This two-day seminar includes the steps and techniques used to quantify variability in manufacturing processes, and to assure quality products.
The concepts and information presented will be mainly concerned with statistical quality control: obtaining information (data) that is objective, unbiased, and useful for decision making. An emphasis will be placed on the set-up and use of control charts and acceptance sampling systems and procedures.
The objective of the seminar is to provide information that can be used immediately by personnel involved in production operations, and by supervisors and management in decision making. Although the presentation involves use of statistical techniques, presentation of statistical theory will be limited to only what is needed by the attendees to understand and implement processes and testing within the statistical framework.
Presented examples will include an emphasis on the manufacturing processes and quality assurance needs of personnel in the medical device and pharmaceutical industries.
Process and quality control are constantly evolving. Therefore, historical concepts, current trends and regulatory requirements will be discussed. The presentation of statistical charts and analyses, graphical techniques for planning, trouble-shooting and problem solving will also be made.
Areas Covered in the Session
- FDA QSR, ISO 13485:2016, IS 9001:2015 regulations and harmonization
- Overview of statistical theory and nomenclature for processes and quality control
- Variability and risk assessment in practice
- Control before testing!
- Which chart for which process?
- Setting statistical specifications, control limits, and signals
For more information about this conference visit https://www.researchandmarkets.com/research/2f8hrr/2_day_seminar?w=4