Chapter 1 |
3. Application for authorisation
4. Suspension or withdrawal of authorisation
5. Keeping of records and reporting obligations
7. Stem cells for later therapeutic use
8. Additional powers and duties of an inspector of anatomy or investigating officer
9. Inspection and control measures
11. Data protection and confidentiality
12. Quality and safety of stem cells
17. Stem cell storage conditions
18. Labelling, documentation and packaging
20. Relationship between stem cell establishments and third parties