Cytiva Videos
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Recombinant Protein Process Development And Scale-Up
6/26/2025
Discover a resin for recombinant protein purification with a standardized protocol that streamlines workflows from lab to production, which saves time and enhances efficiency across development stages.
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Pre-Use Post Sterilization Integrity Testing (PUPSIT) Overview
6/18/2025
Successfully implementing PUPSIT requires balancing regulatory compliance with operational efficiency. Gain insights into regulations, common challenges, and expert solutions to help streamline your pharmaceutical manufacturing process.
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Biomanufacturing Operator Training And Solutions
5/20/2025
Discover a hands-on biomanufacturing training program that empowers operators with essential skills, boosts efficiency, and supports innovation in the fast-paced biopharma industry.
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White Raven's Accelerated Path To GMP Certification
4/28/2025
CDMO White Raven achieved GMP certification using an innovative aseptic filling solution in just 18 months. Discover how meticulous planning and collaboration set a new industry standard for efficiency.
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Service Solutions Designed To Help You Gain Speed To Clinic And Market
4/28/2025
Discover how speed, cost, and regulatory acceptance impact drug manufacturing, as well as learn about aseptic filling challenges and how innovative services can enhance your efficiency and compliance.
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Pioneers And Visionaries: Cell Line Development And AAV Gene Therapy
4/15/2025
Viral vector-based gene therapies offer hope for treating rare genetic disorders and complex conditions. Discover an advanced AAV producer cell line that is revolutionizing scalable, efficient, and accessible gene therapy production.
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Pioneers And Visionaries Of Nucleic Acid And Nanoparticle-Based Therapeutics
12/12/2024
Explore the future of nucleic acid and nanoparticle-based therapeutics, including mRNA, CRISPR, and gene editing, as experts discuss innovative solutions for complex health challenges.
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A Standardized Gloveless Robotic Isolator
10/16/2024
By eliminating human intervention—the primary risk factor compromising drug sterility and quality—gloveless aseptic processing technology offers manufacturers greater flexibility, safety, and regulatory compliance in their filling operations.
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2024 Biopharma Sustainability Review
9/3/2024
800 biopharma professionals from 18 countries were surveyed to assess the industry's progress on sustainability. Watch to explore the findings from this sustainability review.
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Be A Gain Changer With 2x Throughput
5/4/2024
Highly concentrated antibody drugs hold promise in revolutionizing patient treatment. However, new treatments bring forth new challenges in manufacturing. Engineered to deliver the high throughput capacity of high-value drug products, Cytiva Supor™ Prime filters minimize product loss and waste, guaranteeing optimal yield. Watch to learn more about these innovative filters.