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What is cleanroom validation and qualification in pharmaceutical environments?

This article explores cleanroom validation and qualification when it comes to pharmaceutical environments.

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What is the role of single use systems in microbiological environmental monitoring?

This article explores the roles of single use systems, such as microbial sampler impactors, in microbiological environmental monitoring.

United statesAimee molineuxRobert kochJuliusr petriSponsored contentParticle measuring systemsdecParticle measuring systemsImage creditParticle measuringPharmaceutical reviewMeasuring systemsAirborne molecularSurface molecularContent policyNews medical netMicrobiological environmental monitoring

How are pharmaceutical cleanrooms designed to meet GMP regulations?

This article explores how strictly controlled pharmaceutical cleanrooms are designed to reducecontamination risk and meet strict GMP regulations

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Ensuring environmental monitoring solutions meet GMP requirements

This article explores environmental monitoring solutions when it comes to GMP applications.

Aimee molineuxMark hallworthEuropean union volumeEuropean commissionInternational standards organizationSponsored contentParticle measuring systemsdecImage creditParticle measuringLight scattering aerosol particle counterClean areasContamination control strategyFacility monitoring systemEnvironment monitoringEnvironmental monitoring risk assessmentIndustrial automation

Classification of cleanrooms for the pharmaceutical industry

Pharmaceuticals must be manufactured to meet high standards of efficacy and quality. This articleexplores the classification of cleanrooms for the pharmaceutical industry.

Aimee molineuxMark hallworthEuropean commissionEuropean union volumeInternational standards organizationEuropean unionSponsored contentParticle measuring systemsdecParticle measuringGood manufacturing practiceRules governing medicinal productsMedicinal productsVeterinary useSterile medicinal productsGood manufacturing practice revisionMeasuring systems

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