Biologic Outsourcing STREAM
-
Delivering Top Quality Fill Finish Manufacturing
Bringing an innovative parenteral drug product to market requires a fill finish manufacturing partner with the resources and solutions to deliver top quality products and the agility to meet your needs.
-
Bio4C ProcessPad™ Product Overview
5/19/2020
Introducing Bio4C ProcessPad™ Software, part of the BioContinuum™ Platform.
-
Meet The Experts: Part 4 – Applications And Use Of Raman In Bioprocessing
5/1/2023
Watch the fourth and final interview of this 4-part series to learn about Raman applications in bioprocessing from expert Célia Sanchez.
-
A Friendly CDMO Expert: New CEO Outlines AGC Bio's Transformation
3/25/2025
Experience a friendlier, more reliable approach to biopharmaceutical manufacturing with AGC Biologics, your trusted partner for minimizing risks and fostering collaboration.
-
Explore What's Next: Product Characterization
7/17/2019
Newer, high-resolution analytical techniques help answer questions regarding product heterogeneity and drug functions, and help assess for product-related aggregates and impurities.
-
Level Up With Product Characterization
3/12/2021
In the race to bring a new biotherapeutic to market, unexpected obstacles can slow you down or even knock you back a few steps. But with the right information at the right time, and an experienced partner to provide scientific, regulatory, and bioprocessing guidance and support, you can find a smoother, faster path to the finish line.
-
Building A Strong Safety Culture In The Biopharmaceutical Industry
1/25/2025
Explore how fostering a strong safety culture — rooted in accountability, collaboration, and proactive risk management — can drive operational excellence and long-term success in biopharmaceuticals.
-
New Protein A Device Set To Redefine Biomanufacturing
3/25/2025
Discover how the Gore Protein A Membrane Device, in collaboration with AGC Biologics, can revolutionize your manufacturing processes, enhancing efficiency, scalability, and innovation from discovery to GMP-level production.
-
ICH Q7 Good Manufacturing Practice Guide For Active Pharmaceutical Ingredients
6/7/2022
The ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients is the most commonly referenced quality guideline in pharmaceutical product and contains five segments. Watch the video to learn more.
-
MilliporeSigma Capacity Update October 2025: Large Molecule
10/16/2025
Our global facilities are built to guide you when you’re ready to scale; and power your mRNA journey from discovery to global commercialization.