Medical Affairs

We are available to:

• Provide medical information
• Answer clinical questions
• Offer scientific or technical support
• Deliver applications training

Investigator Sponsored Trials Committee (ISTC)

The ISTC reviews submissions of proposals by independent investigators requesting funding for research protocols.

• Human Studies
• FDA-approved drug product uses
• Medical and scientific information about GEHC drug products

ISTC Contact Information:

Phone: 800-654-0118 option 4

Email: medical.affairs@ge.com

GE Healthcare Medical Directors are field-based scientists and researchers.

• Providing in-depth medical expertise
• Providing peer-to-peer interactions
• Providing unbiased medical data and information pursuant to requests from healthcare professionals
• Obtaining feedback and insights from clinicians to share with GE Healthcare
• Supporting research and educational grant opportunities with customers, as appropriate

An adverse event is any untoward medical occurrence (resulting in identifiable symptoms or signs) associated with use of a drug product; whether or not caused by the drug product.

A product complaint is any written, oral or electronic expression or communication of dissatisfaction or alleged deficiencies related to the identity, durability, reliability, quality, strength, purity, safety, effectiveness or performance of a device or product after it is released for distribution.

To report a suspected adverse event or product complaint, contact the Pharmacovigilance - Safety group immediately at 800 654 0118 (option 2, option 1) or GPV.DRUGSAFETY@GE.COM

Adverse events can also be reported directly to the FDA at 1-800-FDA-1088 (or www.fda.gov/medwatch )

Please see the following for more information:

Safe Harbor Privacy Policy

California Declaration of Compliance

Licensing and Collaboration

JB65085US | April 2019