Lecture:
1. Quality development and care of quality, economy of quality, technical harmonization and the global approach to conformity assessment
2. General product safety. Manufacturer's obligations when marketing a product, conformity assessment pursuant to Act No. 22/1997 Coll. and procedure to issue an EC Declaration of Conformity
3. Modular concept of demonstrating product conformity, product certification, role of the product certification authority
4. ISO 9000 and ISO 10000 series standards and quality documentation, EN ISO 9001 standard contents and application
5. Quality assurance at the pre-process stage – design (FMEA, QFD), identification of processes and links between processes, constant improvement of processes
6. Management of resources (human resources, material resources, information resources, financial resources), quality system measurements and analyses (customer satisfaction assessment, audits)
7. Constant quality system improvements (corrective and preventive actions, management of non-conformances, audits)
8. Statistical methods - statistical process control, statistical acceptance
9. Quality audits as per ISO 19011
Seminars
1. Quality development and care of quality, economy and quality
2. Basic concepts, quality planning, documentation and records
3. QFD, FMEA, DOE
4. Quality documentation development. Quality manual
5. The 7 "basic" quality tools
6. Seven "new" quality tools
7. Control charts
8. Development of an EC Declaration of Conformity
9. Assessment of the program developed
1. Quality development and care of quality, economy of quality, technical harmonization and the global approach to conformity assessment
2. General product safety. Manufacturer's obligations when marketing a product, conformity assessment pursuant to Act No. 22/1997 Coll. and procedure to issue an EC Declaration of Conformity
3. Modular concept of demonstrating product conformity, product certification, role of the product certification authority
4. ISO 9000 and ISO 10000 series standards and quality documentation, EN ISO 9001 standard contents and application
5. Quality assurance at the pre-process stage – design (FMEA, QFD), identification of processes and links between processes, constant improvement of processes
6. Management of resources (human resources, material resources, information resources, financial resources), quality system measurements and analyses (customer satisfaction assessment, audits)
7. Constant quality system improvements (corrective and preventive actions, management of non-conformances, audits)
8. Statistical methods - statistical process control, statistical acceptance
9. Quality audits as per ISO 19011
Seminars
1. Quality development and care of quality, economy and quality
2. Basic concepts, quality planning, documentation and records
3. QFD, FMEA, DOE
4. Quality documentation development. Quality manual
5. The 7 "basic" quality tools
6. Seven "new" quality tools
7. Control charts
8. Development of an EC Declaration of Conformity
9. Assessment of the program developed