INTRODUCTION FOR ISO 14644 CLEANROOM TRAINING PROGRAM
THE IMPORTANCE OF INDIVIDUAL CLEANROOM AWARENESS.
Cleanroom contamination related failures continue to cost electronics & pharmaceutical manufacturers many millions of dollars every year. The cost of damaged wafers, dies, components, and pharmaceutical products or assembly and pharmaceutical packaging might be only a few cents or could reach thousands of dollars. When particle contamination happens in a cleanroom environment, multiply the cost by ten. Airborne particle contamination can impact production yields, product quality, reliability in the field, and customer satisfaction, all of which will affect your profitability.
Current industry standards including ISO 14644 call for an effective Cleanroom control program that includes initial and recurrent Cleanroom awareness training for all personnel who might come into the Cleanroom area, and for the maintenance of complete training records.
The Workshops will help you to:
- Understand Cleanroom impact in the electronics & pharmaceutical environment
- Determine Cleanroom controls problems
- Establish & implement techniques to measure and audit your plant and Cleanroom Control Plan
- Establish, implement and verify a Cleanroom control plan as per ISO 14644 & GMP
WHO SHOULD ATTEND
Managers, Engineers, Technicians, Supervisors, and any personnel handling Cleanroom sensitive items. Relevant for Semiconductor, PCB Assembly, Disk Drive, Wafer Fabrication, Fiber Optics, Electronics manufacturing industries, and Pharmaceutical industries (GMP).
COURSE CONTENTS
Day 1: 9.00am – 5.00pm
Cleanroom Fundamentals
MODULE 1:
- Purpose of clean protocol
- Introduction & Classification
- Types of contamination, Contamination sources & control
- Cleanroom environment monitoring
Cleanroom Design & Construction
MODULE 2:
- Facility design & Layout
- Air change rate & Airlocks
- Pressurization
- Temperature & Humidity control
- Gowning room
- Pass-through
- Sitting
Cleanroom Materials
MODULE 3: Materials for Construction
- Wall & Wall finishes
- Ceiling, Door & Floor
Day 2: 9.00am – 5.00pm
HVAC & Filtration Systems
MODULE 4:
- Airside & Filtration
- Filter Locations
Cleanroom Testing
MODULE 5:
- Testing procedures and standards
Utilities
MODULE 6:
- Essential utilities for cleanroom operations
VDA 19.2 Requirements
MODULE 7:
- Overview of VDA 19.2 standards and compliance
METHODOLOGY
Seminar consists of 2 days of training workshop.
Workshop 1
- Cleanroom Fundamentals
- Cleanroom Design & Construction
Workshop 2
- Cleanroom Materials
- HVAC & Filtration Systems
- Cleanroom Testing
- Utilities
- VDA 19.2 Requirements
The fundamental workshop will give an insight into the cleanroom purpose and requirements and why a cleanroom environment is required. This module will examine critical selection criteria for determining the most efficient and cost-effective cleanroom construction technique.
