Based on the FDA data, any of these things (except the last) might be the result of poor, ineffective or confusing SOPs. If you can relate to any of these problems, this webinar is for you. Using this acronym as our guide, this webinar will help you:
Learning Objectives:
- Be able to explain the critical purpose of SOPs,
- Be able to describe the current state of their industry’s SOPs (from FDA inspection data).
- Be able to evaluate the usability of their SOPs.
- Begin to write user friendly SOPs that have the proper level of detail.
- Learn tips and tools to simplify and improve their SOPs.
Who Should Attend
- Quality Assurance/Quality Control Directors
- Managers
- Specialists
- Regulatory Affairs/Regulatory Compliance Directors
- Managers and Specialists
- SOP authors
- batch record authors
- reviewers and approvers
