42

Compliance Considerations in Medical/Commercial Collaborations

/in , , , , , , , /by

Objectives:

In this webinar, we explore two scenarios that can open Medical Affairs up to censure. Scenario one explores participation of commercial team members in Medical Advisory Boards and scenario two looks at the implications of a commercial team member requesting a medical team member to participate in a thought leader meeting.

By participating in this eCademy Webinar, attendees will be better able to:

  • • Deep dive into regulatory and other guidance on medical/commercial collaborations
  • • Explore latest updates to laws/regulations governing compliance
  • • Learn best practices & key considerations when conducting Medical Advisory Boards
  • • Explore common compliance risks and approaches to mitigate risk and safeguard credibility in scientific exchange

Access Options

43

Digital Opinion Leaders: A Challenging Role in a Changing Environment

/in , , , , , , , /by

Objectives:

After attending this eCademy Webinar, participants will be better able to:

  • • Harmonize understanding of who a DOL is and the milestones to be considered in the implementation of a DOL initiative
  • • Build a well-defined road map to implement a DOL engagement initiative at a local level

Access Options

45

Real World Data: Unlocking Valuable Insights Throughout the Lifecycle

/in , , , , , , , /by

Objectives:

Real world data (RWD), when captured and analyzed, produces the Real-World Evidence (RWE) that underpins the economic case for innovative medicines. Furthermore, RWD can inform the understanding of disease, help identify new therapeutic intervention points, and improve the efficiency of research and development (R&D), especially clinical trials. Unlocking the potential of any promising tool like RWD is not free from challenge and its full potential has yet to be realized. This Webinar aims to provide practical insight into the challenges surrounding RWD and RWE generation with interactive conversation on how individual companies are approaching these challenges.

By participating in this Webinar and/or the subsequent workshop at the MAPS EMEA 2018 Annual Meeting, attendees will be better able to:

  • • Understand the full spectrum of challenges around the use & integration of RWD & RWE including data availability, reliability, quality of data sources, the cost of data acquisition and integration, and acceptance by key stakeholders
  • • Realize the full opportunity of RWE throughout the product life-cycle supporting all cases from clinical research, pre-regulatory approval and post-approval.
  • • Understand the limitations of RWE, including patient confidentiality, data quality and accessibility, and how they can be overcome
  • • Use this evidence effectively and within frameworks defined by regulators at a country or regional level

Access Options

47

Navigating Career Transitions: How to Maximize Your Impact – Without the Burnout

/in , , , , , , , , , /by

Objectives:

Transitioning into new roles can prove a real test for even the most senior of executives. Up to 40% of new leaders fail, leave or burn out within the first 18 months. Painful and costly for all involved!

This webinar looks at how to navigate the “rollercoaster” of starting a new role, accelerating your career transition and building confidence early on.

Learning Objectives:

We explore during this Webinar how you can successfully navigate your next career transition:

  • • Explore the pitfalls of career transitions, and how to overcome them
  • • Look at the key foundations required to make a successful career transition
  • • Hear real-life stories, and learn actionable tips, from others who have navigated complex career transitions
  • • Explore why health & wellbeing should be a priority on your transition agenda

 

Access Options

52

Patient Centric Real World Data & Evidence Generation

/in , , , , , , , , /by

Objectives:

Making the best possible choices about health care requires the best possible evidence upon which to base these important decisions. High quality evidence comes from many sources including real world data (RWD). The sources of RWD are numerous including electronic health records, claims and billing data, product and disease registries and patient-reported data.

Analysis of RWD leads to clinical evidence known as real world evidence (RWE) regarding the usage and risks and benefits of a therapy. Under the right conditions, RWD and the RWE that follows may be used to support regulatory decisions and contribute to the knowledge of a drug or therapy. RWE may help to support improved decision-making about health and health care.

After completing this Webinar, participants will be able to:
•List the sources of real world data (RWD),
•Understand how real world evidence (RWE) can help to support a regulatory decision,
•Recognize when in the product life cycle RWD/RWE may be useful,
•Utilize a patient-centric framework to develop a RWD/RWE generation plan.

Access Options

Connect with Us

602 Park Point Drive, Suite 225, Golden, CO 80401 – +1 303.495.2073

© 2024 Medical Affairs Professional Society (MAPS). All Rights Reserved Worldwide.

Subscribe to MAPS event and resource updates
MAPS Program Support Services
Policies and Positions