Formidable barriers to biosimilar adoption have been identified and discussed extensively in the literature. However, studies are lacking to identify actionable strategies for overcoming these barriers, specifically to achieve goals set by the Biologics Price Competition and Innovation Act […]
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Best Practices for Negotiating Payer Contracts As Cost Shifts from the Payer to the Patient
Negotiating the most effective reimbursement rates with payers has always been a challenge for healthcare providers. In 2019, as high deductible health plans continue to rise and patients take on a greater share of the cost, providers are faced with an even greater challenge: How do revenue cycle […]
Data Validity and Regulatory-Grade Real World Evidence
Data validity is the cornerstone of evidence-based medicine. As randomized controlled trials are augmented by real world evidence, data validity has come under question. Are the data sufficiently valid to support a conclusion? In this webinar, our featured speaker will discuss various types of real […]
Creating a Successful Global Value Dossier
A global value dossier presents evidence-based messages and scientific information that demonstrate the value that your new drug brings in meeting unmet needs. To gain market access, your research findings and value must be clearly articulated, evidence-driven and tailored to target audiences to […]
Improving Patient Matching in your EHR: A Case Study
There are ways to improve any EHR system’s patient matching performance without disrupting any core MPI functionality. View this webinar to hear how Northeast Georgia’s HealtheConnection tackled their patient matching problem with a simple, cloud-based technology, and to learn how:MPIs are […]
Common Challenges and Solutions in Analysis and Reporting of PROs in Oncology Clinical Trials
Oncology clinical trials present unique challenges for collecting, analyzing and interpreting patient-reported outcome (PRO) data. Join us as our panel of experts discuss these challenges and outline some solutions to overcome them. You’ll learn:The specific challenges associated with the […]
What you should know about Patient Reported Outcomes Interviewing: Instrument Development & Regulatory Submissions Requirements
On-demand Webinar
The inclusion of patient and caregiver voices is increasingly valued in the process of collecting patient-centered data for regulatory submissions. Interviewing plays a key role in exploring the patient experience and uncovering patients’ preferences and expectations for treatment (e.g., […]
Bringing the Inside Out: Chart abstraction methodologies that integrate physician insights
On-demand Webinar
With growing acknowledgment of the limitations of randomized clinical trials (RCTs), and a corresponding recognition of the discoveries revealed from practice experience, regulators, private and public payers and physicians are increasingly looking towards real-world evidence to inform their […]
Online MS in Applied PharmacoEconomics or Managed Care from the University of Florida
On-demand Webinar
Join us for interactive, informative webinar to help acquaint you with the well-respected Online MS Degree Program in Applied PharmacoEconomics or Managed Care Pharmacy Systems, from the University of Florida. In this 1-hour webinar, we will cover: Program Overview of the Online MS […]
Rise of the Robots: Leveraging Artificial Intelligence For Better, Faster Systematic Reviews
On-demand Webinar
The potential of natural language processing (NLP) and AI-based tools to accelerate screening and data extraction in systematic reviews continues to be a hot topic in evidence-based research. If you are involved in conducting systematic reviews, you’ve probably wondered whether artificial […]
FDA and 21st Century Entrepreneurial Regulation
Pre-Recorded Webinar Entrepreneurial regulation is a philosophy that allows agencies such as the FDA to be both regulator and colleague to the industry. In such an environment, regulators gain the ability to:Develop policies that are an incentive for innovative medicines Advance the […]
Managing Living Literature Reviews
Sponsored by Evidence Partners, this tutorial will take attendees through the process of creating, managing and updating systematic literature reviews using the Distiller suite of literature review tools. Find out more here. (Source: American Medical Writers association) […]
5 Best Practices for Screening & Data Extraction in Systematic Reviews for Evidence Researchers & Medical Communications
So you need to conduct a systematic review for clinical evidence, economic evaluations, or comparative effectiveness, but you aren’t sure that your process is as thorough, efficient, or complete as it should be. How can you make sure you are using the most efficient and up-to-date Best Practices? […]
ISPOR’s New Member 101 Webinar
ISPOR recently hosted a New Member 101 webinar providing an overview of the Society and its many benefits and services. Members can now access the webinar on-demand here. […]
FDAMA 114 Partnership Forum Proceedings
Webinar recorded on July 20, 2016 Provisions passed under Section 114 of the Food and Drug Administration Modernization Act of 1997 (FDAMA Section 114) established an evidentiary standard for promotional dissemination of health care economic data. However, neither regulations nor guidance in […]
