Articles, App Notes, Case Studies, & White Papers
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Staying Flexible In Biomanufacturing
The concept of optionality is key to staying flexible in biomanufacturing by keeping your options open and having multiple pathways to take while navigating through this highly uncertain environment.
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Elevating mRNA Manufacturing Toward GMP-Readiness
8/27/2025
The mRNA Technology Transfer Program empowers LMICs with scalable vaccine production. Learn about a partnership that drives innovation in mRNA and sets a global blueprint for equitable health access.
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UniVessel Single Use Bioreactor For CHO Fed-Batch Cultures
7/9/2019
How single use (SU) bioreactors reduce turn-around time and labor required for cleaning and autoclaving traditional glass vessels and minimize associated costs for maintenance and repair.
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Why Invest In Emerging Markets Now
10/10/2018
Unexplored and emerging markets are an attractive prospect for biopharma companies looking to expand. But when it comes to ensuring success, what’s the wisest way to invest?
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The Value Of Peptones For Enhancing Biopharmaceutical Productivity
11/18/2024
Peptones, versatile media additives derived from various sources, offer numerous benefits for biopharmaceutical production.
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Analytics And Bioassays Can Safely Fast-Track mRNA-LNP Drug Development
2/23/2023
One main mRNA technology challenge is the formulation of delivery systems like lipid nanoparticles (LNPs). Learn about evading impurities in lipids, the future of mRNA-based genomic medicines, and more.
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Vaccine Clinical Trials Global Landscape Whitepaper (2024)
12/5/2024
The global vaccine trial landscape is undergoing rapid evolution, driven by technological innovations, emerging health threats, and regulatory shifts.
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Five Essentials For Accurate Oligonucleotide Chemistry
3/4/2024
Explore five key areas in oligonucleotide chemistry where improvements will have a huge influence on your synthesis quality.
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Clinical Development Strategies For Western Biotech Companies In China
9/22/2022
Delve into how China is now more aligned with international standards, enabling biotech firms to streamline processes and timelines, which has significantly recharged biotech innovation.
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Regulatory Expertise And CMC Document Preparation To Support mRNA-Based Therapeutic Development
10/7/2024
Explore the regulatory requirements for mRNA drug substances and products, the importance of phase-appropriate quality, and insights on creating CMC documentation to ensure compliance.