Continuous-batch RNA manufacturing: Coming to a lab near you

Fast-track your RNA therapy without compromising quality.

Partner with specialist RNA CDMO Exothera and access the benefits of Ntensify™ – the world-first continuous-batch RNA production platform developed by sister company Quantoom Biosciences. 

Ntensify™: Game-changing continuous-batch RNA production

Continuous process. Unlimited progress.

With access to leading-edge technology and an expert CDMO partner, you can accelerate the progress of your RNA therapy from the earliest stages of drug development and beyond with confidence. By standardizing and automating our process, we remove scale-up and process development steps, helping you reduce costs and achieve higher quality and yields. 

Dedicated specialists, committed to service

De-risk your decision to transform your RNA manufacturing journey with a committed and experienced team of scientific problem-solvers by your side at every step.

Ultimate flexibility for every phase

Access our gold-standard platform and allow our expert team to guide you as you progress to each critical milestone. With a flexible partnership at flexible prices, we give you the right level of support you need to progress your product through each phase.

Why partner with Exothera for your RNA manufacturing journey?

By harnessing the expertise of Exothera and the power of Ntensify™, we enable you to:

Cut typical clinical production timelines by approximately half when compared to traditional manufacturing processes and reducing overall costs

Bypass time-intensive process development and scale-up activities

Reduce your cost of goods (COGs) by half

Achieve high post-purification yields with consistently high quality

Introducing: Endless opportunities for your RNA therapy

From vaccines to personalized cancer medicines, our scalable platform and technical capabilities enable you to develop and manufacture high-quality nucleic acid-based therapies. 

By harnessing automation for greater efficiencies, Ntensify™ reduces clinical development timelines – enabling you to reach your next milestone with remarkable speed.

Achieve higher yields at consistently higher quality with a solution that limits user handling to mitigate the potential for variability.

From discovery to GMP, our ecosystem of solutions is designed to support you at every stage, whether you require a single batch or continuous large-scale production for large-scale vaccine manufacturing. With kits for R&D in academia, variant screening and GMP production, we support your seamless transition from early-stage development to commercialization.

With access to the team that invented the Nfinity and the expertise of our scientific and regulatory teams to guide you, you can confidently advance your product through the critical milestones on its journey to patients.

Partnering with you to understand your project, our dedicated team works hard to provide tailored solutions and offer the right level of support you need to advance to your critical milestones.

Whether you decide to onboard the technology into your own facility or let us take the reins long-term, we flex with you to give you the right support and capabilities as your product progresses.

We strive to make our offering accessible to companies of all sizes, regardless of your stage in drug development. Early-stage companies can access our ‘fast track’ package for research use, with the option for flexible pricing models. Onboard early and experience the ongoing benefits as your product progresses seamlessly through each milestone with ease.

Ready to get started?

Take the first step in your continuous-batch RNA manufacturing journey and discover where Ntensify™ can take you. 

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About Exothera 

Exothera is a Belgium and US-based CDMO delivering customized process development and GMP manufacturing services for viral vectors (AAV, AV, HSV, LVV, …) and mRNA or saRNA projects. As a Univercells company, Exothera capitalizes on novel manufacturing technologies and best-in-class bioprocessing expertise to provide bespoke process optimization and GMP clinical and commercial production of viral vectors and nucleic acids. 

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