FDA and EMA Global Labeling Challenges and Requirements 2019 is a webinar that covers topics such as:
- Complying with FDA and EMA requirements for labeling
- Product labeling background and rationale
- The essential labeling materials that are covered
- Converting Word documents into XML and SPL format
- Inspection of labeling records
- Organizing and maintaining labeling records efficiently and effectively
FDA and EMA Global Labeling Challenges and Requirements 2019 is intended for:
- Manufacturing and Quality Assurance professionals responsible for labeling content, format and management
- Those responsible for designing, creating and maintaining product labels and labeling records
- Quality Assurance Personnel
- IT professionals involved in the conversion of label content formats for electronic labels
- Consultants working in the life sciences industries responsible for assisting companies with FDA and EMA compliance for labeling content, format and management
- Auditors engaged in the internal inspection of labeling records and practices
- All pharmaceutical, biotechnology, medical device and tobacco companies that are regulated by the FDA or an international equivalent agency
