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Grand Rounds February 2, 2024: Strategies for Improving Public Understanding of FDA and the Products It Regulates…Why Should We Care, and What Might We Do? (Susan C. Winckler, RPh, Esq)

Rethinking Clinical Trials

Winckler, RPh, Esq Chief Executive Officer Reagan-Udall Foundation for the FDA Slides Keywords U.S. Food and Drug Administration, FDA, Misinformation, Communication, Health Information Key Points U.S. Consumers trust policy – and the scientific evidence on which it is based – if communicated to them properly.

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Pharma brands must ‘up the ante’ in their digital presence

pharmaphorum

This year as a nation – and globally – we are more aware of our health than ever before. Coupled with national and regional lockdowns, consumers want to minimise face-to-face contact as much as possible. As with Google, use target keywords relevant to your audience. The challenge of compliance.

Branding 102
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Grand Rounds March 24, 2023: From Observational Studies to Pragmatic Clinical Trials: (Almost) A Decade of Research in PCORnet® (Erin Holve, PhD, MPH, MPP; Russell Rothman, MD, MPP; Schuyler Jones, MD; Neha Pagidipati, MD, MPH)

Rethinking Clinical Trials

We have tried to build engagement that helps us work with the CRNs and health systems to engage a broad array of stakeholders for each project we are doing. Are there ways it can work more smoothly, take advantage of technology, have more consumer information that can facilitate these efforts? For now, PCORnet®.has

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What CX Tech Innovations Options Are Ripe for Consideration?

pharmaphorum

The text can then be scanned and analysed for keywords. On the other hand, I have many friends with a medical background, who are very excited by the potential of digital to improve the lives of patients and avidly follow each advance and development in the world of consumer and med tech. The technology is relatively mature now.

Sales 52
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A New, Automated Approach to Patient Identification for Clinical Trials

ACRP blog

Keyword searches, manual reviews, outdated reports, and other time-consuming and expensive methods are commonly used to find eligible candidates for enrollment. For example, 55% of clinical trials are terminated due to failure to meet enrollment targets, 1 and 11% of clinical trial sites never enroll a single patient.