Contents
- Part I General
- Part II Releasing organisms for any other purpose than marketing
- Part III Marketing organisms
- Part IV Duties after the making of applications
- Part V General provisions for consents
- Part VI Safeguard
- Part VII Confidentiality
- Part VIII Register of information
- Part IX Miscellaneous
- Schedule 1 Information to be included in applications for consent to release genetically modified higher plants for non-marketing purposes
- SCHEDULE1A Information to be included in applications for consent to market genetically modified higher plants
- Schedule 2 Information to be included in applications for consent to release or market organisms other than genetically modified higher plants
- Schedule 3 Information to be included in applications for consent to market genetically modified organisms
- SCHEDULE3A Information to be provided to the Secretary of State alongside a notice of intention to release a qualifying higher plant
- Schedule 4 Information to be included in an assessment report
- Schedule 5 Revocations
Contents
675 provisions, too many to show on one page. Open a part or section to read it with its history and connections, or search inside the text.
- Part I · General
- 1 Citation, commencement, extent and application
- 2 Interpretation
- 3 Purpose of Part VI of the Act and meaning of “genetically modified organisms” etc
- 4 Meaning of “damage to the environment” etc
- 5 Techniques of genetic modification
- 6 Environmental risk assessment
- 7 Communication with applicant for consent
- Part II · Releasing organisms for any other purpose than marketing
- 8 Requirement for consent to release
- 9 Exempt Activities
- 9A Exemption for release of qualifying higher plants
- 9B Notification requirement for release of qualifying higher plants
- 10 Applications for consent to release—general provisions
- 11 Information to be contained in applications for consent to release
- 12 Advertisement of applications for consent to release
- 13 Transitional provisions for release
- Part III · Marketing organisms
- 14 Requirement for consent to market
- 15 Exempt activities
- 16 Applications for consent to market
- 17 Transitional provisions for marketing
- 17A Transitional measures for adventitious or technically unavoidable presence of genetically modified material which has benefited from a favourable risk evaluation.
- 18 Applications for renewal of consent to market
- Part IV · Duties after the making of applications
- 19 Duty of the applicant after applying for consent to release or to market
- 20 Duties of the Secretary of State in relation to applications for consent to release
- 21 Decisions by the Secretary of State on applications for consent to release
- 22 Variation or revocation of consents to release
- 23 Duties of the Secretary of State in relation to applications for consent to market
- 24 Decisions by the Secretary of State on applications for consent to market
- 25 Duties of the Secretary of State on receiving applications for renewal of consent to market
- 26 Decisions by the Secretary of State on applications for renewal of consent to market
- 27 Genetically modified organisms containing antibiotic resistance markers
- Part V · General provisions for consents
- Part VI · Safeguard
- Part VII · Confidentiality
- Part VIII · Register of information
- Part IX · Miscellaneous
- Schedule 1 · Information to be included in applications for consent to release genetically modified higher plants for non-marketing purposes
- Part 4A Information on specific areas of risk
- Part I General Information
- Part II Information relating to the parental or recipient plant
- Part III Information relating to the genetic modification
- Part IV Information relating to the genetically modified plant
- Part V Information relating to the site of release
- Part VI Information relating to the release
- Part VII Information on control, monitoring, post-release and waste treatment plans
- Part VIII Information on methodology
- SCHEDULE1A · Information to be included in applications for consent to market genetically modified higher plants
- PART1 General information
- PART2 Information relating to the parental or recipient plant
- PART3 Information Relating to the Genetic Modification
- PART4 Information relating to the genetically modified plant
- PART5 Information on specific areas of risk
- PART6 Information about the detection, identification and previous releases of the genetically modified plant
- Schedule 2 · Information to be included in applications for consent to release or market organisms other than genetically modified higher plants
- Part I General information
- Part II Information relating to the organisms
- Part III Information relating to the conditions of release
- Part IV Information relating to the interactions between the organisms and the environment
- Part V Information on monitoring, control, waste treatment and emergency response plans
- Part VI Information on methodology
- Schedule 3 · Information to be included in applications for consent to market genetically modified organisms
- SCHEDULE3A · Information to be provided to the Secretary of State alongside a notice of intention to release a qualifying higher plant
- (1) The title of the project under which the qualifying higher...
- (2) The aim of the project (including any matters being investigated...
- (3) The name, address, telephone number and email address of the...
- (4) The name, qualifications and experience of every person responsible for...
- (5) The name, qualifications and experience of every person responsible for...
- (6) The full name of the qualifying higher plant to be...
- (7) The expected date on which the project will start.
- (8) The expected duration of the project.
- Schedule 4 · Information to be included in an assessment report
- (1) An identification of the characteristics of the recipient organism which...
- (2) A description of the way in which the characteristics of...
- (3) An identification of any known risks of damage to the...
- (4) An assessment of whether the genetic modification has been characterised...
- (5) An identification of any new risks of damage to the...
- (6) A conclusion which addresses the proposed use of the product,...
- Schedule 5 · Revocations