Newsletter | November 29, 2023

11.29.23 -- CDMO Engagement Timeline For Gene Therapy

SPONSOR

Webinar: Practical Applications Of ICH E6(R3): What Do We Need To DO?

Join industry experts December 14 as they discuss the strategic, conceptual, and operational implications of the shift toward risk-based monitoring in the ICH E6(R3) draft guidelines and what sponsors and vendor partners should already be doing to thrive in the future of clinical trial management. Click here to learn more.

FEATURED ARTICLES

AI Predictions From The CPHI Annual Report

The CPHI Annual Report 2023 that was released last month includes insights from 250 global pharma companies and predicts that “within 10 years, over 50% of approved drugs will involve AI in their development and/or manufacturing.”

How Prioritizing OpEx Can Raise Sinking Biopharma Valuations

As investment in the life sciences industry decreases, young companies struggle to keep the lights on. Young companies may overcome these challenges by implementing operational excellence (OpEx) early on in drug development rather than waiting until manufacturing start-up.

CDMO Engagement Timeline For Gene Therapy

In ISR’s inaugural Gene Therapy CDMO Benchmarking Report, we asked respondents to identify the stage in which their company would typically engage a CDMO to support their gene therapy manufacturing needs.

INDUSTRY INSIGHTS

The FDA Race And Ethnicity Diversity Plan: How It Affects Clinical Trials

Consider these steps when creating a more inclusive environment and how enrolling participants in clinical trials from underrepresented racial and ethnic populations can make cancer care more equitable.

DIGITAL EDITION

November 2023 Digital Edition

Inside you will find more on:

  • Top Executive Interviews
  • Companies To Watch
  • Hiring Strategies
  • Risk Mitigation

View the digital edition.

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