Environmental Monitoring of Clean Rooms



Similar documents
CLEAN ROOM MONITORING REGULATORY STANDARDS

Environmental Monitoring

Environmental Monitoring

ENVIRONMENTAL MONITORING

Particle Monitoring Requirements in Pharmaceutical Cleanrooms

Cleanroom. For. Sterile Manufacturing Facilities

The use of risk assessment tools for microbiological assessment of cleanroom environments. by Tim Sandle

International Standard ISO 14644

Understanding USP 797

Manufacturing. Environmental Monitoring Particle Counts Are Easy B IOP ROCESSTECHNICAL. Scott E. Mackler

Qualification of Cleanrooms and Environmental Monitoring - Practical Approaches in Europe

CLASSIFICATION OF CLEANROOMS

Particle Counting and Environmental Monitoring In Pharmaceutical / Life Sciences

EU GMP Annex 1 Update 2008: Airborne Particle Counting

Cleaning. By the end of this chapter, you will be able to: Introduction. Definitions. Chapter 9

Everything you want to know about USP 797

Regulations Concerning

Facility Cleaning & Monitoring. Cleaning

USP <797> Cleanroom Design and Environmental Monitoring. Andrew King, USP <797> Specialist CETA Member RCCP-SC

GMP ANNEX 1 REVISION 2008, INTERPRETATION OF MOST IMPORTANT CHANGES FOR THE MANUFACTURE OF STERILE MEDICINAL PRODUCTS

Air and Water Balancing - Sound and Vibration Testing - Cleanroom Services - Building Commissioning Building Envelope Testing Thermal Imaging

Design, Operation and Management of GTP/GMP Cell Engineering Facilities

Qualification of an Environmental Monitoring Program

BIOLOGICAL SAFETY CABINET PROGRAM

Transferring a Broth Culture to Fresh Broth

Basic Requirements For Aseptic Manufacturing Of Sterile Medicinal Products A Comparison Between Europe And USA

Laminar Flow Cabinets

Cleaning and Disinfection Agenda. 1. Cleanroom Classification. Cleanroom Classification. What does contamination mean? Types of contamination

Validating and Monitoring the Cleanroom

GUIDELINES ON TEST METHODS FOR ENVIRONMENTAL MONITORING FOR ASEPTIC DISPENSING FACILITIES

BEHAVIOUR EXPERIENCE MEDIA FILL QUALIFICATION TRAINING MONITORING GOWNING PERSONAL ATTRIBUTES QUALIFICATION

Lab Exercise 3: Media, incubation, and aseptic technique

Risk-Based Environmental Monitoring. Marsha Stabler Hardiman Senior Consultant Concordia ValSource Wednesday September 17, 2014 FDA/PQRI

ENVIRONMENTAL TESTING & MONITORING: Deciphering Compliance Requirements for Pharmaceutical and Medical Device Manufacturers A WHITE PAPER

CLEAN ROOM TRAINING CLEAN ROOM AREAS

Stainless Steel Worksurface 3 Feet Hood A10-WS-PR3 A10-WS-SR3 4 Feet Hood A10-WS-PR4 A10-WS-SR4 6 Feet Hood A10-WS-PR6 A10-WS-SR6.

Environmental Monitoring Risk Assessment

Trane CleanEffects. Patented technology. Superior performance. READ ONLY

TSI BIOTRAK REAL-TIME VIABLE PARTICLE COUNTER FACILITY MONITORING SYSTEMS

Laminar Flow Cabinets and Workstations

ENVIRONMENTAL MONITORING / TESTING TO CONFORM WITH ISO14644 & TGA GMP REQUIREMENTS

MOHD NASRUL MOHAMAD NOOR

Hazardous Drug. Cleanroom. Standards

LAMINAR FLOW CABINETS

Procedures for the Effective Use of Biological Safety Cabinets

DRAFT GUIDANCE. This guidance document is being distributed for comment purposes only.

Presentation at the 3 rd SAFOODNET seminar

Introduction. Contamination sources

Liabilities of Vented Crawl Spaces And Their Impacts on Indoor Air Quality in Southeastern U.S. Homes

Quality Assurance in Blood Cell Labelling

HVAC Design Requirements

Robert McCabe Director, Health Care Solutions HTS Chicago. Improved Air Quality and Energy Efficiency through Air Handler Filtration System Upgrade

There are several types of air cleaning devices available, each designed to remove certain types of pollutants.

Basics of HVAC Cleaning

SPECIAL APPLICATIONS

Raleigh, NC May 12 th & 13 th Meeting The New ISO Cleanroom Standards And Changing EU Guidance How Will You Comply?

Workflow System for Paperless Air Monitoring Powered by MODA. Presented by

Evaluation of Laminar Flow Microbiological Safety Cabinets

Design, Construction, Commission, and Qualification of Critical Utility Systems: Part III

Risk Based Environmental Monitoring (EM) and EM Data Management and Trending

EUROPEAN COMMISSION ENTERPRISE AND INDUSTRY DIRECTORATE-GENERAL. EudraLex The Rules Governing Medicinal Products in the European Union

Sterile Cleanroom Management

DISCUSSION TOOL PRESENTED TO THE AABB CT REGULATORY AFFAIRS SUBSECTION

A Basic Introduction to Clean Rooms

FDA and the Compounding Pharmacy

patient safety A commitment to GE Healthcare

How To Control A Medical Device With A Pc System

ISOLATOR TECHNOLOGY MANUFACTURING

AccuClean. For Air That s As clean READ ONLY

Indoor Air Quality Issues for Hotels

- WATER DAMAGE RESTORATION -

Microbiological Testing of the Sawyer Mini Filter. 16 December Summary

NNIN Nanotechnology Education

CONTAMINATION CONTROL IN HOSPITALS. Isabelle Pautrel Ingénieur Clean Concept Patriarche & Co i.pautrel@patriarche.fr

Evaluation of Microbial Growth and Survival on Construction materials treated with Anabec NewBuild 30

Infection Prevention + Control

Facility Requirements for the elan2 Office Liquid Nitrogen Generator

TR40 Sterilizing Filtration of Gases A comparison with TR26 Sterilizing Filtration of Liquids

Questions & Answers (Q & A) Regarding Asbestos Treatment with the Fire Suppression and Renovation Project

CLEANROOMS IN PHARMACEUTICAL PRODUCTION

UTILIZATION of PLASMA ACTIVATED WATER in Biotechnology, Pharmacology and Medicine. JSC TECHNOSYSTEM-ECO Moscow, Russia April, 2009

AMENDED January 27, 2015

HEPA-filtered Negative Air Machines and their Role in Creating Airborne Infection Isolation Rooms with the ECU AnteRoom. Frequently Asked Questions

Contamination Control and Environmental Monitoring Systems

Environmental Monitoring of Clean Rooms in Vaccine Manufacturing Facilities

Lecture 30: Cleanroom design and contamination control

Indoor air quality monitoring made easy

Principles. of Pharmaceutical Facility Design. Full Time Part Time Online.

Air Shower Biosafety Changing Station with Pass-Through Box Pass-Through Box Automatic atomizer for no-contact hand disinfection

- WATER DAMAGE RESTORATION -

ASBESTOS MANAGEMENT PROGRAM

Environmental monitoring programme in the cell therapy facility of a research centre: preliminary investigation

White Paper. Life Sciences Industry Solution Blueprint for Environmental Monitoring Systems (EMS) ISPE Guidance and Best Practices.

Cleanroom Solutions Ltd T: F: E: W:

How to Estimate the Cost of a. Laboratory Renovation. Candidate Number:

PERFORMANCE QUALIFICATION OF A CLEAN ROOM FROM A QUALITY PERSPECTIVE

User s Guide. Oreck Air Purifier with HEPA Filtration. Important! Read this manual carefully, and keep for future reference.

Camfil. Technical Services Bulletin Tools for Schools Filtration for Improved Indoor Air Quality

Transcription:

Environmental Monitoring of Raul Duarte President DDK Scientific, Corp. Copyright DDK Scientific, Corp. 2008, 2009, DDK Scientific, Corp. Proprietary

A manufacturing facility for pharmaceutical products and medical devices must be designed with minimizing the introduction, generation and retention of airborne particles in mind. Other parameters that need to be controlled are: air flow filtration, room pressurizations, air velocities, temperature, relative humidity.

Clean rooms must be designed having in mind: Location of the in and out air locks, gowning and de-gowning, door interlocks, visibility, personnel flow, material flow, the introduction of components, location of utilities, location of the equipment inside the clean room.

Class 10,000 Clean Room (GMP facility in an academic center)

Class 10,000 Clean Room (Airflow Diagram)

Two Standards: Federal Standard 209 E ISO 14644 Federal Standard 209 E is easier to understand than ISO 14644 Many companies continue to test their facilities along Federal Standard 209E

(European Union) EUGGMP 2002 Grade A corresponds to: Class 100 M 3.5 & ISO 5 Grade B corresponds to: Class 100 M 3.5 & ISO 5 Grade C corresponds to: Class 10,000 M 5.5 & ISO 7 Grade D corresponds to: Class 100,000 M6.5 & ISO 8

Particles in Outdoor Air Number of Particles / m³ on Outdoor Air Size in Microns >0.1 Dirty 10,000,000,00 0 Normal 3,000,000,000 Clean 500,000,000 >0.3 300,000,000 90,000,000 20,000,000 >0.5 30,000,000 7,000,000 1,000,000

290E ISO1464 4 CLASS 1 0.1µm/m m/m³ 10 0.2µm/m m/m³ 2 0.3µm/m m/m³ 0.5µm/m m/m² 1µm/m³ 5µm/m³ CLASS 2 100 24 10 4 1 CLASS 3 1,000 237 102 35 8 10 CLASS 4 10,000 2,370 1,020 352 83 100 CLASS 5 100,000 23,700 10,200 3,520 832 29 1,000 CLASS 6 1,000,000 237,000 102,000 35,200 8,320 293 10,000 CLASS 7 352,000 83,200 2,930 100,000 CLASS 8 3,520,000 832,000 29,300 1,000,000 CLASS 9 35,200,000 8,320,000 293,000

Maximum permitted number of particles per cubic meter (cubic foot) Grade at Rest in Operation 0.5µm 5µm 0.5µm 5µm A C 100 3,500 (100) 0 3,500 (100) B C 100 3,500 (100) 0 350,000 (10,000) C C 10,000 350,000 (10,000) 2,000 3,500,000 (100,000) D C 100,000 3,500,000 (100,000) 20,000 NOT DEFINED NOT DEFINED

Physical Chemical Biologic Energy Dust Organic Compounds Bacteria Thermal Dirt Inorganic Salts Fungus Light Grit Vapor Spores Electromagnetic (EMI) Fiber Mist Pollen Electrostatic (ESD) Lint Fume Virus Radiation Fly ash Smoke Human Skin Cells Electrical

Schedule of Mandatory Test to Demonstrate Continuing Compliance in Test Parameter Particle Count Test Air Pressure Difference Airflow Class <=ISO 5 >ISO 5 All Classes All Classes Maximum Time Interval 6 Months 12 Months Daily 12 Months

(European Union) EUGGMP 2002 Recommended Limits for Microbial Contamination Grade A B C D Air Sample <1 10 100 200 Settle Plates 90 mm Dia. CFU /m³ <1 5 50 100 Contact Plates 55 mm Dia. CFU / m³ m <1 5 25 50 Glove Prints 5 Fingers CFU / Glove <1 5 - -

GRADE CLASS TYPE OF ASEPTIC OPERATIONS A 100 Aseptic Preparation and Filling B C D 100 Room Conditions for Activities Requiring Grade A 10,000 Preparation of Solutions to be Filtered 100,000 Handling of Components after Washing

Clean Room Environmental Monitoring TEST Particle Monitoring in Air HEPA Filter Integrity Testing Air Change Rate Calculation Air Pressure Differentials Temperature and Humidity Microbial Monitoring by Settle plates and /or Swabs in Aseptic Areas FREQUENCY 6 Months Yearly 6 Months Daily Daily Daily, and at Decrease Frequency in other Areas

Air Classification by FDA Guideline on Sterile Drug Products CLEAN AREA <0.5µm <0.5µm CLASSIFICATION Particles / ft³ Particles /m³ Microbiological Limits cfu / ft³ cfu /m³ 100 100 3,500 <1 <3 1,000 1,000 35,000 <2 <7 10,000 10,000 350,000 <3 <18 10,0000 100,000 3,500,000 <25 <88

Special Requirements for ISO Class 3 (290E Class 1) Air Quality Total Hydrocarbons <1PPM; Na <0.1 µg/m³ Fresh Air Intake 0.5 m³ m / min per m² m of Clean Room Area Vibration <0.1 µ (Building); <0.01 µ (Equipment) Rooms Noise <55 dba Temperature 0.1 Degree C Humidity <2% Magnetic Field <1mG Static Charge <50 v

Clean Room Industry Design Rule of Thumb ISO Class Controls Air Velocity Air Changes HEPA fpm per Hour Coverage 1 Stringent 70-130 >750 100% 2 Stringent 70-130 >750 100% 3 Stringent 70-130 >750 100% 4 Stringent 70-130 500-600 100% 5 Stringent 70-90 150-400 100% 6 Intermediate 25-40 60-100 33%-40% 7 Intermediate 10-15 15 25-40 10%-15% 15% 8 Less Stringent 3-5 10-15 15 5%-10%

Air Particle Counting Federal Standard 209E calculates a minimum of 12 locations ISO 14644 calculates a minimum of 9 locations

Air Particle Counting Base Line Take three one-minute, one-cfm (28.3 liters) samples per location for better statistical reliability. Test Laminar Flow work stations and Barrier isolators the same way. Testing should be done every six months or after any repairs, or renovations. When sampling, test for viable organism at the same time.

Elements of a Microbial Monitoring Program Sampling Methods Media & Incubation Conditions Sampling Locations Frequency of Sampling Alert & Action Limits Trend Analysis Out of Limits Investigations Corrective Action

The selection of sampling locations depends on the room classification, design, layout of the manufacturing process. Each process should be evaluated in order to identify the actual and potential sources of contamination.

A diagram of the sampling locations must be done as well as documenting the procedure of collecting, incubate and analyze samples.

Class 10,000 Clean Room Touch Plate Sampling Points

Sampling must occur at the same location each time and at the same time of the day.

Air Sampling - Microbial Sieve Impaction Sieve to Air Samplers Centrifugal Impaction Reuter Centrifugal Sampler Plus Filtration MD-8 8 Air Sampler Slit Impaction Slit to Agar Air Sampler Settling Plates

Microbial Air Samplers Basic Principals Microbial Air Samplers collect a predetermined volume of air and impact microorganisms against agar-based growth medium. Once that sample has been collected and the medium incubated, the results are expressed in colony forming units per cubic meter.

Microbial Air Samplers The most common impaction portable air samplers are: Centrifugal Impaction: It utilizes a rotor device in the head of the air sampler to draw air and microorganisms in and onto a special strip containing growth medium. The centrifugal force causes particles and microorganisms to impact the medium at a rate dependent on the size of the particle.

Microbial Air Samplers Sieve Impaction: Is based on the aspiration of air through small holes at the top of the sampler. A Petri dish containing growth medium sits in a holder and a perforated lid locks in place over the medium. A fan mechanism is placed bellow and draws air through the lid. The air directly impacts the Petri dish, forcing the microorganism to stick to the surface of the Agar. The impaction speed as well as particle size efficiency is a function of the holes in the perforated lid and the fan speed. This allows particles as small as 1 micron in diameter at a single flow rate.

Surface and Personnel Sampling Surface Rinse Method RODAC Plate Method Swab Method ATP Bioluminescence Hygiene Monitoring Method

Microbial Monitoring Frequency Air, Surfaces and Personnel Monitoring Should be done Frequently During Aseptic Operations Product Contact Surfaces Should be Monitored at the End of the Aseptic Operation

Monitoring Sites Air monitoring should be done adjacent to the filling location. Product contact surfaces areas, non contact areas, open vials, stopper track, etc. Personnel monitoring should be done at the sleeves and gloves.

Air Monitoring Limits Class 100 and Class 1,000 Critical processing areas for product and containers Less than 3 cfu per cubic meter of air or 0.1 cfu per cubic foot. Frequency: Each shift

Air Monitoring Limits Class 10,000 Less critical processing areas for product and containers. Less than 20 cfu per cubic meter of air or 0.5 cfu per cubic foot. Frequency: Daily

Clean rooms Limits Air Monitoring Class 100,000 Controlled support areas 100 cfu per cubic meter of air or 2.5 cfu per cubic foot Frequency: Twice per week

Surface Monitoring Limits Class 100 and 1,000 Critical processing areas for product and containers 3 cfu per 30 square centimeters or 2 square inches RODAC plate. 5 cfu per 30 square centimeters or 2 square inches RODAC plate for the floor. Frequency: Each shift

Class 10,000 Less critical processing areas for product and containers. 5 cfu per 30 square centimeters or 2 square inches RODAC plate. Frequency: Surface Monitoring Limits Daily

Note: Environmental Monitoring of Personnel involved in the manufacturing, packaging processes generally contribute with most of the viable contamination.

Class 100 and 1,000 Critical processing areas for product and containers 3 cfu per glove (30 square centimeters) 5 cfu per gown (30 square centimeters) Frequency: Personnel Monitoring Limits Each shift

Personnel Monitoring Limits Class 10,000 Less critical processing areas for product and containers 10 cfu per glove (30 square centimeters) 20 cfu per gown (30 square centimeters) Frequency: Daily

Setting Limits Limits should be consistent with regulatory and compendial guidelines. Alert limits should be set from monitoring history

Corrective Action The corrective action plan must be written A check list must be developed for systems review and corrective action. All corrective actions must be documented in a timely fashion.

Conclusions A well designed and executed monitoring plan is a must. The monitoring plan has to be designed using good Judgment so that it can be defended during a compliance audit.

Thank You P.O. Box 23952 Belleville, IL 62223 Phone: (618) 235-2849 2849 Fax: (618) 235-3050 3050 E-mail: rduarte@ddkscientific.com Copyright DDK Scientific, Corp. 2008, 2009, DDK Scientific, Corp. Proprietary