
ABOUT SAMSUNG BIOLOGICS
Samsung Biologics is a full-service provider offering development and cGMP manufacturing services. We deliver a broad range of services from development and manufacturing to fill and finish, covering both clinical molecules and commercial products. Established in April 2011, Samsung Biologics will transform the global healthcare industry over the next decade through our quality, technology and innovation. Our facilities are custom designed for monoclonal & recombinant production with maximum flexibility. Our one-stop services include cell line generation, process and analytical method development, analytical services (characterization, comparability, IPC, lot release & stability), and clinical and commercial bulk cGMP manufacturing of drug substance and drug product. We also provide quality assurance and quality control services, as well as worldwide regulatory compliance standards & support for our customers. We are centrally located in the heart of Asia, within 20 minutes of Incheon International Airport.
CONTACT INFORMATION
Samsung Biologics
300 Songdo Bio Way, Yeonsu-gu
Incheon, 21987
KOREA, REPUBLIC OF
Phone: +82 32 455 3114
Contact: Jinyong Kim
BROCHURES
- Trusted End-To-End CDMO Partner For Your Journey
- Capacity To Secure Your Success
- Take The Right Step To Advance Your Molecule
- CRO Testing Services - Expedite Your Success
- Super Plant 4
- Plant 5 - Dream Plant: Within Your Reach. Built For Your Success.
- Why Samsung Biologics?
- Samsung Biologics: A CDMO Delivering Innovation And Capacity
- Aseptic Fill/Finish Service
- The Power Of One: mRNA Services
- The Choice For Your Next Dual-Specificity Therapeutics: S-DUAL™
- Ensure Success From An Early Stage: DEVELOPICK™
FEATURED ARTICLES
- Addressing And Adapting To Evolving mRNA Market Trends
- β-Glucan As A Process-Related Impurity In Biopharmaceuticals
- Monoclonal Antibody Manufacturing: Build Or Outsource?
- Biopharma Tech Transfer: Facility Fit And Process Gap Assessments
- Choose A CDMO Partner That Integrates Market Intelligence For Aseptic Fill And Finish
- Critical Success Factors For Cell Line Development
- Beyond COVID-19: How Localization Strengthens Supply Chains
- The Challenges Of Biopharmaceutical Quality
- Ensuring A Successful Technology Transfer
- Plan Your CDMO Search On A Foundation For Long-Term Success
- Overcome Data Integrity Challenges In Biopharma Production
- Embracing Necessary Digital Transformation In Biomanufacturing
- Setting The Right Goals: Go Digital, Not Paperless
- Ensuring Stability And Safety In Aseptic Fill/Finish Manufacturing
- Considerations For Successful Upstream Manufacturing Process Scale-Up
- Implementing A More Robust Post-Pandemic Supply Chain
- CDMO Expertise Accelerates Biologics Development, Manufacturing
- Dedicated To Digitalization
- It Depends: The Real Answer To The Single-Use Or Stainless-Steel Question
- Advantages Of A CDMO With Internal Biosafety Testing Capabilities
WEBINARS
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Discover key considerations and challenges in implementing N-1 perfusion technology, as well as the impact of continuous technology on tech transfer and process scale-up.
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This presentation addresses keys to outsourced drug production, including the importance of seeking the right partnerships to help overcome the challenges associated with secure commercial product supply.
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Where reducing time to market can determine a key factor for a successful business, selecting the right pathway from the start is critical to prevent any future risks. Learn about what to consider in selecting the best cell line to accelerate speed to market.
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Unprecedented times provide opportunities to advance innovative technology, establish a robust business contingency plan, and reduce lead time to drug delivery.
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With ongoing development efforts seeing infinite possibilities for cancers, autoimmune diseases, and genetic diseases, how should the industry apply this early victory into successful mRNA-based therapeutics and vaccines?
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This webinar describes the acceleration of tech transfer to enable kickoff to vial thaw for antibody manufacture within three months for a clinical program and five months for process qualification.
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How can you get to IND faster through an accelerated and high-performance proprietary cell line? Learn about a 3-month cell line development timeline and a high-quality cell line with outstanding productivity.
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Here we present process development and characterization strategies required to support commercial scale manufacture of antibody therapeutics.
VIDEOS
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We are determined and resolute in our purpose: to be always dynamic, always responsible, and always innovative. It's in our DNA and it’s a part of who we are.
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Samsung Biologics proudly presents the official launch of their proprietary cell line, S-CHOice, a high-performing technology to start your successful therapeutics development journey. We can now offer our clients even more promising options in bringing their molecule faster and better to the market with world-class client satisfaction.
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Samsung Biologics’ vision is to enrich human life with technology and innovation. By continuously innovating our people, process, and portfolio, we will fulfill our mission to become the most trusted partner to our clients working together to achieve "Better Life" for humanity through biomedicines.
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Using our expertise and innovation, we can help you maximize your opportunity to get your molecule to market and patients, faster and better.