Topics
- How and when to apply Good Documentation Practices
- What are Good Documentation Practices?
- How to attach raw data to forms and lab notebooks
- How to complete documentation such as data collection forms and batch records
- How to sign, date and label data and records
- How to correct errors and ommissions in data entry
Who should Attend
Laboratory staff, FDA-regulated biotech, pharma and medical device operations, Engineering and manufacturing associates, Clinical research associates, Regulatory submission associates, Validation engineers, Document control and records associate and Quality personnel.
