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Conference on Internal Auditing for the Medical Device Industry – GlobalCompliancePanel
June 30, 2016 - July 1, 2016$1,495
This course provides an overview of internal auditing requirements and techniques for medical device companies as a method for risk management and quality improvement.
The course will cover auditing requirements, audit planning, preparation, knowledge, auditor skills, interviews, documents and records review, objective evidence, audit report writing and corrective action.
Why should you attend:
Attendees should attend this seminar for risk management and improvement purposes to identify weaknesses, problems, compliance risks, and improvement opportunities.
Who will benefit:
- Quality Manager
- Quality Associate
- Quality Engineer
- Quality Technician
- Regulatory Associate