TAS-CORE+ Air Sampler
Microbial Air Sampler

TAS-CORE+ Air Sampler

Advanced microbial air sampler with wireless data transfer and 21 CFR Part 11 compliance.

21 CFR Part 11 & EU Annex 11 Location QR scanning LDAP login
01 — 09
What Sets It Apart

Three things you only get from the manufacturer.

01

Patented real-time agar plate detection

The instrument confirms the plate is present before sampling starts and keeps checking throughout the run — not just at setup. Patent Application No. 202421076066. A run cannot proceed against an empty head, so invalid samples are eliminated rather than discovered at incubation.

02

The sampling point defines its own parameters

A Location QR label is configured centrally and affixed at the sampling point. It carries the location, template, frequency, volume, start delay and step count. The operator scans it, the instrument validates it against synchronised master data and loads the full configuration — so the wrong recipe cannot be run at the wrong location.

03

The enterprise platform is included, not an add-on

TASMS ships as part of the solution: a centralised server, multi-site ready, single source of truth. Fleet status, live runs, trending and reporting are available from day one without a second software purchase or a separate facility monitoring system.

Why Sterexa

Engineered for the audit,
validated for the batch.



Sterexa delivers comprehensive calibration, validation, qualification, and lifecycle support services designed to help regulated industries maintain the highest standards of compliance, contamination control, and operational excellence. Our expert team supports pharmaceutical, biopharmaceutical, healthcare, food, and research facilities throughout every stage of their cleanroom monitoring journey.

01

Patented technology

Real-time agar plate detection mechanism — Patent App. No. 202421076066 — setting a new industry standard in precision sampling.

02

ALCOA+ data integrity

Immutable server-side audit trails, NTP-synchronised timestamps, no-overwrite architecture — inspection-ready at all times.

03

ISO 17025 calibrated

Every unit ships with a traceable calibration certificate. Mass-flow sensors auto-adjust for dish volume, air density, and lid variation.

04

End-to-end support

IQ/OQ/PQ documentation, on-site installation, AMC/CMC contracts, and a Pan India service & distribution network.

05

Integrated software

Proprietary TASMS software with user management, audit trail, dashboard analytics, and backup & restore modules.

06

Full lifecycle coverage

From R&D and manufacturing to calibration, validation, and after-sales — one partner for the complete product lifecycle.

Solutions

From the sampling head
to the audit trail.

Sterexa provides advanced environmental monitoring equipment, sterile consumables, calibration services, and validation expertise designed to help regulated industries maintain the highest standards of quality, compliance, and contamination control.

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Sterexa
About Sterexa

We build the instrument
and the evidence behind it

Sterexa Biopharma LLP is a fully integrated manufacturing company specializing in advanced pharmaceutical and biopharmaceutical equipment, regulatory compliance, validation, and lifecycle support.

21 CFR Part 11

Data Integrity

ISO 14698

Cleanroom Monitoring

IQ / OQ

Equipment Qualification

Sampling Integrity

Errors caught at the head,
not at the incubator.

Most invalid results trace back to a setup mistake nobody noticed until the plates came out. TAS-CORE+ verifies the physical state of the sampling head before and during every run.

Patent Application
202421076066

Real-time agar plate detection mechanism.

01

Agar plate detection

Plate presence confirmed before sampling begins and monitored continuously while the run is in progress.

02

Sampling head detection

The instrument confirms the correct head is fitted and seated, eliminating the most common setup error.

03

Head open and head blockage alarms

Open, blocked or missing-plate conditions raise an alarm and abort the run rather than recording an unusable sample.

04

Abort records are kept, not discarded

Aborted runs are fully logged with their metadata retained, so data integrity holds even when a sample fails.

Traceability

Scan the point.
The run configures itself.

No parameter is typed in at the sampling point, which removes transcription error and shortens the time an operator spends in the cleanroom.

Location QR carries the full configuration

LocationQR ID, Template ID, Frequency, Volume (100–2000 L), Start Delay (0–3600 s) and Step Count (1–6) — configured in the Master module, synchronised to the instruments, printed and affixed at the sampling point.

Validated against master data

The instrument checks every scanned label against synchronised master data and starts only on confirmation. Manual selection remains available as an alternative.

Plate identification with GS1 parsing

QR, Data Matrix and barcode scanning with GS1 Application Identifier parsing, so plate lot and expiry travel with the record.

Batch linked to every sample

A batch or label number is entered at the instrument as the Sample Data Name, then free-text searchable in Sampling Data Trend — essential for batch-record review.

Operator identity

User login with role-based access control, LDAP or local PIN, so every record is attributable to a named person.

TASMS Platform

The whole fleet,
visible at login.

TASMS — Trini Air Sampling & Monitoring System — is a server-based platform that turns a set of instruments into one monitoring programme.

01

Instrument dashboard as the landing page

Fleet status tiles for All, Online, Sampling, Head Errors, Aborts, Offline and Disabled with live counts. Instrument cards are grouped by department and filtered by unit, department, Equipment ID or serial number.

02

Live sampling view

Real-time status of a run in progress, per instrument, straight from the server — a supervisor sees the run as it happens rather than after it.

03

Sample count analytics

Per-instrument counts for Today, This Week, This Month, This Year and All Time, plus result-wise Complete, Abort and Error. Every count row is exportable and printable from the card.

04

Sampling Data Trend

Multi-select Equipment ID, User ID and Location with a start and end date-time range in a single query. Returns total samples, locations, equipment and users, the busiest location and equipment, Complete / Abort / Error totals, a daily trend graph, distribution by equipment, location and user, and a toggle to full table view.

05

Alert and action limit management

Out-of-limit excursions are flagged automatically against configured alert and action limits, with auto-notification on exceedance.

06

Central EM programme management

Frequency, volume and location configuration is managed centrally and synchronised to the instruments, with configuration deployable to multiple units at once.

07

Data segregation by unit and department

Dashboards, counts, trends and reports are restricted to the logged-in user's unit and department. Identically named locations in different departments are counted and displayed separately.

08

Inspection-ready report output

Export to PDF and print in non-editable format. The footer carries application, version, user, generation date-time and Page x of y, so output can go straight into an inspection file.

Published capacity
10,00,000
Sampling records
15,00,000
Audit trail records
50,000
Recipes
50,000
Locations
25,000
Users
Automatic backups daily
Compliance Coverage

Every standard your inspector will ask about.

21 CFR Part 11
Electronic records and signatures — instrument and TASMS
EU GMP Annex 1 (2022)
Contamination control strategy and viable air monitoring
EU GMP Annex 11
Computerised systems
EN 17141:2020 / ISO 14698
Cleanroom biocontamination control
Schedule M (2023) / CDSCO
Indian GMP, with local regulatory support
USP <797> / <1116>
Sterile compounding and environmental monitoring
ALCOA+
Attributable, NTP-contemporaneous, no-overwrite, enduring
GAMP 5 Category 4
Configured software — validation pathway pre-mapped
IT & Integration

Fits the way your IT team already works.

Networked, not docked

Ethernet or Wi-Fi to the TASMS server — records reach the platform as they are produced, with no physical sync step.

LDAP / Active Directory

Centralised, IT-managed authentication rather than a separate user list on each instrument.

NTP time synchronisation

Every timestamp is synchronised to network time, which is what makes the contemporaneous element of ALCOA+ defensible.

SSL/TLS encrypted transfer

All instrument-to-server communication is encrypted in transit.

LIMS, MODA and FMS integration

API and file-based integration handled natively by the platform — no middleware layer to license, validate or maintain.

Electronic signature with justification

E-signature capture includes a reason and comment field, so the record explains itself at review.

Ready for compliance

Strengthen your cleanroom
monitoring confidence.

Whether you need microbial air samplers, cleanroom consumables, TASMS software, calibration, validation, or lifecycle support — Sterexa helps you maintain audit-ready contamination control with dependable technical assistance.