Training Program on ISO 13485: 2016 standards, Manufacturing Standards for Medical Devices, Audit Process.
Eligibility: Any (working professional & interested students)
Nationality: Any
Duration: 3 Days - (8th , 9th , 10th January 2025) - (Time: 10:00 AM - 5:00 PM)
Course Outcomes:
· Use of ISO 13485:2016 as the basis for a QMS for medical device manufacturers
2 Ways to increase effective manufacturing of medical devices and cost savings through quality management
· Supply chain monitoring to achieve continuous improvement
· Understanding how to meet regulatory requirements leading to increased patient safety
· Certificate will be provided to each participant upon successful completion of the assessment