Medical Affairs

GE Healthcare's Medical Affairs Information for Life Sciences

Medical Affairs

GE Healthcare's Medical Affairs Information for Life Sciences

800-654-0118  
8:00 AM - 5:00 PM ET
professionalservices.medical@ge.com

Option 1: If you are participating in the IDEAS study and need Vizamyl support
Option 2: Report adverse event, product complaint, or request product information and technical information
Option 3: Pricing – Orders – Returns – Sales Specialists
Option 4: Educational grants and investigator-initiated trials information


Or scan QCR code below with a QCR scanner to get in contact with Medical Affairs.


REVISION UPDATED:

Investigator Sponsored Trials Committee (ISTC)

 The ISTC reviews submissions of proposals by independent investigators requesting funding for research protocols using GE Healthcare's products for research purposes.

Types of proposals reviewed:

  • Human Studies
  • FDA-approved drug product uses
  • Unapproved drug product indications

ISTC Contact Information:

Phone: 800-654-0118 option 4

Email: professionalservices.medical@ge.com

Form: Please complete the Medical Information Request Form on this page

Educational Grants

We at GE Healthcare Life Sciences, Pharmaceutical Diagnostics have had to temporarily postpone accepting new educational grant requests in Q1 of 2019. We apologize for any inconvenience this may cause and encourage you to check back and keep in touch with us. We look forward to continuing to support and participate in the medical community's knowledge growth.

Pharmacovigilance

What is an adverse event?

An adverse event is any untoward medical occurrence (resulting in identifiable symptoms or signs) associated with use of a drug product.

Upon learning of an adverse event, 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 800 FDA 1088 (or www.fda.gob/medwatch) should the reporter not wish to contact GE Healthcare.

Product Complaints

What is a product complaint?

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.

Who can report an adverse event or product complaint?

  • Physicians
  • Other healthcare professionals
  • Patients and/or their representatives (including legal counsel)
  • Sales specialists
  • Customer services personnel
  • GE Healthcare employees
  • Customers

You: Upon learning of an adverse event, contact Pharmacovigilance 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 800 FDA 1088 (or www.fda.gov/medwatch) should the reporter not wish to contact GE Healthcare.

FieldBased Medical Directors

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

We collaborate with key experts in the field, providing expertise and resources in support of quality patient care, while obtaining the medical data needed to support GE Healthcare products. We support our customers by:

  • 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
  • Advocating for key customer needs at HQ
  • Supporting research and educational grant opportunities with customers, as appropriate

Disclosures