Cleanroom Operations - particlesciences.com

1 2010 Particle Sciences, Inc. All rights of ContaminationIn order to control contamination, operators and those in charge of a Cleanroom need to be cognizant of sources of contamination. These include: 1. Facilities: walls, floors and ceilings; paint and coatings; spills and leaks2. People: skin flakes and oil; cosmetics and perfume; spittle; clothing debris (lint, fibers, etc.); hair3. Tool-generated: friction and wear particles; lubricants and emissions; vibrations; brooms, mops, and dusters4. Fluids: particulates floating in air; bacteria, organics, and moisture; floor finishes or coatings; cleaning chemicals; plasticizers (outgasses); water5.

2 Product-generated: glass flakes; Cleanroom debris; aluminum particles from vial capsKey Elements of Contamination Control Cleanroom Architecture Cleanrooms are designed to achieve and maintain an airflow in which essentially the entire body of air within a confined area moves with uniform velocity along parallel flow lines. This air flow is called laminar flow. The Cleanroom OperationsBackground Cleanrooms are defined as a room or suite of rooms, in which the concentration of airborne par-ticles is maintained within estab-lished parameters and where other factors are controlled to within specified limits. These rooms are designed to provide control of en-vironmental factors including: Viable and non-viable airborne particles Air flow patterns Temperature and humidity Air pressure differential Containment of hazardous aerosolsApplications include the manu-facture of sterile and non-sterile pharmaceutical and biotech prod-ucts, medical devices, and im-plants.

3 These rooms are also used to manufacture sensitive electron-ics. However, the requirements for these latter applications are not the objective of this article. GMP requirements from the different Boards of Health, including the US Food and Drug Administration (FDA), for sterile pharmaceutical, biotech, medical devices and im-plants require the manufacture of these products are performed in clean environments that meet the requirements of standards such as ISO EN146441. Compliance Requirements: FDA Guideline Sterile Drug Products Produced by Aseptic Processing2 European Union (EU) GMP Annex 13 Manufacture of Sterile Medicinal ProductsOther Helpful Documents: ISO EN14644-1, -2 International Society for Phar-maceutical Engineering (ISPE4)Air Handling RequirementsRoom air should be supplied by an external air conditioning system, preferably dedicated to the facility.

4 Partial recirculation of room air is appropriate and this allows for optimal energy utiliza-tion. Sufficient fresh air should be supplied in accordance with ven-tilation codes, to balance exhaust air and to maintain specified pres-sures. Unless, otherwise speci-fied, typical temperature range for this kind of room is within the range of 16 to 19 C and relative humidity of approximately 50% is maintained. The type of equip-ment and number of people in the room may dictate where in the range you need to be to assure that during production the Operations area is maintained at the right temperature and humidity HEPA filtered air should enter the Cleanroom and the gown-ing areas.

5 These modules are available in fan assisted with fan speed control and should oper-ate at a velocity of 90 10 fpm or m/s. The location of the HEPA filters and air return grilles should create air movement from the designated clean zone to the less clean zones. Return air grilles should be at a lower level to aid in laminar flow requirements. Air supply to the Cleanroom should provide a room air change rate of >20 per hour. Air clean-liness will be enhanced by higher air change rates. When the doors are opened the supply air volume should maintain an outward flow of air. Technical Brief 2010 Volume 9more restricted the air flow, the more turbulence and this can cause undesireable particle movement.

6 Filtration In addition to the HEPA filters commonly used in cleanrooms, there are a number of other filtration mechanisms used to remove particles from gases and liquids used in the manufacture of pharmaceutical products. These filters are essential for providing effective contamination control. Cleanroom Garments The requirements for Cleanroom garments will vary from location to location. It is important to know the local Cleanroom garment requirements. Gloves, face masks and head covers are standard in nearly every Cleanroom environment as well as coveralls. Personnel - There are both physical and psychological concerns when humans are present in cleanrooms.

7 Physical behavior like fast motion and horseplay can increase contamination. Psychological concerns like comfort, claustrophobia, strong odors, and workplace attitude are important. Below are several ways people produce contamination: Behavior-- Rate of move-ment, sneezing and coughing Attitude-- Work habits and communication between workersPeople are a major source of contamination in the Cleanroom Table 1 Particles/Minute ( )People Activity100,000 5,000,000 100,000,000 Motionless (Standing or Seated)Walking about 2 mphHorseplayTable 2 ISO EN14644 Old Fed Std 209E1001,00010,000100,000 ISO 5 ISO 6 ISO 7 ISO 8 Class A & B*---Class CClass D1710100At 3,52035,200352,0003,520,000*Requirements for particle counts during operation are different from class A, 35,200 particles at In 3,520---3,520,000 Not definedEU GMP Annex 1 Maximum permitted particles per m3 equal to or greater than tabulated sizeMaximum Microbiological Active Air Action Levels (cfu/m3)(Table 1).

8 Notice the number of particles produced per minute during these activities. Cleanroom ClassificationsCleanroom Classifications as specified by different standards are shown in Table 2. Non-sterile products are typically produced in an ISO 8 or EU Class D environ-ment. Sterile products are required to be filled and stoppered in an ISO 5 or EU Class A CleaningAs an example, here are some recommended procedures for cleaning a Class C or ISO 7 Area Cleanroom . These procedures are simply guidelines, not standards or rules. It is important to review all cleaning procedures to be used in a Cleanroom with responsible management.

9 A detailed cleaning schedule should be prepared for every Cleanroom . ProcedureGood housekeeping and main-tenance of the Cleanroom and the associated restricted areas are es-sential to assure quality. Cleaning of an active Cleanroom should be performed daily. However, if the room is not used daily, a different schedule may be implemented, but it should be cleaned after every use. Improper cleaning of the Cleanroom can lead to con-tamination and compromise prod-uct quality. Proper selection of equipment, cleaning agents and cleaning materials is important for proper cleaning. Only prod-ucts that have proven Cleanroom performance records should be considered for use.

10 These prod-ucts should be listed in appropri-ate policies or procedures and all vendors should be informed about the strict policies of how prod-ucts are qualified. All procedures should be strictly enforced. Below are some examples of how to or-ganize Cleanroom cleaning. These are guidelines for preparing work procedures and schedules. Local requirements must be included in any cleaning and Supplies all sup-plies must meet the Class C or ISO 7 Area minimum requirements Cleaning and disinfecting solutions Cleanroom mops Cleanroom vacuum cleaner (if allowed) Cleanroom wipers Cleanroom mop bucket and wringerCleaning Tasks frequency may vary depending upon local require-ments Cleaning of all work surfaces in the controlled environment Vacuuming (if allowed)