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On demand

From research mRNA to GMP-grade supply

Scale-up considerations, capping chemistry and analytics for therapeutic mRNA programmes.

Date
Available now
Time
52 min
Format
On-demand webinar
Access
Link sent by email

Live session

Plan the path from bench mRNA to clinical supply

Process sciences specialists outline the transitions between research-grade synthesis and GMP manufacture, including analytics and documentation expectations.

What you’ll learn

  • Choose chemistry

    Compare co-transcriptional and enzymatic capping approaches.

  • Scale cleanly

    Anticipate the changes that scale introduces to purity and yield.

  • Document quality

    Understand the analytics and records a clinical programme requires.

Featured speakers

  • Process sciences team

    mRNA manufacturing

    Takara Bio

Registration

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