Outsourcing STREAM

1. Factors Which Impact mAb Process Scale-Up 9/7/2021

   Thinking about your mAb scale-up processes early on can help avoid common pitfalls. Cytiva’s Fast Trak scientists discuss factors that can influence a successful scale-up outcome.

2. A Dedicated Team To Safely Store Your Cell And Virus Banks 2/27/2023

   The safety of your cell and virus banks must be your top priority. Learn about a team dedicated to the safety of your material along with their related services.

3. Thermo Fisher Scientific North America Single-Use Technologies Capacity Expansion 3/2/2021

   Thermo Fisher Scientific is expanding our single-use manufacturing network globally. Some of the largest investments are taking place at our existing Logan, Utah, and Millersburg, Pennsylvania, sites. We are adding space for clean rooms for the manufacturing and assembly of Thermo Scientific BioProcess Containers and fluid transfer assemblies, investing in 2D and 3D chamber manufacturing equipment, and harmonizing our quality systems and processes.

4. 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.

5. The Journey To Safety Through Viral Clearance 12/1/2022

   Discover a simple yet powerful solution for getting viral clearance studies done safely, thoroughly, efficiently, and on your timelines. Learn how to free your teams and trust your project.

6. Commercial Readiness with Orca Bio's Dan Kirby 9/14/2023

   Orca Bio's Dan Kirby has played a hand in prepping more than a few approved biologic therapeutic candidates for commercialization. Equally important, he knows firsthand what makes or breaks post-approval commercial efforts, having played virtually every role there is to play in drug sales and marketing.

7. How To Improve API Solubility By Salt And Cocrystal Formation 3/4/2025

   Developing new APIs is complex and costly, especially with poor water solubility (BCS class II and IV). Explore techniques like salt and cocrystal formation to enhance solubility and bioavailability.

8. Biopharma Resilience: Bionova Scientific Talks Capacity, Speed, And Agility 10/7/2022

   Bionova Scientific shares how a CDMO can offer biopharma companies the flexible capacity they need to meet the growing needs for medicines today and in the future.

9. Increasing The Reach Of Cell And Gene Therapies 4/29/2021

   The cell and gene therapy industry is rapidly evolving from the perspective of “can we commercialize this class of therapeutics?” to “how do we reach patients who need these therapies?”. However, the promise of these biologics can only be realized if the industry approaches manufacturing parity with monoclonal antibodies. A mixture of innovation and brute-force streamlining is needed to create viable cell and gene therapy templates. In this video, we discuss how upstream process optimization is ripe for innovative approaches.

10. Regulatory And Biosafety Testing Expertise 3/31/2026

    Advancing biologics requires confidence in safety, quality, and compliance. Learn how integrated analytical and biosafety testing, backed by decades of expertise, helps reduce risk.