Clean Room - A compendium according to approved guidelines.Md Mosaruf Hossan
The document provides an overview of cleanroom classifications according to ISO, US Federal Standard 209E, and European standards. It discusses particle sources and control methods like filtration, dilution with higher air changes, and isolation. PIC/S guidelines recommend grade A environments with precise air control for high-risk aseptic operations, and grade B-D cleanrooms for less critical stages. Microbial limits and air monitoring frequencies are specified depending on the cleanroom grade.
Cleaning and Disinfecting the CleanroomPeter Lojac
Cleaning and disinfecting your cleanroom environment is the only way to maintain its efficacy. This presentation explains the cleanroom cleaning methods and types of contaminants.
This document discusses different standards for classifying cleanrooms according to airborne particle concentrations. It describes the obsolete Federal Standard 209 classification system used in the US which categorizes cleanrooms from Class 1 to Class 10,000 based on particle counts per cubic foot. It then outlines the ISO 14644 international cleanroom standards which use particle counts per cubic meter and have classifications from ISO 1 to ISO 9. The document provides tables comparing particle concentration limits between the two systems. It also discusses pharmaceutical cleanroom classifications used in the European Union and US which are based on maximum permitted particle counts for different operations.
The document outlines cleanroom rules and practices that personnel should follow to minimize contamination. It states that cleanroom employees should be neat, clean and in good health. They must also have a minimum education level and understand aseptic techniques. Strict rules are outlined, including washing hands before entry, slow movement, limiting talking and activities that increase particles, and not bringing in unauthorized items. Personnel are instructed to avoid interrupting airflow, touching products directly and exposing them unnecessarily. Failure to follow the rules could lead to increased contamination from people, who are the main source of particles in cleanrooms.
This document discusses the design and operation of clean rooms. It explains that clean rooms carefully control airborne particles and other parameters like temperature, humidity, and pressure. Clean rooms use HEPA and ULPA filters with either laminar or turbulent air flow. The document then discusses how to design an ideal clean room that meets ISO standards for aseptic processes. It emphasizes easy cleaning, durable materials without cracks or gaps, and maintaining air quality through regular testing and procedures.
This is the 1st part of our "All about cleanrooms". This presentation will take you through the history of cleanrooms, types and applications of cleanrooms.
The document discusses cleanroom protocols and procedures. It defines cleanrooms and their importance for minimizing contamination, especially in semiconductor manufacturing. It outlines cleanroom classifications, air filtration systems, environmental controls, and guidelines for cleaning, materials selection, and user behavior. Strict adherence to cleanroom protocols by all users is emphasized as essential for maintaining the clean environment.
Clean Room - A compendium according to approved guidelines.Md Mosaruf Hossan
The document provides an overview of cleanroom classifications according to ISO, US Federal Standard 209E, and European standards. It discusses particle sources and control methods like filtration, dilution with higher air changes, and isolation. PIC/S guidelines recommend grade A environments with precise air control for high-risk aseptic operations, and grade B-D cleanrooms for less critical stages. Microbial limits and air monitoring frequencies are specified depending on the cleanroom grade.
Cleaning and Disinfecting the CleanroomPeter Lojac
Cleaning and disinfecting your cleanroom environment is the only way to maintain its efficacy. This presentation explains the cleanroom cleaning methods and types of contaminants.
This document discusses different standards for classifying cleanrooms according to airborne particle concentrations. It describes the obsolete Federal Standard 209 classification system used in the US which categorizes cleanrooms from Class 1 to Class 10,000 based on particle counts per cubic foot. It then outlines the ISO 14644 international cleanroom standards which use particle counts per cubic meter and have classifications from ISO 1 to ISO 9. The document provides tables comparing particle concentration limits between the two systems. It also discusses pharmaceutical cleanroom classifications used in the European Union and US which are based on maximum permitted particle counts for different operations.
The document outlines cleanroom rules and practices that personnel should follow to minimize contamination. It states that cleanroom employees should be neat, clean and in good health. They must also have a minimum education level and understand aseptic techniques. Strict rules are outlined, including washing hands before entry, slow movement, limiting talking and activities that increase particles, and not bringing in unauthorized items. Personnel are instructed to avoid interrupting airflow, touching products directly and exposing them unnecessarily. Failure to follow the rules could lead to increased contamination from people, who are the main source of particles in cleanrooms.
This document discusses the design and operation of clean rooms. It explains that clean rooms carefully control airborne particles and other parameters like temperature, humidity, and pressure. Clean rooms use HEPA and ULPA filters with either laminar or turbulent air flow. The document then discusses how to design an ideal clean room that meets ISO standards for aseptic processes. It emphasizes easy cleaning, durable materials without cracks or gaps, and maintaining air quality through regular testing and procedures.
This is the 1st part of our "All about cleanrooms". This presentation will take you through the history of cleanrooms, types and applications of cleanrooms.
The document discusses cleanroom protocols and procedures. It defines cleanrooms and their importance for minimizing contamination, especially in semiconductor manufacturing. It outlines cleanroom classifications, air filtration systems, environmental controls, and guidelines for cleaning, materials selection, and user behavior. Strict adherence to cleanroom protocols by all users is emphasized as essential for maintaining the clean environment.
The document provides guidance on basic cGMPs (current Good Manufacturing Practices) for pharmaceutical manufacturing. It discusses requirements for quality management, facilities and equipment, raw material control, production processes, laboratories, warehousing, documentation, gowning procedures, and sterile drug production. The key points are that cGMPs ensure minimum standards for quality are met, personnel must be properly trained and attired to prevent contamination, facilities and equipment must be cleaned and maintained, raw materials must be tested and stored securely, and processes must be documented thoroughly.
Clean rooms are controlled environments used to manufacture pharmaceuticals and medical devices where airborne particle levels are strictly limited. Federal Standard 209E specifies cleanroom air cleanliness levels. A Class 100 cleanroom allows no more than 100 particles per cubic foot of air, while Class 1000 and Class 10,000 allow 1000 and 10,000 particles respectively. Contamination can originate from facilities, humans, tools, fluids, and products, so cleanrooms must be carefully designed, filtered, cleaned, and have contamination control procedures to maintain the required air purity levels.
Cleanrooms require strict control of contaminants and careful maintenance of temperature, humidity, air pressure, and filtration to protect sensitive work in electronics manufacturing and pharmaceutical production. Key requirements for cleanrooms include filtering outside air of dust and particles, continuously recirculating and scrubbing interior air through additional filters, regulating climate control, using positive or negative air pressure techniques, and employing multi-stage airlocks to purge unfiltered air before personnel entry. Cleanroom standards help ensure contaminant-free environments for tasks like semiconductor chip-making and drug development that demand pristine conditions.
Cleanroom clothing - Why, what and how?Heidi Tuomi
Cleanroom clothing is worn to protect cleanroom environments and products from human contamination. People are the largest source of particles in cleanrooms, shedding skin cells and microbes. Cleanroom clothing must filter these contaminants and include head covers, body suits, gloves, boots, and face masks appropriate for the cleanroom class. The clothing is donned in a changing room process to minimize contamination entering the cleanroom.
1) As a clean room design consultant, we help medical device manufacturers design clean rooms to strict ISO standards to minimize airborne particles and control environmental factors.
2) Clean rooms are facilities designed and operated to control pollution such as dust, microbes, and chemicals according to ISO 14644 clean room standards.
3) We design clean rooms to maintain low air particle levels as specified by ISO 13485 and ISO 14644 clean room design standards to ensure medical device quality and safety.
To maintain the desired SAL at the plant is task which demands great care and control over Man, Machine & Method. This summarize work will definitely help you as hand note.
The document provides an overview of cleanroom and cleanzone protocols. It discusses cleanroom basics like definitions, components, construction stages, apparel requirements and other protocols. The key aspects covered are preventing dust entry, minimizing dust generation, removing dust, and not accumulating or scattering dust. Cleaning protocols like daily and regular cleaning are also summarized. The document aims to educate people on cleanroom requirements and practices to maintain cleanliness.
The document provides an overview of clean rooms, including their purpose, key components, classification standards, and importance in the pharmaceutical industry. A clean room is a controlled environment designed and maintained to reduce contamination through strict control of particulate matter and other pollutants. Clean rooms are classified based on standards like ISO and use HEPA filters to purify air circulation. Proper clean room certification and validation is important for ensuring safety and quality in pharmaceutical manufacturing as required by cGMP guidelines.
El documento describe la técnica del lavado quirúrgico de manos, el cual incluye quitarse joyería, cortarse las uñas, lavar y cepillar las manos y antebrazos durante varios minutos usando jabón antiséptico para eliminar gérmenes y reducir el riesgo de contaminación en procedimientos quirúrgicos. Explica los pasos a seguir, incluyendo lavar, enjuagar y secar las manos y brazos de forma minuciosa.
A clean room is an environment with controlled levels of particulate contamination defined by international standards. Clean rooms minimize introduction and retention of particles through HEPA filtration of air, controlled airflow, temperature, humidity and pressure. Contamination is classified as particulate, chemical, biological or radiation. People are the largest contamination source. Clean rooms require strict personal hygiene, protective clothing, and environmental controls to maintain the clean environment for pharmaceutical manufacturing as defined by regulations like ISO, GMP and FDA standards.
Clean room technology is used to control airborne particle concentrations and other parameters like temperature, humidity, and pressure. There are two main types of cleanrooms - turbulently ventilated and unidirectional flow. High efficiency particulate air (HEPA) and ultra low penetration air (ULPA) filters are used to filter air and control particle levels, working via mechanisms like diffusion, impaction, interception, and sieving. Proper clean room practices like changing gloves, wiping surfaces, and avoiding contaminants are important for maintaining cleanliness.
This document discusses key considerations for the aseptic manufacturing of sterile pharmaceutical products. It covers classification of clean areas, environmental monitoring, preparation and filtration of solutions, personnel requirements, equipment sterilization, and validation of aseptic processes. The main objectives are to prevent microbial contamination and maintain sterility throughout manufacturing.
“Gowning” is a set of garments worn while in a clean room or other controlled environment. The
level of gowning required is a function of the product or process, and its cleanliness
requirements.
Gowning can cover some or all of the following:
Head / hair
Beard / mustache
Face
Torso / Upper body
Legs / pants
Feet / shoes
Hands
This document outlines standards of behavior and practices for cleanrooms and cleanzones. It defines key terms like cleanroom, cleanzone, critical activity, and aseptic processing. The document provides guidelines for behaviors in all cleanrooms and cleanzones, including proper gowning, minimizing contamination, and maintaining orderly work areas. It also outlines additional requirements for aseptic filling suites, such as proper glove sanitization procedures and using aseptic technique. The document states that compliance with these standards will be assessed through microbiological audits and is necessary to meet regulatory expectations for sterile drug production.
The document summarizes a presentation for parents on motivation, enthusiasm, and underachievement. It discusses how engaged preschoolers can become underachieving adolescents due to mixed messages received as they grow up. Common causes of underachievement like health issues, family events, relationships, and school experiences are explored. Six practical steps for developing motivation are outlined: creating an achievement environment, avoiding power struggles, building relationships, providing challenges and support, setting goals, and focusing on success. The presentation emphasizes adopting a growth mindset and recognizing effort over outcomes to foster motivation.
The document provides guidance on basic cGMPs (current Good Manufacturing Practices) for pharmaceutical manufacturing. It discusses requirements for quality management, facilities and equipment, raw material control, production processes, laboratories, warehousing, documentation, gowning procedures, and sterile drug production. The key points are that cGMPs ensure minimum standards for quality are met, personnel must be properly trained and attired to prevent contamination, facilities and equipment must be cleaned and maintained, raw materials must be tested and stored securely, and processes must be documented thoroughly.
Clean rooms are controlled environments used to manufacture pharmaceuticals and medical devices where airborne particle levels are strictly limited. Federal Standard 209E specifies cleanroom air cleanliness levels. A Class 100 cleanroom allows no more than 100 particles per cubic foot of air, while Class 1000 and Class 10,000 allow 1000 and 10,000 particles respectively. Contamination can originate from facilities, humans, tools, fluids, and products, so cleanrooms must be carefully designed, filtered, cleaned, and have contamination control procedures to maintain the required air purity levels.
Cleanrooms require strict control of contaminants and careful maintenance of temperature, humidity, air pressure, and filtration to protect sensitive work in electronics manufacturing and pharmaceutical production. Key requirements for cleanrooms include filtering outside air of dust and particles, continuously recirculating and scrubbing interior air through additional filters, regulating climate control, using positive or negative air pressure techniques, and employing multi-stage airlocks to purge unfiltered air before personnel entry. Cleanroom standards help ensure contaminant-free environments for tasks like semiconductor chip-making and drug development that demand pristine conditions.
Cleanroom clothing - Why, what and how?Heidi Tuomi
Cleanroom clothing is worn to protect cleanroom environments and products from human contamination. People are the largest source of particles in cleanrooms, shedding skin cells and microbes. Cleanroom clothing must filter these contaminants and include head covers, body suits, gloves, boots, and face masks appropriate for the cleanroom class. The clothing is donned in a changing room process to minimize contamination entering the cleanroom.
1) As a clean room design consultant, we help medical device manufacturers design clean rooms to strict ISO standards to minimize airborne particles and control environmental factors.
2) Clean rooms are facilities designed and operated to control pollution such as dust, microbes, and chemicals according to ISO 14644 clean room standards.
3) We design clean rooms to maintain low air particle levels as specified by ISO 13485 and ISO 14644 clean room design standards to ensure medical device quality and safety.
To maintain the desired SAL at the plant is task which demands great care and control over Man, Machine & Method. This summarize work will definitely help you as hand note.
The document provides an overview of cleanroom and cleanzone protocols. It discusses cleanroom basics like definitions, components, construction stages, apparel requirements and other protocols. The key aspects covered are preventing dust entry, minimizing dust generation, removing dust, and not accumulating or scattering dust. Cleaning protocols like daily and regular cleaning are also summarized. The document aims to educate people on cleanroom requirements and practices to maintain cleanliness.
The document provides an overview of clean rooms, including their purpose, key components, classification standards, and importance in the pharmaceutical industry. A clean room is a controlled environment designed and maintained to reduce contamination through strict control of particulate matter and other pollutants. Clean rooms are classified based on standards like ISO and use HEPA filters to purify air circulation. Proper clean room certification and validation is important for ensuring safety and quality in pharmaceutical manufacturing as required by cGMP guidelines.
El documento describe la técnica del lavado quirúrgico de manos, el cual incluye quitarse joyería, cortarse las uñas, lavar y cepillar las manos y antebrazos durante varios minutos usando jabón antiséptico para eliminar gérmenes y reducir el riesgo de contaminación en procedimientos quirúrgicos. Explica los pasos a seguir, incluyendo lavar, enjuagar y secar las manos y brazos de forma minuciosa.
A clean room is an environment with controlled levels of particulate contamination defined by international standards. Clean rooms minimize introduction and retention of particles through HEPA filtration of air, controlled airflow, temperature, humidity and pressure. Contamination is classified as particulate, chemical, biological or radiation. People are the largest contamination source. Clean rooms require strict personal hygiene, protective clothing, and environmental controls to maintain the clean environment for pharmaceutical manufacturing as defined by regulations like ISO, GMP and FDA standards.
Clean room technology is used to control airborne particle concentrations and other parameters like temperature, humidity, and pressure. There are two main types of cleanrooms - turbulently ventilated and unidirectional flow. High efficiency particulate air (HEPA) and ultra low penetration air (ULPA) filters are used to filter air and control particle levels, working via mechanisms like diffusion, impaction, interception, and sieving. Proper clean room practices like changing gloves, wiping surfaces, and avoiding contaminants are important for maintaining cleanliness.
This document discusses key considerations for the aseptic manufacturing of sterile pharmaceutical products. It covers classification of clean areas, environmental monitoring, preparation and filtration of solutions, personnel requirements, equipment sterilization, and validation of aseptic processes. The main objectives are to prevent microbial contamination and maintain sterility throughout manufacturing.
“Gowning” is a set of garments worn while in a clean room or other controlled environment. The
level of gowning required is a function of the product or process, and its cleanliness
requirements.
Gowning can cover some or all of the following:
Head / hair
Beard / mustache
Face
Torso / Upper body
Legs / pants
Feet / shoes
Hands
This document outlines standards of behavior and practices for cleanrooms and cleanzones. It defines key terms like cleanroom, cleanzone, critical activity, and aseptic processing. The document provides guidelines for behaviors in all cleanrooms and cleanzones, including proper gowning, minimizing contamination, and maintaining orderly work areas. It also outlines additional requirements for aseptic filling suites, such as proper glove sanitization procedures and using aseptic technique. The document states that compliance with these standards will be assessed through microbiological audits and is necessary to meet regulatory expectations for sterile drug production.
The document summarizes a presentation for parents on motivation, enthusiasm, and underachievement. It discusses how engaged preschoolers can become underachieving adolescents due to mixed messages received as they grow up. Common causes of underachievement like health issues, family events, relationships, and school experiences are explored. Six practical steps for developing motivation are outlined: creating an achievement environment, avoiding power struggles, building relationships, providing challenges and support, setting goals, and focusing on success. The presentation emphasizes adopting a growth mindset and recognizing effort over outcomes to foster motivation.
This document summarizes the Vermont Digital Newspaper Project (VTNDP) which works to digitize historic newspapers from Vermont by first microfilming papers and then digitizing the microfilm. The project receives funding from the National Digital Newspaper Project (NDNP) and works with in-state partners to microfilm and catalog newspaper titles, then sends duplicate microfilm reels and 500-word title essays to the Library of Congress. The project aims to digitize 10,000 pages per month by either contracting a vendor or doing the work in-house according to NDNP technical specifications and timelines. The document provides contact information for the VTNDP librarian.
Enterprise Skills Management (ESM) is a powerful, lightweight and simple SAAS application for mapping and managing employee skills.
ESM's various modules are built around a novel Skills Profiling engine, at the backend of which is the most comprehensive library of skills, one that covers skills across industries.
The functionalities of ESM include Jobs Skills Profiling (JSP), Employee Skills Profiling, recruitment, skills gap analysis, resource management and skills analytics.
Visit www.itsyourskills.com/esm to know more.
A young man uses social media to distract himself from the physical abuse by his elder brother, meeting a girl who temporarily takes his mind off his family problems. As an immature teenager not considering consequences, he gets the girl pregnant after taking advantage of opportunities, becoming a father without realizing it due to his actions. The story board aims to raise awareness of teenage pregnancy by showing how one seeks an escape from abuse through social media leading to an unplanned pregnancy.
This document discusses the complexities of service and how it involves considerations of power, privilege, and relationships. It describes experiences the author had providing service in Ghana and Nicaragua, such as building a water system for a family. While service seems simple, addressing the needs and wants of those being served, overcoming cultural and status barriers, and allowing for mutual understanding and gratitude between parties is complicated. True service requires open communication and establishing caring relationships without any sense of invasion or inequality.
Dokumen ini membahas sejarah penelitian sel sejak abad ke-17, mulai dari penemuan sel oleh Robert Hooke, penemuan organisme mikroskopis oleh Antonie van Leeuwenhoek, hingga pengembangan teori bahwa sel merupakan unit terkecil kehidupan oleh Jacob Schleiden dan Theodor Schwann. Dokumen ini juga menjelaskan perkembangan penelitian sel selanjutnya dan penggunaan mikroskop cahaya dan elektron untuk memp
El documento habla sobre las políticas públicas en Colombia para promover la inclusión educativa mediante el uso de tecnologías de la información y la comunicación (TIC). Aunque el gobierno se ha comprometido a expandir el acceso a internet, muchas escuelas rurales aún no cuentan con la infraestructura necesaria. Además, los maestros no tienen la capacitación para guiar a los estudiantes en el aprendizaje virtual. Por lo tanto, es importante establecer no solo el acceso a las herramientas tecnológicas, sino también
Dokumen ini berisi informasi pribadi seseorang yang meliputi alamat, nomor telepon, tempat dan tanggal lahir, jenis kelamin, tinggi dan berat badan, riwayat pendidikan, hobi dan cita-cita.
A lesson plan for young history detectives on how to research historic buildings using Chronicling America as a primary source. Comes with a handy checklist and worksheet to guide student research.
La pandemia de COVID-19 ha tenido un impacto significativo en la economía mundial. Muchos países experimentaron fuertes caídas en el PIB y aumentos en el desempleo debido a los cierres generalizados. Ahora, a medida que se levantan las restricciones, la recuperación económica será gradual a medida que los consumidores y las empresas se readaptan a la nueva normalidad.
The presentation discusses strategies used by the Vermont Digital Newspaper Project (VTDNP) to promote their work to different audiences. They use various communication channels like their blog, website, social media, webinars and videos. They also give talks at conferences, libraries and for genealogical societies. The VTDNP directors emphasize the importance of saying yes to opportunities to present, which can lead to further opportunities. They discuss initial media releases, press coverage and outreach through presentations, exhibits and workshops. Their goal is to start with small promotional efforts and let them snowball to greater exposure and impact over time.
3. Ihminen epäpuhtauksien lähteenä
Ihminen on useissa tuotantoprosesseissa keskeisessä
roolissa, mutta muodostaa samalla merkittävimmän
kontaminaatiolähteen ja riskin tuotteelle.
Kaikki muu voidaan steriloida tai desinfioida paitsi
ihminen.
80 % puhdastilassa esiintyvistä epäpuhtauksista on
peräisin ihmisistä.
4. Ihmisestä irtoavat epäpuhtaudet
Hilsettä, mikrobeja, kosmetiikkapartikkeleja,
karvoja, vaatekuituja, pölyä
Ihon pintasolukko uusiutuu koko ajan
◦ 10 miljoonaa hilsepartikkelia päivässä
◦ jopa 100 g ihosolukkoa viikossa.
Hiukset ja ihokarvat uusiutuvat, vanhat putoavat
pois
5. Ihminen ja mikrobit
Ihmisessä olevat mikrobit kuuluvat joko
normaaliflooraan tai vaihtuvaan flooraan
1. Normaalifloora
◦ normaaliflooran on elimistössä pysyvästi oleva haitaton
mikrobipopulaatio
◦ normaalifloora on tärkeä ihmisen hyvinvoinnin kannalta
◦ normaaliflooran koostumus vaihtelee eri ihmisillä mm.
iän, sukupuolen, asuinalueen ja vuodenaikojen mukaan
6. Ihminen ja mikrobit
2. Vaihtuva floora
◦ Vaihtuva floora (pääas. iholla) voi sisältää mitä tahansa
mikrobeja, myös patogeeneja
◦ tarttuu ihmiseen ympäristöstä tai toisista ihmisistä
◦ voidaan poistaa iholta pesulla ja desinfioinnilla
◦ tulehduksissa mikrobien määrä esim. iholla tai
limakalvolla voi jopa 1000-kertaistua
9. Ihminen ja mikrobit
IHO päänahka 1,5 x 106 cfu/cm2
käsi 1,0 x 103 cfu/cm2
käsivarsi 1,1 x 102 cfu/cm2
otsa 2,0 x 105 cfu/cm2
SYLKI 107 - 108 cfu/cm3
AIVASTUS 104 - 106 cfu
10. Ihmisestä irtoavat epäpuhtaudet
Irtoavien hiukkasten määrää lisää:
◦ Liikkuminen: kävellessä 10 x verrattuna istumiseen
◦ puhuminen ja yskiminen
◦ tupakointi; uloshengitysilmassa on runsaasti
partikkeleita
◦ kosmetiikan käyttö; levitetään partikkeleja iholle
13. Irtoavien epäpuhtauksien
vähentäminen
Keinoja kontaminaation vähentämiseen:
•Tehokas ja oikein puettu suojavaatetus
•Rauhalliset liikkeet ja oikeat työtavat
•Hyvä henkilökohtainen hygienia
•Terveystarkastukset
SIIS: työntekijöiden koulutus on tärkein keino!
14. Muut ihmisen aiheuttamat häiriöt
Ihminen häiritsee puhdastilan toimintaa paitsi
tuottamalla hiukkasia, myös sekoittamalla
ilmavirtauksia
kun ilmavirtaus kohtaa esteen tai toisen ilmavirtauksen
häiriö
pyörteileviin häiriökohtiin kertyy epäpuhtauksia
16. Käyttäjän vaikutusmahdollisuudet
Käyttäjän mahdollisuudet vaikuttaa puhdastilan
puhtauteen liittyvät
•puhdastilassa työskentelyyn, pukeutumiseen ja
käyttäytymiseen
•materiaalien valintaan ja materiaaliliikenteen
hallintaan
•siivoukseen
17. Yleisiä ohjeita
Kaikkien työntekijöiden henkilökohtainen
vastuuntunto ja ohjeiden kirjaimellinen
noudattaminen on ehdottoman tärkeää.
Selvitä ilman virtaussuunta puhdastiloissa, ettet
asetu suojeltavan tuotteen ja puhtaan ilman tulon
väliin.
18. Yleisiä ohjeita
Puhdastilahuoneen ovista saa vain yksi kerrallaan
olla auki.
Kommunikointi eri puhtausluokkien välillä
hoidetaan puhelimitse, ei sulkujen kautta.
Puhdastilan toimintaa mittaavia laitteita on
seurattava säännöllisesti ja niiden hälytyksiin tulee
reagoida heti.
21. Henkilökohtainen hygienia
Huolehdi puhtaudestasi ja terveydestäsi.
Älä työskentele puhdastilassa sairaana.
Älä käytä kosmetiikkaa äläkä koruja puhdastilassa.
Pidä silmälasisi puhtaana.
Pidä kynnet lyhyenä.
Parta/viikset eivät ole suotavia.
Ihon hilseilyn vähentämiseksi käytä kosteusvoidetta.
Huolehdi myös työasusi puhtaudesta.
22. Puhdastilan liikenne
Tilaan saa kulkea vain henkilösulun kautta.
Älä vie puhdastilaan ylimääräistä/tarpeetonta materiaalia.
Kaikki materiaali viedään puhdastilaan materiaalisulun tai
läpiantosterilisaattorin kautta.
Materiaali puhdistetaan ja desinfioidaan ennen sulkuun
panemista.
Vältä turhaa liikennettä puhdastilaan ja puhdastilassa
Avaa ja sulje ovet hitaasti
23. Käyttäytyminen puhdastilassa
Liiku hitaasti
Työskentele rauhallisin liikkein
Älä koskettele käsilläsi mitään, mihin ei työn suorittamisen
vuoksi ole välttämätön koskea
Älä nojaa käsivarsillasi työtasoon
Älä nojaile tai istu pöydällä
24. Käyttäytyminen puhdastilassa
Älä riisu suojavaatetusta puhdastilan sisällä
Älä kosketa paljasta ihoasi
Vältä koskemasta suojavaatetukseesi
Desinfioi käsineesi riittävän usein
Älä yski tai aivastele puhdastilassa
Keskustele muiden kanssa niin vähän kuin mahdollista
25. Työskentely puhdastilassa
Puhdastilassa tulee olla riittävästi henkilökuntaa, mutta ei
ylimääräisiä.
Opettele tehtävä työ etukäteen.
Käy työvaiheet läpi etukäteen ja varaa työpisteeseesi
tarvitsemasi materiaalit.
Työskentele rauhallisin liikkein.
Pystysuorassa laminaarivirtauksessa älä kumarru tai vie
käsiäsi työkohteen päälle
26. Työskentely puhdastilassa
Älä nosta lattialle pudonneita esineitä.
Käänny poispäin työkohteesta kun puhut.
Avaa ja sulje kannet/laatikot/kaapit hitaasti.
Tavarat säilytetään peitettyinä ja polven korkeuden yläpuolella
Puhdastilan työnjohto hoidetaan ulkoa käsin.
Kantaessasi tarvikkeita älä tue niitä vartaloosi.
27. Työkalut
Puhdastilassa käytettävien työkalujen tulee olla
hyväkuntoisia ja helposti puhdistettavia.
Työkalut on puhdistettava aina käytön jälkeen.
Myös työkalujen säilytyspaikka on puhdistettava
säännöllisesti.