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Everything you need to know about stability CDMOs

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Hosted by StabilityHub, this free webinar explores the what, why, where, when, and how’s of Stability CDMOs.

In an industry where timelines are tight, regulatory expectations are growing, and products are becoming increasingly complex, understanding how to effectively partner with a Stability CDMO has never been more important. Stability functions are often the critical path in development and commercial programmes, yet they demand significant expertise, infrastructure, and strategic planning. This webinar is designed to demystify the role of Stability CDMOs, explain when and why organisations rely on them, and provide practical guidance for teams seeking to optimise their stability operations through outsourced partnerships.

Date: January 22, 2026
Time: 17:00 (IST) | 18:00 (CET) | 12:00 (EDT)
Location: Online (Hosted by StabilityHub)

Managing stability programs in today’s life science landscape is complex. With evolving global regulations, increasingly specialised product profiles, and rising expectations around compliance and data integrity, many life science organisations are turning to a Stability CDMO to strengthen their operations. Whether you’re launching a new product, scaling rapidly, planning for contingencies, or addressing specialised needs, chances are you’ll consider partnering with a Contract Development and Manufacturing Organization (CDMO) at some point.

This free webinar, hosted by StabilityHub, brings together industry experts to break down everything you need to know about working with a Stability CDMO. Designed for professionals in pharmaceutical, biopharmaceutical, and advanced therapy development, it offers a practical, structured deep dive into the what, why, where, when, and how of outsourcing stability storage, testing, and program management. Viewers will gain clear, actionable guidance on how Stability CDMOs can enhance operational efficiency, support regulatory compliance, and help organisations adapt to increasing market and regulatory pressures.

What you’ll learn about working with stability CDMOs

Stability programs sit at the heart of product development and regulatory submission. But not every organisation has the internal capacity, infrastructure, or specialist expertise to manage the full lifecycle, from long-term ICH storage to specialised conditions, method development, testing, and contingency planning. That’s where a Stability CDMO becomes an essential partner.

During this webinar, you’ll gain insights into:

  • What a Stability CDMO actually does
    From stability storage and testing to method development, iso-conversion modelling, forced degradation studies, and emergency backup space, the session breaks down the full scope of services offered by a dedicated Stability CDMO and how they integrate into your end‑to‑end development workflow.
  • Why companies outsource stability services
    Learn the core drivers from operational efficiency, compliance assurance, risk mitigation, reduced capital expenditure, and access to specialist facilities and expertise.
  • Where a Stability CDMO fits in your program
    Understand how outsourced stability functions can complement in‑house teams, support global operations, and provide resilience during inspections, expansions, or product launches.
  • How to choose the right Stability CDMO
    Explore key decision-making criteria including regulatory track record, capacity, environmental mapping, data integrity controls, and service flexibility.
  • Real-world examples of successful Stability CDMO partnerships
    Case studies highlighting improved efficiency, reduced risk, and enhanced regulatory readiness.
  • Live audience Q&A
    A panel of SMEs answering questions on selecting, managing, and maximising value from your Stability CDMO relationship.

Stability CDMO webinar panellists

  • Walter Routh, Founder of Sagana Consulting and Associate Editor at StabilityHub. Walter brings decades of stability science expertise and provides technical insight into program strategy and risk management.
  • John O’Neill, Founder of the Pharmaceutical Discussion Group and Editor at StabilityHub. John is a leading voice in pharmaceutical stability, offering practical guidance and industry-wide perspective.
  • Aideen Glynn, Quality Manager at Q1 Scientific. Aideen brings over 18 years’ experience in pharmaceutical quality systems and stability program management. She leads Q1 Scientific’s compliance and quality initiatives and has extensive insight into how regulatory changes influence day-to-day stability operations.

Watch ‘Everything you need to know about stability CDMOs’ online

Join StabilityHub and an expert panel for this comprehensive session and gain the insights you need to confidently evaluate, engage, and collaborate with a Stability CDMO.

This webinar is free to view online and ideal for Quality, Regulatory, R&D, CMC, Stability, and Operations professionals across the life sciences.

If you enjoyed this webinar, you might also like our webinar on the ICH Q1 Draft Guidelines.