top of page




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.

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.

End to End Solutions
bottom of page