Stability Test Chamber
ICH Q1A(R2) long-term, intermediate and accelerated storage conditions.
Overview
Built around the pharmacopeia, not the catalogue
Pharmaceutical stability, storage and clean-room protocols leave little room for approximation. ACMAS supplies Weiber environmental and stability chambers built to ICH Q1A(R2) conditions, alongside laminar air flow cabinets, biological safety cabinets and pass boxes for sterile and aseptic areas — each specified against your standard, mapped at set point, and delivered with the documentation your quality team needs for audit.
Equipment used in this application
All products
What pharma facilities order from us
Standards we build to
Compliance is specified in, not bolted on
ICH
Q1A(R2)WHO TRS
953Schedule M /
revised Schedule M21 CFR Part
11EN
12469ISO
14644.1
Calibration certificates traceable to national standards
Mapping reports at your set points
IQ/OQ/PQ documentation for audit readiness
Optional 21 CFR Part 11 audit-trail software
FAQ
Pharmaceutical application questions
Which ICH conditions can Weiber stability chambers hold? +
Standard configurations cover 25 °C/60% RH, 30 °C/65% RH and 40 °C/75% RH
long-term, intermediate and accelerated conditions, plus refrigerated 5 °C ± 3 °C storage on
request.
Do you support 21 CFR Part 11 compliance? +
Yes — audit-trail software with electronic signatures and access levels is
available and can be specified at order stage.
Can clean room equipment be validated for GMP audits? +
Yes. Laminar air flow units, biological safety cabinets and pass boxes come
with calibration certificates and can be mapped and IQ/OQ/PQ documented for GMP audit
readiness.
Send your stability protocol. Get a specification and quote.
Conditions, chamber count and validation scope — drawing and quotation within one working day.