Near-term strategies for biotech drug developers facing shifting healthcare dynamics

A dynamic convergence of economic, legislative, scientific, and technological influences is molding the future of the healthcare industry – with implications for biotech companies. Healthcare environments are becoming increasingly complex as drug developers increasingly make the transition to next-generation therapeutics, driving demand for clinical innovation. Against this backdrop, the industry continues to pioneer new approaches to engaging with patients, clinical trial teams, and healthcare providers. During a recent panel discussion, Goldman Sachs and Parexel shared perspectives on emerging trends and high-level developments to help biotechs plan their short- and near-term strategies.

Read the full article

1f19cd397a348ae134fbb8b153b1f4f6.jpg

Get more insights from our recent panel discussion with Goldman Sachs, entitled “Decoding Healthcare’s Future: A comprehensive analysis of investment, clinical research and regulatory dynamics.”

Watch the full video

The views and opinions expressed by the authors are their own and are for informational purposes only. They do not constitute a recommendation by Goldman Sachs, or Parexel, for you to take any action.

Return to Insights Center

Related Insights

Article

Expedited Pathways Comparisons - US EU CHN

Oct 19, 2021

Video

Insights with Goldman Sachs Part 1: Future predictions

Jan 26, 2024

Playbook

Early-phase development strategies for navigating regulatory complexity in the EU

Apr 29, 2024

Video

Overcoming asset transfer challenges during a merger and acquisition (M&A)

Oct 20, 2021

Blog

Studying multiple versions of a cellular or gene therapy product in an early-phase clinical trial

Nov 19, 2021

Article

Three strategies for articulating a coherent product value story

Dec 18, 2021

Article

How emerging biotechs can enter the Chinese market and prosper

Jan 18, 2022

Article

How biotechs can strengthen their value story with advanced analytics

Feb 15, 2022

Playbook

What emerging trends in the FDA’s most coveted designations might tell us

Feb 8, 2024

Webinar

Assessing appropriate use of ECAs in clinical trials

May 28, 2023

Blog

Accelerating Delivery and Patient Access to Rare Disease Treatments – Highlights from World Orphan Drug Congress

May 2, 2024

Blog

Adoption of the ICH Q12 guideline: New Horizons for Efficient Product Supply Chain Management for a Key Global Market

Nov 13, 2023

Related Insights

Article

Expedited Pathways Comparisons - US EU CHN

Oct 19, 2021

Video

Insights with Goldman Sachs Part 1: Future predictions

Jan 26, 2024

Playbook

Early-phase development strategies for navigating regulatory complexity in the EU

Apr 29, 2024

Video

Overcoming asset transfer challenges during a merger and acquisition (M&A)

Oct 20, 2021

Blog

Studying multiple versions of a cellular or gene therapy product in an early-phase clinical trial

Nov 19, 2021

Article

Three strategies for articulating a coherent product value story

Dec 18, 2021

Show more