Primary packaging materials for medicinal products. Particular requirements for the application of ISO 9001:2008, with reference to Good Manufacturing Practice (GMP)— 82 стр.
Primary packaging materials for medicinal products. Particular requirements for the application of ISO 9001:2008, with reference to Good Manufacturing Practice (GMP)— 76 стр.
BS EN ISO 14644-16. Cleanrooms and associated controlled environments. Part 16. Code of practice for improving energy efficiency in cleanrooms and clean air devices— 49 стр.
Air filters for general ventilation. Determination of the gravimetric efficiency and the air flow resistance versus the mass of test dust captured— 30 стр.
Cleanrooms and associated controlled environments. Monitoring to provide evidence of cleanroom performance related to air cleanliness by particle concentration— 24 стр.
High-efficiency filters and filter media for removing particles in air. Aerosol production, measuring equipment and particle-counting statistics— 34 стр.
Ceanrooms and associated controlled environments - Part 2: Specifications for testing and monitoring to prove continued compliance with ISO 14644-1 (ISO 14644-2:2000)
Cleanrooms and associated controlled environments - Part 7: Separative devices (clean air hoods, gloveboxes, isolators and mini-environments) (ISO 14644-7:2004)
Field testing of general ventilation filtration devices and systems for in situ removal efficiency by particle size and resistance to airflow (ISO 29462:2013)
