Newsletter | June 27, 2026

06.27.26 -- Focusing On The Big Picture And The Factors Shaping Biopharma In 2026

HOW DO EXPECTATIONS COMPARE TO REALITY?

Greetings! Since I’m sure many of you are returning from this year’s BIO International Convention, it felt fitting to broaden this week’s editorial focus to examine the industry developments, trends, and factors shaping biopharma in 2026.

 

It’s that time of the year when industry outlooks start getting measured against reality. So, I gathered my fellow editors on the podcast to wax on how the year is progressing and discuss the industry’s major developments thus far into 2026. If you’re interested in listening to that full editorial roundtable, click here.

 

In case you missed it, GlobalData’s “May 2026 CDMO Opportunities And Threats Report” is now available, which identifies CDMOs that may be impacted by key events affecting their clients (e.g., acquisitions, licenses, approvals, etc.).

 

While you’re at it, listen to the newest episode of “Better Biopharma,” featuring Noveome Biotherapeutics’ Larry Brown, Sc.D., where we talk about the company’s first-of-its-kind secretome therapy. Brown explains the story behind this novel therapy, the GMP manufacturing process Noveome developed to produce it, and the CMC challenges it faces from a regulatory perspective.

 

Before you go, be sure to check out some selected content from our partners below!

 

Tyler Menichiello                             
Chief Editor, Bioprocess Online


Recipharm brings speed and precision to complex oncology programs, overcoming high-potency challenges, supply constraints, and tight timelines.

 

Emulate delivers a data-driven approach to predicting liver toxicity earlier, helping teams reduce costly failures and shape smarter preclinical strategies.

 

Veeva streamlines stability programs with digital workflows, real-time visibility, and automated reporting, helping teams modernize their approach.

 

Miltenyi Biotec explores how automation is advancing iPSC manufacturing, improving consistency, scalability, and regulatory alignment.

 

Primrose Bio achieves precise, reproducible conjugation on CRM197 by balancing structural constraints, site selection, and scalable expression — discover how.

 

Roche CustomBiotech reveals how a high-performance endonuclease enables precise nucleic acid removal, supports regulatory readiness, and streamlines workflows.

 

Ensorcell examines how early equipment choices quietly dictate development and why rethinking workflows now can unlock measurable gains for the future.


Connect With Bioprocess Online: