Transcription of Facility Qualification - PharmOut
{{id}} {{{paragraph}}}
Facility Qualification Eoin Hanley 25 March 2013 Slide 2 PharmOut 2013 References Slide 3 PharmOut 2013 Cleanroom A room in which the concentration of airborne particles is controlled, and which is constructed and used in a manner to minimise the introduction, generation and retention of particles inside the room, and in which other relevant parameters temperature, humidity and pressure, are controlled as necessary ISO 14644-1:1999 Willis Whitfield Inventor of the modern cleanroom (1919 2012) Slide 4 PharmOut 2013 ISO 14644-1:1999 Slide 5 PharmOut 2013 Room grades ISO 14644-1/GMP Annex 1 Slide 6 PharmOut 2013 Airborne Particles Relative Particle size Thickness of Human Hair ~100 m Visible Particle ~50 m m Particle Slide 7 PharmOut 2013 Planning for Facility Qualification design Qualification Requirements Concept design design Drawings & Specs design Approval Installation Qualification Construction Approval Facility Build Commission Operational Qualification Functional Approval Facility Completed (As-Built) Process Equi
Slide 7 © PharmOut 2013 Planning for Facility Qualification Design Qualification Requirements Concept Design Design Drawings & Specs Design
Domain:
Source:
Link to this page:
Please notify us if you found a problem with this document:
{{id}} {{{paragraph}}}
CLEANROOM, Design, Engineering Consulting, Cleanroom Design, World Health Organization, HVAC, INSPECTION OF HORMONE PRODUCT MANUFACTURING FACILITIES, Supplementary guidelines on good, Heating, ventilation and air-conditioning, 31.0 Pharmacy Unit, Bioburden Contamination Control: A Holistic, Bioburden Contamination Control: A Holistic Overview, Risk-Based Environmental Monitoring, Training Course on: Restricted, Training Course on: Restricted Access Barrier Systems RABS