as grouping clinical study delivery functions into one cohesive, delivery excellence unit

Our solutions remain available to serve the needs of Large scale, Medium Scale and Small Scale Pharmaceuticals, Biotech and Medical device companies in terms of high quality data and study reports delivered on time and to budget.