How do we achieve standardization in single-use design—without limiting customization?

This webinar summary explores The Forge, a free, web-based tool that streamlines single-use assembly design, verification, and procurement in minutes.

Read the transcript summary to learn more.

Missed our live webinar? Watch the recording now and discover how The Forge is transforming Single-Use System (SUS) design for biopharma manufacturers. Learn how our cutting-edge rules-based verification, neutral taxonomy, and real-time component comparison can help streamline your design process, ensure standardization, and accelerate time-to-market.

Traditional drafting in bioprocessing often involves repetitive cycles of drawing, revising, and reworking designs, which slows progress and strains resources. Much like a restaurant kitchen that thrives on standardized ingredients and processes, single-use system design benefits from a unified, streamlined approach. Learn how advanced tools and workflows can transform drafting into a faster, more accurate, and collaborative process.

Single-use systems bring flexibility to bioprocessing, but managing complex designs, diverse suppliers, and regulatory standards can be challenging. The Forge by Vulcan Bioworks is designed to address these needs, providing vendor-neutral compatibility, real-time verification, and streamlined workflows that make single-use system design more efficient and reliable. Explore how The Forge simplifies each step, from configuration to procurement, helping teams deliver high-quality, compliant designs with ease.

Designing single-use systems in bioprocessing comes with unique challenges—from managing complex procurement processes to ensuring quality and compliance across components. These obstacles can create inefficiencies, add costs, and slow down project timelines. Our latest blog explores the top five pain points in single-use system design and reveals how The Forge by Vulcan Bioworks is built to tackle each one. Learn how The Forge’s vendor-neutral compatibility, rules-based verification, and streamlined workflows are making it easier to design, standardize, and scale reliable systems that meet today’s bioprocessing demands.