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Assessing the implementation of microplate readers in regulated environments

This article explores the implementation of Molecular Device's microplate readers in regulated environments.

United kingdomAimee molineuxCertified field service engineers fsesProducts servicesClinical laboratoryResearch useEuropean unionAnalysis softwareGood laboratory practiceHuman servicesOffice of national drug controlDrug enforcement administration department of justiceMolecular devices united kingdom ltdDrug administrationLaboratory recordsDepartment of health

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

Philogen S p A announces receipt of the Good Manufacturing

Philogen S p A announces receipt of the Good Manufacturing
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New zealandUnited statesDuccio neriDario neriRosia sienaEuropean parliamentEuropean unionEuropean commissionAgenzia italiana del farmacoGood manufacturing practiceEuropean member stateRules governing medicinal productsMedicinal productsExecutive chairman

Philogen S p A announces receipt of the Good Manufacturing Practice Certificate for its new Production facility in Rosia (Siena, Italy) by Competent Authorities

SIENA, Italy, Dec. 05, 2023 Philogen S.p.A. is pleased to announce that its new GMP facility located in Rosia Siena, is now GMP certified. The certification was granted by the GMP MED office of.

New zealandUnited statesDuccio neriDario neriRosia sienaEuropean parliamentEuropean unionEuropean commissionAgenzia italiana del farmacoGood manufacturing practiceEuropean member stateRules governing medicinal productsMedicinal productsExecutive chairman