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» Products & Services » » Medical Affairs » Field Medical Excellence

Enhancing MSL Interactions with Non-US Healthcare Practitioners

ID: 5541


Features:

3 Info Graphics

12 Data Graphics

100 Metrics

6 Narratives


Pages/Slides: 22


Published: 2019


Delivery Format: Online PDF Document


 

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  • STUDY OVERVIEW
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Non-members: Click here to review a complimentary excerpt from "Enhancing MSL Interactions with Non-US Healthcare Practitioners"

STUDY OVERVIEW

As the role of Medical Science Liaisons (MSLs) continues to evolve around the globe, pharmaceutical companies are continuously re-evaluating and updating their guidelines for scientific interactions between MSLs and Healthcare Practitioners (HCPs) in countries and regions outside the United States.

This study presents insights on current MSL practices around HCP interactions outside the US; topics addressed include proactive disease presentations, unsolicited requests on clinical data and off-label uses, and group HCP presentations. There are also questions about MSL re-certification.

Leaders of global or Non-US pharmaceutical field medical teams can use this research to see how their approach to MSL interactions with Non-US HCPs compares with current industry practices for scientific interactions between MSLs and Non-US-based HCPs, including gray areas such as off-label questions and group HCP presentations.


KEY TOPICS

  • Executive Summary: Methodology, Participants, & Key Findings
  • MSL Interaction with Non-US HCPs
  • MSL Involvement in Proactive Disease State Education
  • MSL Engagement with KOLs in Early Development Stage
  • Best Practices for MSL Interactions
  • Recertification of MSLs

KEY METRICS

  • Are your MSLs allowed to speak/present a short overview of general information on standard of care treatment in a proactive disease presentation?
  • If a HCP requests that a MSL leave behind slides from a disease state presentation, are your MSLs allowed to leave the information with the HCP?
  • Upon receiving an unsolicited request, can a MSL present in a group setting clinical data on a product that is not yet approved? If you answered “no,” please indicate why? If you answered "yes," how does your organization/MSL team define a HCP group setting?
  • Upon receiving an unsolicited request, can a MSL present in a group setting off-label clinical information of an approved product? If you answered “no,” please indicate why? If you answered "yes," how does your organization/MSL team define a HCP group setting?
  • During a presentation to a small group of HCPs (i.e. an in-service presentation consistent with label), can your MSLs respond to off-label questions to the group? If you answered “no,” how does your MSL team handle an off-label question in a HCP small-group setting?
  • At what stage of the development of a product do you allow your MSL to do proactive disease state (non-product) education? (Mark all that apply)
  • How early in the development process are your MSLs actively engaging KOLs? (Please select one)
  • How often do your MSLs undergo recertification?
SAMPLE KEY FINDINGS
  • Leaving Disease State Slides if HCP Requests: A majority of participants - 62% - have no restrictions on allowing MSLs to leave behind disease state slides if a HCP requests; the remaining 38% allow it but only if pre-approved or requested.

METHODOLOGY

This study engaged 9 non-US medical affairs leaders from 9 world-class biopharmaceutical companies. Fifty – six percent of the respondents are at the Director level (5); 22% at Head (2), 11% at Lead (1) and 11% at Manager (1).


Industries Profiled:
Pharmaceutical; Biotech; Diagnostic; Health Care; Biopharmaceutical; Clinical Research; Laboratories; Manufacturing; Consumer Products; Medical Device


Companies Profiled:
AbbVie; Stealth Biothreapeutics; Abbott Vascular; Sanofi; Bayer; EMD Serono; Janssen; Astellas; Allergan; Ferring Pharmaceuticals; Sanofi Genzyme; Sandoz; Alkermes; BioMarin; AcelRx

If you purchase Best Practice Database document(s), you will have 30 days from the date of purchase to apply some or all of the cost of the document(s) toward the cost of a Full Access Individual, Pharma, Group or University Membership. Write us at DatabaseTeam@bestpracticesllc.com or call David Guinn at 919-767-9179 if you have any questions.