Introduction to FDA Good Documentation Practices 2012

Introduction to FDA Good Documentation Practices 2012 is a webinar that covers topics such as:

• 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

Introduction to FDA Good Documentation Practices brings together 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.