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Facility Validation & Environmental Monitoring

Environmental monitoring in pharmaceutical production from SGS – confirm contamination-free production areas and processes with essential clean room validation, utilities testing, microbiological monitoring services and pharmaceutical process monitoring.
Multichannel Pipette Device Used for Pharmaceutical Research

Confirming that all aspects of your biopharmaceutical and pharmaceutical production process are uncontaminated is vital for meeting your regulatory obligations and ensuring that your products are fit for market. Our environmental monitoring services for pharmaceutical production help confirm that everything from your clean rooms and process media, such as air and gas, right through to your equipment is free from contamination.

We provide customized hygiene-monitoring programs to suit your needs. We also perform acceptance tests for production facility clean room installation and important routine monitoring of viable and non-viable contamination of your production facilities and utilities.

Our services include:

  • Clean room validation
  • Gas monitoring and analysis to demonstrate that regulatory standards have been achieved
  • Water monograph testing performed according to U.S. Pharmacopeial Convention (USP), European Pharmacopoeia (EP) and Japanese Pharmacopoeia (JP)
  • Environmental microbiological testing
  • Microbial and chemical cleaning efficacy and validation studies

As the world-leading provider of environmental monitoring in pharmaceutical production, we offer unrivaled experience, expertise and resources.

To discuss how our environmental monitoring services can help you, contact us today.

Scientists Working in Sterile Pharmaceutical Manufacturing Laboratory

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  • SGS Poland Sp. z o.o.

Al. Jerozolimskie 146A,

, 02-305,

Warsaw,

Poland