Capabilities | Advanced Manufacturing
Scale without borders
Prototype anywhere, scale everywhere. Ascential’s contract manufacturing network keeps your innovative device compliant, consistent, and in motion worldwide.
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Advanced manufacturing.
Built to spec globally.
Our harmonized, FDA/ISO-certified facilities operate under unified quality systems to ensure the same precision and compliance, regardless of where you build.
Complex Manufacturing
Ensure every instrument is built, tested, and documented to the same standard, regardless of volume or manufacturing location.
Design for Manufacturing
We ensure designs can be built repeatedly, compliantly, and at volume, without sacrificing performance or quality.
Clean Room Manufacturing
Protect your product integrity with scalable clean-room production designed for sterility, precision, and compliance.
Design Transfer
Through detailed evaluation, process development, assembly line setup, training, pilot builds, and validation, we ensure every product is ready for efficient, repeatable production.
Test & Inspection
We integrate test and inspection into the manufacturing workflow to catch issues early, verify performance against requirements, and generate the needed documentation rigor.
Asceptic Manufacturing
We deliver reliable, large-scale production of sterile, high-quality life science instruments and consumables through its aseptic manufacturing processes.
Commercializing a breakthrough in rapid AST
Reducing phenotypic AST time from days to hours demanded both precision and speed. Discover how we transformed a complex prototype into a high-performing, fully compliant commercial system.
Redesigning an A/pH sensor manufacturing process
Learn how Ascential helped a leading dialysis innovator move from slow, manual assembly to a fully automated production line, ultimately boosting throughput by 40% and cutting costs 11-fold.
Frequently Asked Questions
Get answers to common questions about our advanced manufacturing capabilities.
Ascential integrates engineering, automation, and regulatory expertise within a harmonized FDA/ISO-certified network. This unified system ensures your device can be prototyped, scaled, and manufactured globally with consistent quality and full compliance.
Yes. We support every stage of your product lifecycle — from small-batch prototyping to validated, large-scale manufacturing — using the same quality systems and process controls across all facilities.
Every Ascential site operates under unified FDA/ISO-certified quality systems with shared documentation, process validation, and traceability standards. Your product meets the same rigorous criteria, regardless of where it’s built.
Absolutely. Our experts manage the entire transfer process, from planning and equipment qualification to process revalidation, minimizing downtime and maintaining product integrity during relocation.
We maintain scalable clean-room environments compliant with FDA and ISO 14644 standards, supporting assembly and packaging of sterile or contamination-sensitive medical devices and diagnostics.
We design and integrate customized automation solutions that increase precision, repeatability, and throughput while maintaining compliance with medical device manufacturing regulations.
Quality is built into every process. We follow ISO 13485 and FDA design control standards, conduct internal audits, and maintain complete traceability throughout the development and manufacturing processes.
Build smarter. Build momentum.
Let’s explore how Ascential can fit into your process and turn your advanced device concept into scalable, market-ready products.
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