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TIDES Asia: Oligonucleotide & Peptide Therapeutics
24-26 Feb, 2027
Grand Nikko Tokyo DaibaTokyo

Current Topics in Peptide Manufacturing and Purification

Gain practical insight into reducing variability, improving purification, strengthening analytics, and building more robust peptide manufacturing strategies.

As peptide therapeutics become more sophisticated, manufacturing and purification challenges are becoming more complex. This workshop is designed to help attendees connect process understanding with real-world execution, offering focused insight into the technical decisions that support stronger control strategies, better product quality, and more reliable scale-up.

About this workshop

This workshop brings together current thinking on peptide manufacturing and purification, with sessions focused on process characterization, quality by design, large-scale purification, and analytical development. Attendees will explore how development knowledge can be translated into more effective control strategies and scalable manufacturing approaches, with practical examples relevant to increasingly complex peptide programs.

Reducing process variability in peptide manufacturing

Learn how process characterization and parameter understanding can support more consistent manufacturing outcomes.

Commercial control strategy design

See how development insights can be translated into robust control strategies that support validation and long-term supply.

Quality by design in complex peptide processes

Explore how QbD principles can be applied to challenging peptide APIs, including N-alkyl-rich molecules produced using LPPS.

Platform thinking for peptide process development

Understand how lessons from individual programs can help shape broader process and development strategies.

Large-scale purification of peptide APIs

Discover how advanced purification approaches such as MCSGP can improve efficiency and support scale.

Analytical methods for peptide development

Review analytical considerations that help support product understanding, process control, and progression toward commercialization.

Industry challenges we’ll address

Reducing variability and improving consistency in peptide manufacturing

Defining critical process parameters and robust operating ranges

Applying QbD effectively to increasingly complex peptide processes

Improving purification strategies for peptide APIs at larger scale

Building analytical approaches that support development and commercialization

Translating process understanding into validation, tech transfer, and reliable long-term manufacturing performance

Who will benefit from this workshop?

  • VP / Head / Director of Peptide Manufacturing
  • VP / Director of Process Chemistry
  • Director of API Development
  • Director of Purification / Downstream Processing
  • Head of CMC
  • Director of Analytical Development
  • Director of Process Development
  • Technical Operations Lead
  • MSAT Lead
  • Peptide Chemistry Scientist / Senior Scientist
  • CDMO / External Manufacturing Lead
  • Program Director, Peptide Therapeutics