On-Demand Webinars

Outsourced Pharma Capacity Update: Fill/Finish

Advanced Packaging
Aseptic Manufacturing
CDMO
Drug Product
fill finish
Lyophilization
Pharma Development
Pharma Manufacturing
sterile manufacturing

October 2025

Advancing Sterile Manufacturing Through Integrated Expertise

Alcami participated in Outsourced Pharma’s October 2025 Capacity Update: Fill/Finish event, where Madhu Shaik, Senior Director of Manufacturing Science and Technology, and Isaac Agyemang, Director of Manufacturing, shared insight into Alcami’s global fill-finish capabilities and capacity updates.

This virtual event convened leading CDMOs to discuss capacity, technology, and innovation shaping the final stages of sterile manufacturing. During their session, Madhu and Isaac explored how Alcami’s aseptic filling, lyophilization, and advanced packaging solutions safeguard product integrity and patient safety—while maintaining the flexibility to support biologics, peptides, and small molecule programs across every scale.

Hosted by:

Outsourced Pharma

Featured Speakers

Madhu Shaik
Senior Director, Manufacturing Science and Technology, Alcami

Isaac Agyemang
Director, Manufacturing, Alcami

Together, they bring deep technical expertise and real-world perspective on the processes, technologies, and controls essential to delivering high-quality sterile drug products.

Why Watch
✔️ Concise, expert-led discussion on the latest fill-finish advancements
✔️ Real-time insight into Alcami’s current capacity and project timelines
✔️ Tailored for pharma and biotech teams evaluating CDMOs for sterile manufacturing

📥 Access the Recording Now
Fill out the form to watch instantly and learn how Alcami’s integrated approach ensures precision, sterility, and reliability from development to delivery.

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Summary

What You’ll Learn:

  • Current CDMO capacity and timelines for sterile fill-finish manufacturing

  • How Alcami’s aseptic filling, lyophilization, and advanced packaging capabilities ensure product integrity

  • Best practices for maintaining quality and compliance in sterile manufacturing environments

  • The role of integrated analytical and manufacturing expertise in accelerating drug product release

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