The core activity of Complean is the planning, implementation and qualification of cleanrooms and production facilities, particularly in regulated areas such as the pharmaceutical industry. This also includes the execution of qualification and validation tests, the creation of documentation and the accompaniment of commissioning. Complean also offers monitoring solutions for the monitoring of process data and the capture of physical parameters.
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Industry:Technical Consulting & Engineering
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Design of cleanrooms to ISO 14644, VDI 2083 or GMP; needs analysis, development of URS and specifications, 3D modelling, definition of requirements and regulatorily compliant concept development.
Implementation & construction
Implementation and construction of cleanrooms; bid management, awarding, site management, construction supervision, quality control, coordination of all trades, and schedule and cost control.
Commissioning
Commissioning of cleanrooms; technical verification, system tests, ventilation technology, filter technology, monitoring, documentation, staff instruction and turnkey handover.
Qualification (GMP)
Qualification of cleanrooms and facilities according to GMP; DQ, IQ, OQ, PQ, evidence of compliant operation, traceability and audit-ready documentation.
Measurement technology
Cleanroom measurements to ISO 14644 and GMP Annex 1; particle measurements, filter scanning, airflow and pressure measurements, recovery time measurement, microbiology, flow visualisation and reports.
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