Integrated Resource is a nimble and efficient CRO designed to work with small, mid-sized, virtual bio-pharmaceutical and medical device companies.

 

We provide comprehensive solutions for End to End Clinical Trial Management helping our clients to effectively reduce the time and cost for clinical development.

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IRI is a full service CRO with combination of efficient clinical trial management, comprehensive regulatory consulting and innovative technologies to create a customized approach which ensures ease of execution and cost effective solutions for our clients across the world.

 

Experts at IRI cumulatively delivers the best in class services with 30+ years of experience to ensure rapid and accurate clinical trial results for Bio Analytical & Bio Equivalence as well as Phase I-IV clinical research support in the industry.

 

IRI CRO’s integrated and full service portfolio include the following:

 

• Advanced Central Project Management

• Bio Availability & Bio Equivalence

• Bio-Statistic Solutions

• CDM Expertise 

• Clinical Operations

• Clinical Supplies Management

• Integrated Interactive Response Technology

• Medical Writing and Regulatory Services

• Clinical Resource Simulation Services (Site & Resources Management)

• Clinical Laboratory Services

• Pharmacovigilance

 

Vast experience of the IRI CRO’s Clinical scientific and regulatory experts who are involved in end to end project life cycle provides a great confidence to sponsors for thorough execution and precisely focused for maximum results.