One Focus — Getting It Done. Right.

At ERT, our passion and commitment to transforming our clients’ clinical trial and drug approval efforts is clear. Everything we offer — our expert team, unparalleled service, proven process and leading technology — work together, with one single goal: To deliver the most accurate and regulatory-compliant data that will empower your expert decisions, impacting the success of your clinical trial outcomes. 

Proven Performance. Results That Count.

As the industry leader in cardiac safety drug research, ERT has provided unparalleled scientific and regulatory leadership to biopharmaceutical, Contract Research Organizations (CROs) and medical device companies — around the globe. You can now count on this same skill and demonstrated expertise — spanning our people, process and technology — for a broad cross-section of clinical trial and drug safety efforts, including  ePRO (electronic patient reported outcomes).

ERT is the one experienced partner to turn to for best-in-class solutions and best-in-class advisement, whenever you need to collect and manage clinical data to deliver quality results that support getting your new drugs to market. It’s time to let ERT put our experience to work for you.

Contact us to meet with an ERT associate or inquire about a consultation.