Online Training 2016 - HVAC and GMP Environmental Control - for Pharmaceutical Clean Rooms - By AtoZ Compliance

Key Take Away
Understand the various US and international regulatory requirements for various pharmaceutical clean room classifications on environmental control essential to the manufacture of a quality product.
Overview
Environmental control of pharmaceutical clean rooms is essential to the manufacture of a quality product. Control of such conditions as airborne particulate, micro-organisms, temperature, humidity, differential pressure, airflow, air velocity and personnel is crucial to protect the product from contamination.
Why Should You Attend
It is important that a clean room’s HVAC systems are fully understood, properly designed and properly validated. If this is accomplished, it will provide the environmental control necessary to meet the regulatory particulate and micro-organism levels necessary to manufacture quality pharmaceutical product.
This webinar first details and explains the various US and international regulatory requirements for various clean room classifications.
Next, the webinar provides a comprehensive overview of the mechanics of clean room HVAC. This includes engineering diagrams and schematics. HVAC equipment components are detailed as well as the automated control systems that are available. Clean room design considerations are included. Proper building construction and layout is necessary to achieve both optimum efficiency of the system and optimum cleaning and sanitization of the clean room.
The principles of HEPA filtration are described along with desired clean room airflow patterns and how to achieve them. Proper procedures for HEPA filter leak testing is included.
The webinar then provides valuable information on differential pressure, air velocity, flow rates, and air pressure balancing. Temperature and relative humidity controls and specifications are also detailed. All current air monitoring systems for non-viable particulate and micro-organism measurement are fully reviewed.
Comprehensive procedures for cleaning and sanitization of the clean room environment are presented along with a review of the best disinfectants currently available along with their respective advantages and disadvantages.
The subject of clean room contamination due to personnel is discussed. This includes both gowning technique and aseptic practices.
Finally, a full set of requirements for HVAC system validation is detailed. Ongoing monitoring of the clean room environment is discussed with respect to schedule, specifications and OOS (out-of-spec) actions that may be required.
Areas Covered In This Webinar
GMP Environment
GMP Compliance of Clean Room Environment
Regulatory Clean Room Classification and Requirements
HVAC System Components
Clean Room Design and Layout
HEPA Filtration
Differential Pressure and Air Pressure Balancing Considerations
Temperature and Humidity Controls
Cleaning and Disinfection
Non-Viable Particulate Monitoring Systems
Microbial Monitoring Systems
Personnel Gowning and Aseptic Practices in Pharmaceutical Clean Room
HVAC System Validation
Learning Objectives
The design, validation and ongoing monitoring of a clean room HVAC system is necessary to assure the quality and safety of the pharmaceutical product
A proper understanding and testing of the clean room environment according to international regulatory standards is important from a compliance perspective
Who Will Benefit
Quality Assurance Personnel
Environmental Monitoring Agencies
Microbiology Professionals
Manufacturing Personnel
Validation Professionals
Engineering Professionals
Maintenance Personnel
Speakers Profile
Roger Cowan
Roger Cowan is the founder and owner of R Cowan Consulting Services LLC, a consulting company specializing primarily in the area of pharmaceutical contract manufacturing. Roger has 36 years of experience in pharmaceutical quality assurance and manufacturing. In his career, Roger has held various manager / director positions in Quality Assurance, QC Laboratory, Technical Services Validation, Manufacturing, and Clinical Supply manufacturing and distribution.
Roger has taught courses in microbiology at Seneca College (Pharmaceutical Technology Program) in Toronto, Canada. Roger's areas of expertise include: aseptic pharmaceutical manufacture, GMP facility audits, technical transfer, microbiology, environmental monitoring/contamination control, product sterilization, process development, process validation, clinical supply manufacturing, labeling and distribution, US / International regulatory requirements, regulatory submissions, and quality assurance/control.
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