Webinar On FDA proposed changes to ISO 13485: 2015 and Medical Devices Quality Management Systems
January 30, 2015 - Mississauga ON CACompliance Trainings
suzzane.d@compliancetrainings.com
Phone:4169154458
The webinar will also focus on the major difference in expectations between FDA Quality System Regulations and Quality System inspection Techniques (QSR and QSIT) and ISO 13485 for globally distributed products. Proposed changes to ISO 13485 for additional vigilance in areas such as supplier management, risk management and training will be discussed. Areas Covered in the Session : You will gain a thorough understanding of: Requirements of ISO 13485 How to carefully attend to every aspect of the related biomedical standards Document control Purchasing Controls Production controls CAPA Identification and Traceability Upcoming changes ISO 13485:2015 How ISO 13485 differ from FDA QSR 21 CFR 820 requirements Regulatory expectations of other major growing geographies in the world Who Will Benefit: A must attend webinar for Managers, Supervisors, Leads, Specialists, Engineers and Groups in Department of: Quality Assurance Regulatory Affairs Research & Development Quality Control Supplier Management Documentation Production Internal Auditors Quality Auditors Supplier Auditors Operations Manufacturing Suppliers to medical device industry Price tags: Live Single Live : For One Participant $ 249 Corporate Live : For Max. 10 Participants $ 899 Recording Single REC : For One Participant - Unlimited Access for 6 Months $ 299 For more information and enquiries contact us at Compliance Trainings 5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada Customer Support : #416-915-4458 Email : support@compliancetrainings.com