BD BBL™ IC-XT Pack Trypticase™ Soy Agar with Lecithin, Polysorbate 80, RODAC™ Snap Lid
BD Sterile Isolator Cleanroom eXtended Temperature (IC-XT) plated media with a validated SAL of 10-6 offer flexibility and sample integrity to meet today's environmental monitoring needs.
BD BBL™ IC-XT Pack Trypticase™ Soy Agar with Lecithin, Polys
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BD BBL™ IC-XT Pack Isolator Cleanroom, eXtended Temperature sterile plated media for EM applications
provide:
STORAGE FLEXIBILITY
• A storage temperature range of 2-25°C provides improved flexibility and resource utilization with a reduced need for refrigeration.
SAMPLE SECURITY
• SNAP LID RODAC™ plates reduce risk during sampling and handling, optimizing sample integrity.
RESOURCE EFFICIENCY
• Maximize batch sizes and reduce incoming QC testing with up to 9 months shelf life.
PRODUCT TRACEABILITY
• 2D barcode labels that meet GS1 standards allow samples to be easily identified and tracked.
OPTIMAL MEDIA APPEARANCE
• A robust sleeve material with desiccant reduces environmental effects on the media.
STERILITY ASSURANCE
A validated SAL of 10-6 minimizes the risk of false positives, protecting your controlled environments.
EASE OF TRANSFER
• Triple-wrapped packaging enables easy transfer and storage while maintaining sterility.
VHP RESISTANCE
• Packaging is validated to withstand Vaporized Hydrogen Peroxide (VHP®) penetration. Additionally, each bag contains a hang hole to allow for improved handling in isolators.
EASE OF OPENING
• Even with isolator gloves, opening and removal from the packaging is simple.
Note: Not all products are available in all geographies, please contact your local BD representative for product details, specs, or ordering information.
Top tips for environmental monitoring of pharmaceutical clean rooms
Environmental monitoring of pharmaceutical clean rooms is crucial to maintaining exceptional hygiene standards and ensuring the safety and efficacy of the final pharmaceutical product.
In this infographic, delivered in partnership with BD, gain practical insights on how to define your environmental control plan and methodology, considerations for regulatory compliance, and explore insights from fellow scientists exploring purchasing considerations for microbial monitoring plates.
Top tips include:
- Viable vs non-viable environmental testing methods
- How to define your environmental control plan and methodology
- Compliance with Food and Drug Administration (FDA) and European Medicines Agency (EMA)
- Key purchasing considerations for microbiological monitoring plates from an independent survey
