Reduce dsRNA and optimize your IVT with our enhanced enzymes and high‑quality raw materials
WEBINAR
As regulatory expectations intensify, mRNA developers face stricter demands for impurity control, transparent documentation, and consistent raw‑material quality. Enzyme variability and elevated dsRNA reduce mRNA quality, impact safety and translation efficiency, and increase downstream purification burden.
In this insider session, we introduce our enhanced T7 RNA Polymerase and Inorganic Pyrophosphatase (IPP) Emprove® Expert— designed to deliver higher transcription yields, significantly reduced dsRNA formation, and consistent performance across batches. Combined with our high‑quality raw materials portfolio and supported by comprehensive Emprove® Dossiers, these solutions help de‑risk development, strengthen regulatory readiness, and enable reliable, high‑purity mRNA production from early process development through scale‑up.
In this webinar, you will learn:
- Understand why selecting raw materials suitable for pharmaceutical use from the start is essential for reliable, high‑quality mRNA manufacturing.
- Learn why dsRNA formation remains a key challenge in IVT and how new technologies can help reduce manufacturing complexity and downstream burden
- Discover how our enhanced T7 RNA Polymerase Emprove® Expert, and high‑quality raw materials improve transcription efficiency, reduce dsRNA, and deliver consistent performance.
Speaker List

Nelli Erwin
Merck
Strategic Product Manager
Nelli Erwin is a Strategic Product Manager for enzymes and chemicals supporting novel modalities at our company, Darmstadt. With a PhD in Chemical Biology and experience across multiple R&D roles, she combines deep scientific expertise with a strong focus on innovation. Nelli drives high‑quality solutions that help customers advance their processes with confidence and accelerate progress in emerging therapeutic technologies.

Oliver Prince
Merck
Senior Expert pDNA/mRNA/ GLP-1
Oliver Prince, Ph.D., is the Senior Modality Expert for pDNA, mRNA and GLP-1 for manufacturing and process understanding in the Americas. His current function is to connect customers and stakeholders to people, ideas and/or solutions to enable innovation and address unmet needs. His continued success in this space is facilitated by previous experience in science, marketing, strategy and serving patients.
Pharma and biopharma manufacturing
- Solid Formulation Strategies
Duration:1h
Language:English
Session 1:Thu, May 28, 2026 4:00 PM CEST
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