Auditing for Medical Device and Pharma Companies – A Tool to Reduce Quality and Compliance Risk 2017

Topics

• How to develop and implement an efficient and effective audit program
• Regulatory Expectations
• Red-flags that your program is not effective
• Common problems
• Audit Program Structure
• Risk Analysis techniques
• Documentation and communication
• The auditing process – steps and tools
• Linkages within your Quality System to ensure audits lead to effective solutions and lasting improvement

Who should Attend

• Document Control Specialists
• Quality Systems Specialists
• Auditors
• Quality and Compliance Specialists
• Supplier Auditors
• Internal Auditors
• Supplier Auditors
• Auditor Managers
• Quality/Compliance managers or directors for Medical Device, Pharmaceutical, or Bio-tech companies
• CAPA Specialists