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Episode 17: The Transformative CL&D Strategies Journey with Todd Amrhein

ACTO

Todd Amrhein Award-winning Director of Global Training, Learning and Development, Marketing, and Sales About Todd Amrhein : Todd is a results-driven, award-winning Director of Global Training, Learning and Development, Marketing, and Sales in the biotechnology and pharmaceutical industry.

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FDA Poised to Make Impact on Underrepresented Populations in Clinical Studies

H1 Blog

This effort seeks to provide the pharmaceutical industry with more accurate representation of patient populations, thereby enhancing the safety and efficacy for prescription drugs and medical devices. Hence, pharmaceutical companies need to start making preparations to ensure compliance with the new requirements.

FDA 59
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Trials, Data, Diversity – H1’s Top 5 Diagnoses (Predictions) for Biotech and Pharma in 2024

H1 Blog

Every year, we take a look at annual predictions to help life sciences, pharmaceutical, and healthcare companies understand larger industry trends and dynamics to prepare for the new year. These forecasts, curated by our own experts and thought leaders, shed light on the changes set to reshape the healthcare and pharmaceutical sectors.

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What Payer Trends Can Tell Us About Medication Adherence

H1 Blog

Strategies for Market Access Teams One thing the healthcare ecosystem lacks in the United States is a system of shareable, actionable healthcare data. How do pharmaceutical companies work with payers? For more information about understanding payer and patient utilization trends, request a demo. The answer is payers and claims.

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Building an Exclusive Strategy with Inclusive HCPs

H1 Blog

Trusted Advisors for Scientific Exchange As pharmaceuticals strive to create medications that are more effective and accessible, it’s essential that they engage HCPs early in order to understand the needs of their target audiences.

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The Trust Fall: Building Successful & Diverse Trials Outside the U.S.

H1 Blog

Predictive analytics has been gaining traction as a powerful tool in pharmaceuticals and biotechnology over the past few years, but its potential has yet to be fully realized when it comes to international clinical trials. Request a demo of Trial Landscape.

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Article EMA Thank You What we expect European regulators to do in December 2023

Agency IQ

Expected Action Description of action Date Eudamed Module: Market Surveillance [E.U.] Completed development of the EUDAMED Market Surveillance module Q4 2023 Designation of E.U. Expected Action Description of action Original Deadline Pharmaceuticals – changes to marketing authorisations (review of EU rules) [E.U.]