Cleanroom cleaning products
SECTION 013513.11 - CLEANROOM CONSTRUCTION PROCEDURES
Division 01 Section "Cleanroom Special Construction and Cleaning Procedures". Division 01 Section "Cleanroom Certification and Acceptance". REFERENCES . General: The following documents form part of the Specifications to the extent stated. Where differences exist between codes and standards, the one affording the greatest protection shall apply. Unless otherwise noted, the referenced standard ...
[DOC File]Why Cleanrooms
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2004-11-15 · Cleaning a cleanroom is more difficult than cleaning, say, a dirty window. In large part this is because in many cases you are cleaning dirt that you can not see, and are not even certain you are removing the contamination via cleaning. Most readers of these notes will not clean cleanrooms professionally; nevertheless, you should know something about such cleaning. Like many other …
[DOCX File]CLEANROOM FLUSH FILTERED CEILING GRID [AND PLENUM] …
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PART 2 - PRODUCTS. ACCEPTABLE MANUFACTURERS. Clean-Trak [and PlenPAK] as manufactured by CLEANPAK.FILTERED CEILING GRID SYSTEM. The grid system shall be the Clean-Trak Top-Load Extruded Aluminum Gel-Seal Flush Ceiling Grid. Grid shall have an integrated top facing trough to hold gel for a knife-edged top-load filter. The ceiling grid system shall consist of a grid of powder coated …
SECTION 013513.12 - CLEANROOM SPECIAL CONSTRUCTION …
PRODUCTS. MATERIALS. CREW 2 or equivalent cleanroom wipe. DeIonized water. 10 percent Isppropyl Alcohol 90 percent DeIonized water solution . Disposible sticky roller – cleanrrom rated. Cleanroom Detergent: Manufacturer TBD. EXECUTION. CLEANING. General: The tasks of the specialty cleaning subcontractor are described as follows: Responsible for maintaining cleanliness in the cleanroom …
[DOCX File]Section 23 40 00 - HVAC AIR CLEANING DEVICES
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//2.10 Chemical Media Gas-Phase Air Cleaning Cassettes – Heavy Duty (HD) Cassette, Medium Duty (MD) Cassette, Cleanroom Grade (CG) Cassette A.Performance Characteristics 1.The chemical filters shall be as described in the following table and shall have a pressure drop, under operating conditions, no greater than those shown.
[DOC File]Good Manufacturing Practices (GMP’s) Policy
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This is not only to protect our products from contamination, but also to protect you from injury and/or the loss of a valuable possession. (Skin area underneath jewelry is a warm area and together with moisture and a little air, these are ideal conditions for bacteria to grow at a rapid rate). Hands. Your hands can be the source of many microorganisms. The following rules apply to you: You ...
[DOC File]Packaging Safety Supplies Janitorial Cleanroom Disposables
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Quality Products On-Time Deliveries Professional Courtesy. Real People….. Not Voice Mail . If you need SERVICE call Craftsman Packaging (510) 441-7447 Custom Packaging Cushioning Shipping Supplies Corrugated Bubble Wrap Bags Retail Folding Cartons Flowable Loose Fill Boxes Produce & Bakery Bags Biodegradable Foam Desiccant Plastic Boxes & Totes Fabricated Foam Kraft Paper Thermoformed ...
[DOCX File]PE009, the PIC/S guide to GMP for medicinal products
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You are responsible for demonstrating that the applied cleaning and sanitisation procedures are suitable for its intended purpose. This can be demonstrated by qualification, validation and monitoring studies. The extent of these studies will depend on the nature and types of products manufactured and the associated risks of contamination. Cross-contamination and dedicated facilities. Prevent ...
[DOCX File]Guide: GMP checklist for ATMP manufacturers
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Advanced therapy medicinal products that are administered to patients under Article 3(7) of Directive 2001/83/EC1 (so called “hospital exemption”) must be manufactured under equivalent quality standards to the manufacturing of advanced therapy medicinal products with a marketing authorization.” How to use this guide: This checklist should be used as a guidance for the understanding and ...
[DOCX File]Control of Documents SOP
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Cleanroom – Class 1K, 10K or 100K cleanroom, depending on the stringency of the particle counts allowed for the manufacturing activities of the medical devices. A Class 1K cleanroom is designed to never allow more than 1000 particles (0.5 microns or larger) per cubic foot of air. Class 10K and Class 100K cleanrooms are designed to limit particles to 10,000 and 100,000 respectively. Refer to ...
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