Newsletter | May 3, 2024

05.03.24 -- Looking For Help With Your Pharmaceutical Facility Design Project?

Streamlined Facility Design: A Success Story

Examine how one medium-sized US company's need for a new aseptic compounding and fill/finish facility was addressed with a tailored solution within a challenging timeframe.

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Cencora PharmaLex

cGMP Facilities For Pharmaceutical Manufacturing

ETL facilities provide a suitable cGMP environment for operators to perform sampling or dispensing tasks. With material and personnel airlocks and a downflow booth, each facility operates with a positive pressure to aid in achieving a clean cGMP environment.

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Dec Group

Periodic Cleanroom Monitoring

TSI’s cleanroom facility environmental monitoring products with built-in redundancy provide the confidence you need to reliably monitor critical processes and demonstrate compliance.

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TSI Incorporated

Pharmaceutical Cleanroom Environmental Contamination Monitoring

Monitor your viable and non-viable particles according to the most recent regulatory requirements. Count, report, document and manage your pharmaceutical environmental monitoring data meeting 21 CFR Part 11 data integrity requirements.

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Particle Measuring Systems

BSL-3 cGMP Modular Facility Tour

From biosafety protocols to cGMP compliance, Germfree's Chief Operating Officer sheds light on the facility's operational excellence and its significance in advancing the commitment to delivering top-tier solutions in biosafety and pharmaceutical manufacturing.

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Germfree

Vaporized Hydrogen Peroxide Biological Indicators

APEX Biological Indicator products are designed specifically for the pharmaceutical and medical device industries utilizing H2Ovapor sterilization. The stainless steel carrier is designed for use with today’s isolator and filling line applications.

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Mesa Laboratories

EMPQ And Validation Support Services

A growing pharma/biotech company hired a global consulting firm for a project that required EMPQ services for qualification activities on a newly completed aseptic processing suite.

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CAI

Pharmaceutical Cleanroom Facilities For Sterile Drug Manufacturing

Injectable product manufacturing facilities represent the most sophisticated and challenging to design, build, qualify and operate, since products manufactured in these facilities are rendered sterile when complete, ready to inject directly into a human.

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AES Clean Technology, Inc.

Access cGMP Biomanufacturing Capacity Faster

Discover a software solution that enables the rapid, pretested, and pre-verified integration of your bioproduction equipment into a central data storage, visualization, and reporting infrastructure.

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Cytiva