| PART I |
| General |
| 1. | Citation and commencement. |
| 2. | Interpretation. |
| 3. | Artificial techniques of genetic modification. |
| 4. | Capacity of organisms for causing harm. |
| PART II |
| Releasing organisms |
| 5. | Consent to release organisms. |
| 6. | Information to be contained in application for consent to release. |
| 7. | Exemptions from regulation 6. |
| 8. | Advertisement of application for consent to release. |
| 9. | General condition on consents to release organisms. |
| PART III |
| Marketing organisms |
| 10. | Consent to market products. |
| 11. | Information to be contained in application for consent to market. |
| 12. | Transitional provision for marketing. |
| PART IV |
| Duties after the making of applications |
| 13. | Duty of the applicant after applying for consent. |
| 14. | Duties of the Secretary of State on receiving applications for consent to release. |
| 15. | Decisions by the Secretary of State on applications for consent to release. |
| 16. | Duties of the Secretary of State in relation to applications for consent to market. |
| PART V |
| Register of Information |
| 17. | Information to be included in register. |
| 18. | Keeping of the register. |
