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 - (5th, 6th & 7th December 2024) - (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
| S.No | Start Date | End Date | Total Amount (INDIA) | Total Amount (Foriegn) |
|---|---|---|---|---|
| 1 | 2024-11-01 | 2024-12-31 | 10,000 | 17,000 |
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