BIOLOGIC OUTSOURCING
Your Digital QC Companion For Sterility Testing
Discover software designed to ensure fully accurate data recording in sterility testing and that complies with 21 CFR Part 11 standards for electronic records and signatures.
Flexible Manufacturing That Fits Your Molecule
Complex molecule manufacturing doesn’t follow an established playbook. See how we combine a thorough understanding of client processes and requirements to generate high-quality biologics
Master Your mRNA Manufacturing
Join pDNA and mRNA specialists as they discuss innovative mRNA manufacturing solutions for your purification challenges, mRNA stability, and overall product quality.
Level Up With Product Characterization
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 s...
Discovering A Unique Multimillion Euro Nanotechnology Facility
Dr. David Rowe, Head of Manufacturing at Nanoform, provides an overview of Nanoform's manufacturing capabilities and introduces a new, state-of-the-art nanotechnology facility.
MilliporeSigma Large Scale Capabilities Tour
A detailed look at MilliporeSigma’s new BioReliance® viral vector manufacturing facility and how we have employed the latest innovations and quality systems to deliver best-in-class gene therapy services.
Microbial Expertise That Scales Globally
Want consistency and control in microbial manufacturing? We combine decades of expertise, advanced automation, and global processes to deliver reliable, scalable fermentation performance.
Delivering Reliability With Single-Use Solutions
What does it take to ensure performance and compliance in GMP manufacturing? We optimize single-use systems across upstream and downstream processes, ensuring they perform reliably under GMP conditions.
MilliporeSigma Bio-Expo Live February 2025: Downstream Bioprocessing
Advancements in single-use technologies are transforming antibody-drug conjugate manufacturing and offering increased flexibility. Examine key data, design considerations, operational benefits, and applications in ADC production.
Automated Bioburden Testing Solution
Automation is transforming microbial quality control labs, boosting productivity, minimizing errors, and ensuring data integrity. Discover how digitalization is driving Pharma 4.0 and reshaping lab workflows.
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.
OPTIMA 7000 Fill Line
Ajinomoto Bio-Pharma Services is a leader in aseptic filling, offering a wide range of capabilities for vials with our OPTIMA 7000 fill line. The OPTIMA VFVM 7000 safely processes various types and classes of biopharmaceutical products in 2 mL to 100 mL sizes.
A Friendly CDMO Expert: New CEO Outlines AGC Bio's Transformation
Experience a friendlier, more reliable approach to biopharmaceutical manufacturing with AGC Biologics, your trusted partner for minimizing risks and fostering collaboration.
West Vantage™ Goes Beyond Contract Manufacturing
Successfully advancing a drug-delivery device to market demands more than technical expertise; it requires coordinated execution, regulatory insight, and the ability to scale without disruption.
GLP And The Impact To Start Up Companies
Good Laboratory Practice is often used in laboratories and is necessary for specific investigations. What does it mean? And how can it help start-up companies? Watch this video to learn more.
The Next-Gen Cell Line Development Platform Fueling Biologics Success
Whether you're navigating the challenges of complex biologics or seeking a faster path to the clinic, this discussion sheds light on how innovation in CLD can be a game-changer for your pipeline.
10 Minutes On Optimizing Upstream Process Development
Gain insight into how UPD ensures scalable and compliant processes, facilitates the efficient development of innovative therapeutics, and contributes to molecule development and production.
Meet The Experts: Part 1 - Process Analytical Technology (PAT)
Watch part 1 of this 4-part interview series to learn about process analytical technology (PAT) from expert Stacy Shollenberger.
New Protein A Device Set To Redefine Biomanufacturing
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.
Your Roadmap For Efficient Processes
Struggling with mRNA integrity? Discover essential strategies to boost stability in mRNA manufacturing with innovative endonuclease-free DTT and Spermidine chemicals.
Integrated Technologies And Glycosylation Tuning In Upstream Bioprocessing
Optimize mAb production with innovative cell culture media and feed designs. Explore integrated technologies, intensified fed-batch approaches, and methods to modulate glycosylation profiles in upstream bioprocessing.
MilliporeSigma Bio-Expo Live 2024: Downstream Bioprocessing
To optimize efficiencies and reduce contamination risks, we’ve developed a proprietary new film technology for our single-use assemblies offering enhanced strength, flexibility and durability for safe, leakage-free fluid containment.
Millipore Sigma Bio-Expo Live June 2025: Downstream Bioprocessing
Learn about the development and advantages of a new affinity ligand platform. It provides versatile, single-step purification for recombinant proteins and virus particles, enhancing yield and purity.
Biotherapy Characterization: Binding Assays
MilliporeSigma Senior Scientist Helen Hsu, Ph.D. describes how, with our custom binding assays, and supported with our comprehensive off-the-shelf Fc gamma receptor binding assays, we can help you optimize your mAb production, from clone development through upstream and d...
Meet The Experts: Part 3 - Chemometrics And Model Building
Watch part 3 of this 4-part interview series to learn about chemometrics and model building from expert Johan Cailletaud.
Annex 1 FAQs: Responding To The 2022 Revision
Viewing the Annex 1 revision as a natural extension of current habits, rather than a burden, allowed for a seamless transition. Since contamination control was already standard, the update simply validated existing excellence.
Explore What's Next: Product Characterization
Newer, high-resolution analytical techniques help answer questions regarding product heterogeneity and drug functions, and help assess for product-related aggregates and impurities.
A Targeted Molecular Method For Sensitive Viral Detection In Just Days
Explore the motivations, scientific breakthroughs, and collaborative efforts that contributed to the development of this innovative testing solution to help drive safer, animal-free biomanufacturing solutions.
Storing Your Banks With Ease And Confidence
Discover a biorepository that will fulfill your need of long-term and short-term storage. You can never be too careful with your cell or virus banks. Explore three global sites that will ensure the safety of your bank.
What's Driving The Future Of Biopharma And Outsourcing Strategies?
Review the rapidly evolving world of complex drug development and the critical factors that drive success for products made using different molecules beyond the traditional antibodies.