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Please note: The ViiV ISS portal will be down for a system upgrade from Wednesday, November 14th from 12:00PM EST to Friday, November 16th 5:00PM EST. Please reach out to ops.visions@viivhealthcare.com for any questions or concerns during this time. We apologize for any inconvenience.

ViiV Healthcare Investigator-Sponsored Research (ISR) Programme

ViiV Healthcare (VH) is an independent, global specialist HIV company established in 2009 with the commitment to deliver innovative new options for the care and treatment of people living with HIV/AIDS. As part of the commitment, we recognize the valuable role that our support of investigator-sponsored research (ISR) plays in fulfilling this mission. An investigator-sponsored study is a research effort where the sponsor of the work is the investigator, healthcare institution, or some form of medical network external to VH and is seeking our support to conduct the work. Depending on the type of research, this support may include any of the following: providing drug product or substance; providing funding; participating in collaboration to develop and conduct a study of mutual scientific and/or clinical interest.

VH only supports ISR that has a legitimate scientific purpose. The decision to support a study proposal is based on the importance of the research objectives to medical science or patient care, the scientific rationale for the proposed methodology, and the ability of the study sponsor to deliver a high-quality ethical study.

VH does not support ISR in order to reward healthcare professionals for using, purchasing, recommending, or prescribing VH products or to persuade them to do so by supporting

VH expects that all concepts are discussed with a VH representative BEFORE being submitted in this portal

This ViiV ISR portal currently includes three sections based on the type of study you are proposing and subsequently tracking. Each type has specific information and review processes which allow VH to optimize our response to your proposal and the tracking of the subsequent study activities.

Types of Requests/Studies

Pure Substance Requests/Studies ISS Requests/Studies Collaborative
Requests/Studies
All Safety Reporting must be conducted as per your study agreement. If you need to report a suspected side effect for a ViiV Healthcare medicine that is not part of your study, please click the following.

Report a side effect

To report a suspected side effect, please use the online reporting form below. This facility is provided under our service agreement with GlaxoSmithKline (GSK), so please choose ‘ViiV Healthcare medicines’ from the drop-down product list on the form. In North America, you can report a side effect via the GSK Response Center at 1-888-825-5249, Monday-Friday, 8am - 8pm ET.

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