Solutions
Industry solutions built around our testing equipment — biopharma, pharmaceutical manufacturing and QC laboratories. We do not sell a catalog of boxes; we sell the documented, defensible result your quality system needs at each stage.
Biopharma / Aseptic Manufacturing
Isolator and RABS glove integrity, sterilizing-filter PUPSIT, single-use bag verification and filled-product CCIT — the integrity program that keeps a sterile process defensible from the barrier system through release.
Pharmaceutical Manufacturing
Line and in-process integrity testing for sterile and non-sterile product lines, with the electronic records that turn a test into a defense at audit.
QC Laboratories
TOC, osmolality and full-method filter integrity testing for pharmaceutical water systems and release testing programs — the instruments and documentation the lab runs on every day.
Frequently Asked Questions
How do you decide which instruments a line actually needs?
We start from the application — what has to be verified, on what, at which stage — and map it to the method set your pharmacopeia requires. The result is a short list of instruments with the acceptance criteria that go with them, not a catalog to wade through.
Do the instruments talk to our quality system?
Yes. Our instruments store electronic records sized for five years or more, with audit trails, and the data leaves over Ethernet, USB and RS485 — the shape your LIMS or quality system expects.
Need a quote or technical advice?
Tell us your application — our U.S. team responds with product selection, documentation and pricing.
Request a Quote