Auditing for Medical Device and Pharma Companies A Tool to Reduce Quality and Compliance Risk 2017 is a seminar that covers topics such as:
- 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
Auditing for Medical Device and Pharma Companies A Tool to Reduce Quality and Compliance Risk 2017 brings together:
- 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
