What does the BPT measure for pharmaceutical applications?
It characterizes bubble-point and pressure-hold integrity of filters and membranes, giving pharmaceutical teams quantitative data for media design, supplier qualification and lot acceptance.
EXPERIENCE THE Most Advanced Bubble Point Tester
M19 Bubble Point Tester (BPT) for pharmaceutical — AI-based, ultra-high-precision testing. Standards: ASTM F316, ISO 4003.
Model: BPT · Industry: Pharma
Technology principle
The M19 Bubble Point Tester (BPT) measures bubble-point and pressure-hold integrity of filters and membranes for materials used across GMP pharmaceutical manufacturing and QC. Configured for GMP compliance, electronic records and pharmacopoeial / ASTM-aligned methods, it delivers repeatable, audit-ready data so pharmaceutical teams can qualify media, accelerate development and defend specification decisions. Referenced to ASTM F316, ISO 4003, the platform combines precise hardware control with electronic records suitable for regulated and industrial quality systems.
Applications
- Filter cartridge bubble point
- Membrane lot acceptance
- In-process integrity
- Incoming QC
Key capabilities
- Lightweight, compact and ergonomically engineered, the M19 Bubble Point Tester (BPT) pairs a 15" capacitive touchscreen with enhanced pressure- and flow-control hardware, so operators run a full pharmaceutical test sequence with minimal training and shorter cycle times. Available in aluminum or stainless-steel variants, it ships with real-time remote support, USB connectivity and remote-control automation. Domestic manufacturing in India and the USA keeps maintenance cost and downtime low, and a 2-year extended warranty is available.
- Modern, low-training user interface
- Lightweight and portable chassis
- IP65 rated · GAMP 5 compliant
- Three secure user levels — Operator, Supervisor and Administrator
- Versatile connectivity — USB, Ethernet and Wireless LAN
- Flexible reporting — built-in thermal printer or network / PDF / CSV export
Technical specifications
| Specification | Value |
|---|---|
| Principle | Liquid displacement / first bubble point |
| Pore size | 0.1–200 µm |
| Pressure | 0–100 psi (0–7 bar) |
| Accuracy | ±0.01% F.S. |
Standards compliance
- ASTM F316
- ISO 4003
Frequently asked questions
Which standards apply in pharmaceutical workflows?
Typical references include ASTM F316, ISO 4003. Method templates can be aligned to your internal SOP and customer specifications.
How does the software support audits and quality systems?
Electronic signatures, tamper-proof audit trails, role-based access and PDF/CSV export support regulated and industrial quality workflows, including LIMS hand-off.
Can the instrument be customised for our materials?
Yes — sample holders, pressure/flow ranges and report templates can be configured for pharmaceutical-specific media and acceptance criteria.
What are the advantages of indigenous manufacturing?
Make-in-India / USA build delivers faster service, spare-parts availability, lower cost of ownership and easier customisation — with extended warranty options.
How do we get started?
Book a demo with your sample set, download the brochure, or request a quote for an industry-configured system with IQ/OQ documentation support.