2026 ISPE Aseptic Conference
The 2026 ISPE Aseptic Conference serves as a platform where the newest developments in aseptic processing, robotics, and automation are explored in depth. It addresses the complex challenges associated with sterilizing small-batch aseptic products and accelerating their time-to-market.
The conference will deep-dive into the revised Annex 1’s implications, setting new benchmarks for sterile product manufacturing, Quality Risk Management, Contamination Control Strategy, and compliance for computerized systems.
Key topics at the conference include emerging aseptic technologies such as microbiological and online testing, and case studies showcasing flexible and multi-product facilities’ success stories. Participants can look forward to gaining critical insights into small-scale manufacturing for development and clinical trials, managing high-potency compounds, containment strategies, and ensuring sterility.
Furthermore, attendees will learn how to navigate fill-finish tech transfer challenges, integrate robotics effectively, select optimal primary packing options, and implement aseptic procedures seamlessly. The conference will also provide answers to queries about parenteral production, lyophilization, sterilization processes, and GMP practices.
The aseptic conference offers opportunities to interact with your peers and leaders in the industry in networking and workgroup meetings to help you discover ideas that can give you fresh perspective on your operations. These relationships last a lifetime and bring technical value to your professional life. Join us at the 2026 ISPE Aseptic Conference.
Conference Attendees
Navigate the conference platform via the listed links.
- Agenda: Build your schedule
- Featured Speakers: View all session speakers
- Attendee Roster: View the full list of conference attendees
- Presentation: Presentations received from speakers before the conference who have agreed to make them available are currently posted on the conference platform.
Featured Sessions
Staying on Mission: Keeping Public Health at the Core
Pharmaceutical manufacturing exists for a single, non-negotiable purpose: to reliably deliver safe, effective, and high-quality medicines to patients who depend on them. This presentation begins with a reminder that daily operational decisions translate directly into patient impact. Discussion will include how industry is performing today and what can be done to improve as well as practical recommendations for manufacturing operations, compliance strategies, and communications.
Challenges with Implementing Annex 1 at the Global Level
The presentation explores global challenges implementing revised EU GMP Annex 1, including unclear guidance, differing interpretations, technical capability gaps, and difficulties harmonizing requirements across diverse facilities, equipment, and operational models.
Regulatory Compliance & Quality
The presentation guides pharmaceutical manufacturers through implementing the revised Annex 1. It combines regulatory insights with resilient quality systems for compliance. The session covers a risk-informed roadmap to enhance market readiness and patient safety. This session translates complex requirements into actionable strategies for implementation.
Fireside Chat – Trends and Industry Responses
Panelists will examine emerging trends in aseptic processing, discuss how organizations are responding to evolving expectations under EU GMP Annex 1, and address pressing technical and operational questions raised by the industry. This session provides an opportunity to connect lessons learned with forward-looking perspectives on facility design, contamination control strategies, and manufacturing practices shaping the future of aseptic operations.
Spread the Word on Social Media
Use the hashtag #ISPEAseptic and tag @ISPE in your posts highlighting your conference experience. Plus, follow the official hashtag #ISPEAseptic to stay up to date on activities and events throughout the conference and include it in your social media posts.
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