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Cleanroom validation - Germany

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CLEAN PROCESS GMBH

Germany

Clean Process GmbH has been a supplier and partner for air filters, clean room filters and activated carbon since 2016. It was founded by Jens and Nicole Müller (current executive board). We support you with the commissioning and validation of your clean room - If desired, we also prepare maintenance plans and supply replacement filter media - We often create and build special filters & filter solutions for our customers - We support you in implementing your project. In particular we help you ensure compliance with requirements and achieve the required limit values. (Also vis-à-vis public administrations or auditing firms). Our target groups for EPA, HEPA, ULPA suspended particle filters: - Operators of ventilation technology systems, clean rooms or clean room workbenches (laminar-flow workbench) - Operators of extraction systems and air filter systems. What does "CLEAN PROCESS" mean? - The "CLEAN PROCESS" is a "PDCA METHOD" - PDCA is the abbreviation for Plan-Do-Check-Act. - That is our standard procedure - This means we provide our customers (and ourselves) with guaranteed quality from the very outset. Our target groups for activated carbon: - Air filter applications / air purification - solder fumes / 3D printing - water treatment - water purification / decontamination - biogas / desulphurisation - dechlorination / de-ozonisation - decolourisation - electroplating applications.

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ANDJANA INSTRUMENTS UG

Germany

Andjana Instruments offers safe compressed-air quality – air quality monitoring – behind compressors – filters – activated carbon – measuring residual oil content and more: Comprehensive modular compressed air and gas measuring technologies for oil content, volumetric flow, humidity, pressure dew point, particle measurement, pressure, temperature, gases, emissions with optional data acquisition and remote diagnosis according to HACCP – GMP and FDA requirements, ISO 8573, EN 12021 breathing air; validated data records according to FDA 21 Part 11 with audit trail. Metrological safety for industry and hospitals – breathing air systems – laboratories, cleanrooms. Medical hospital breathing air systems according to ISO 7396 – European Pharmacopoeia; risk monitoring for medical compressed air – in-house production in accordance with the Medicinal Products Act; quality control for medical gases – oxygen – nitrogen – compressed air of own production. Standard and CE conformity assessments for medical gas supply systems; job measurements, calibration service, service

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Cleanroom validation - Germany

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