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Removing Barriers to the Production of mRNA-Based Vaccines & Therapeutics

mRNA vaccine is the newest type of vaccine available to the public and has great prospects in terms of speed from research to market. In manufacturing, some barriers observed during Covid can already be lifted up such as (A) a slow transition from research to commercialisation, (B) unequal access to vaccines across countries and (C) inadequate supply of raw materials. Solutions have already been found for (A) a quicker shift from benchwork to commercialisation with a manufacturing process based on repeat-batch production of in vitro transcription (IVT), (B) technology that is small, straightforward to use, modular and transportable to diverse locations and (C) increased number of suppliers for critical raw materials, which are reputable for reliable and predictable deliveries. RNA production with Ntensify™ starts with DNA templates which are first transcribed into RNAs and then purified, ready for encapsulation. In this process, the reaction volume of the in vitro transcription (IVT) is fixed to 20 mL. Large-scale manufacturing occurs by 20 mL increment: i.e. repeat-batch production, with the benefit of an already optimal ratio for reagents (a process co-developed with our partner eTheRNA), which avoids dedicating time to optimisation when entering production. With both high yields and low impurities RNAs, purification can be simplified to a single step. To demonstrate that our approach in 20 mL is successful, several constructs were tested using this process. Their sequence length ranges from 1999 and 4060 ribonucleotides. mRNA reaction yield is on average 5.1 mg/mL. Analysis of the data shows that all batches met the specification limits, where defined.

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EU Chemicals Strategy for Sustainability: implications for the regulation of endocrine disrupting chemicals

The 2020 EU Chemicals Strategy for Sustainability (CSS) has a strong focus on endocrine-disrupting (ED) chemicals, due to perceived concerns over their effects on human health and the environment. The CSS envisages strengthening both the CLP and REACH Regulations with respect to ED chemicals; the CLP Regulation has recently been amended to include additional classification categories for ED, and an ongoing review of REACH will introduce new ED-specific information requirements. These changes will be introduced alongside other measures, which together aim to prevent the development of ED chemicals and remove or restrict ED chemicals currently on the market.

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Building a lab of the future: how to drive business value at the bench

Artificial intelligence and machine learning are bringing digital transformation in labs to the next level, helping to fuel the emergence of “the lab of the future.”
Rather than focusing on data collection, the lab of the future enables data analysis, which in turn helps companies identify important lessons, insights, warnings, and opportunities coded inside scientific data. In the lab, this means greater efficiency and speed-to-market; in the boardroom, it means scientific data is available to support critical decision-making; on a global scale, it positions labs to help address humankind’s most complex and dynamic problems.

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Process characterization of viral vectors: approach in CDMO context

When preparing the clinical supply for product development, viral vectors manufacturers and CDMOs (Contract Development Manufacturing Organisations) have to balance complex requirements. They are expected to move very fast in a highly complex environment, while generating a comprehensive and extensive set of data to submit to Heath Authorities for review. Within the regulations, more and more emphasis is put on Quality by Design (QbD) and process characterization, but the time allocated to these is decreasing. Here, we are discussing two case studies that provide examples on how CDMOs can apply process characterization principles to deliver clinical supply and a robust data set, in due time and of the highest quality.

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