Article 32(Jurisdiction of Ministry of Agriculture, Food and Rural Affairs) #
(1) The Minister of Agriculture, Food and Rural Affairs shall delegate his or her authority over the following matters to the Special Metropolitan City Mayor, a Metropolitan City Mayor, a Special Self-Governing City Mayor, a Do Governor, or a Special Self-Governing Province Governor, respectively: <Amended on Apr. 20, 2010; Jan. 24, 2011; Apr. 10, 2012; Jan. 16, 2013; Mar. 23, 2013; Mar. 3, 2015; Oct. 31, 2017>
1. Authority under Articles 32, 33, and 36 of the Farmland Expansion and Development Promotion Act (Act No. 2767) and the proviso of paragraph (3) of the Addenda of that Act, which comply with the previous provisions pursuant to Article 5 (1) of the Addenda of the Agricultural and Fishing Villages Improvement Act (Act No. 4823);
2. Consultation on gratuitous transfer and gratuitous reversion to project operators of public facilities under statutes other than the State Property Act with regard to State property for agricultural infrastructure;
3. The following matters regarding State property (limited to State property for agricultural infrastructure defined in subparagraph 6 of Article 2 of the Rearrangement of Agricultural and Fishing Villages Act) under the State Property Act (hereafter in this subparagraph referred to as the "Act") and the Enforcement Decree of that Act (hereafter in this subparagraph referred to as the "Decree"):
(a) Management and disposal of State property under Article 8 (3) of the Act;
(b) Acquisition of real estate without an owner under Article 12 of the Act;
(c) Acceptance of donation under Article 13 of the Act;
(d) Registration of acquired property, transfer of title, and other measures necessary for preservation of rights under Article 14 of the Act;
(e) Consultation on administrative conversion under Article 16 of the Act and transfer of documents, etc. determined to be subject to administrative conversion under Article 11 of the Decree;
(f) Entrustment of the administration of State property under Article 29 of the Act;
(g) Permission and approval for use under Article 30 of the Act;
(h) Collection of usage fees, deposit of bonds, and performance guarantee measures under Article 32 of the Act;
(i) Exemption from usage fees under Article 34 of the Act;
(j) Renewal of permission for use under Article 35 (2) of the Act;
(k) Revocation and withdrawal of permission for use, compensation for losses incurred by withdrawal, and notification of revocation or withdrawal under Article 36 of the Act;
(l) Hearings under Article 37 of the Act;
(m) Sanctions against negligence in management under Article 39 of the Act;
(n) Disuse and transfer of disused property under Article 40 of the Act;
(o) Loans, restrictions on loans, collection of rent, exemption from rent, and cancellation or termination of loan agreements under Articles 46 and 47 of the Act;
(p) Collection of indemnities, overdue charges, etc. under Articles 72 and 73 of the Act, consultation on determination and modification of urban management planning for State Property, and restrictions on use and preservation of State Property requested pursuant to Article 73-2 of the Act;
(q) Removal of illegal facilities under Article 74 of the Act;
(r) Return of overpaid or erroneously-paid amount under Article 75 of the Act;
4. Deleted; <Dec. 31, 2024>
5. Deleted; <Dec. 31, 2024>
6. The following matters under the Fisheries Act (hereafter in this subparagraph referred to as the "Act"):
(a) The authority to consult on the formulation or modification of a fishing ground use and development plan, which shall comply with the previous provisions pursuant to Article 4 (4) and (6) of the Act and paragraph (3) of the Addenda to the Enforcement Decree of the Public Waters Reclamation Act (Presidential Decree No. 19080), among the authority to consult on the formulation or modification of a fishing ground use and development plan under Article 40 (4) of the Enforcement Decree of the Public Waters Reclamation Act (referring to the Enforcement Decree of the Public Waters Reclamation Act before it was amended by Presidential Decree No. 19080), where the head of a Si/Gun/Gu is the project operator;
(b) The authority to consult on the formulation or modification of a fishing ground use and development plan under Article 40 (4) of the Enforcement Decree of the Public Waters Reclamation Act (referring to the Enforcement Decree of the Public Waters Reclamation Act before it was amended by Presidential Decree No. 19080), which shall comply with the previous provisions pursuant to Article 15 (1) of the Act and paragraph (3) of the Addenda to the Enforcement Decree of the Public Waters Reclamation Act (Presidential Decree No. 19080), among the authority to consult on limited fishery business licenses under Article 40 (4) of the Enforcement Decree of the Public Waters Reclamation Act (referring to the Enforcement Decree of the Public Waters Reclamation Act before it was amended by Presidential Decree No. 19080), where the head of a Si/Gun/Gu is the project operator;
7. Permission to incorporate a non-profit corporation under the jurisdiction of the Minister of Agriculture, Food and Rural Affairs (limited to cases where the scope of activities of a corporation is limited to the jurisdiction of the relevant Special Metropolitan City Mayor, Metropolitan City Mayor, Special Self-Governing City Mayor, Do Governor, or Special Self-Governing Province Governor), which is established or to be established pursuant to Article 32 of the Civil Act, and the authority to revoke such permission, to amend its articles of incorporation, to accept reports on dissolution, and to provide guidance and supervision;
8. The following matters concerning important property acquired with subsidies granted to the Special Metropolitan City Mayor, a Metropolitan City Mayor, a Special Self-Governing City Mayor, a Do Governor, or a Special Self-Governing Province Governor pursuant to the Subsidy Management Act (hereafter in this subparagraph referred to as the "Act") or important property whose utility has increased:
(a) Approval for the use, transfer, exchange, lease, or provision of security of any important property for any purpose other than the originally intended purpose under the main clause of Article 35 (3) of the Act, and issuance of an order to return the amount under the subparagraphs of paragraph (4) of that Article;
(b) Business affairs regarding verifying the return of all indirect subsidies under Article 35-2 (4) 1 of the Act;
9. Deleted; <Mar. 23, 2013>
10. Deleted. <Jan. 28, 2014>
(2) The Minister of Agriculture, Food and Rural Affairs shall delegate his or her authority concerning the following matters to the Administrator of the Rural Development Administration: <Added on Mar. 3, 2015>
1. Determination of standard required quantity of raw materials for agricultural pesticide for export among authority under Article 91 (1) 2 of the Enforcement Decree of the Foreign Trade Act;
2. Deleted. <Nov. 30, 2015>
(3) Deleted. <Nov. 30, 2015>
(4) Pursuant to Article 85 of the Pharmaceutical Affairs Act and Article 46 of the Medical Devices Act, the Minister of Agriculture, Food and Rural Affairs shall delegate his or her authority concerning the following matters, which shall be used only for animals, to the Commissioner of the Animal and Plant Quarantine Agency; provided, the authority concerning use only for aquatic animals under the jurisdiction of the Minister of Oceans and Fisheries pursuant to Article 85 of the Pharmaceutical Affairs Act shall be excluded herefrom: <Amended on Jun. 7, 2011; Mar. 23, 2013; Oct. 31, 2017>
1. The following matters under the Pharmaceutical Affairs Act (hereafter in this subparagraph referred to as the "Act"):
(a) Permission for manufacturing business of drugs, reporting on contract manufacturing and distribution business of drugs, reporting on manufacturing business of quasi-drugs, acceptance of permission by item or reporting on manufacturing business of quasi-drugs, modification of permitted matters or reported matters, and receipt of data on safety and effectiveness under Article 31 (1) through (4), (9), and (10) of the Act; provided, the acceptance of reports by item and reports on modification for items which the Minister of Agriculture, Food and Rural Affairs recognizes as having no problems with safety or effectiveness shall be excluded;
(b) Reexamination of new drugs, etc. under Article 32 (1) of the Act;
(c) Re-evaluation of drugs under Article 33 (1) of the Act;
(d) Approval of a clinical trial protocol for drugs, etc., restrictions on clinical trials, prohibition of use of drugs, etc. for clinical trials, and measures such as recall and destruction under Article 34 (1), (5), and (6) of the Act;
(e) Acceptance of reports on the designation of institutions conducting clinical trials and institutions conducting bioequivalence tests, designation of modifications thereof, revocation of designation thereof, and suspension of business affairs under Articles 34-2 (1) and (2) and 76-2 (1) of the Act;
(f) Acceptance of reports on the designation of institutions conducting non-clinical studies, designation of modification thereof, revocation of designation thereof, and suspension of business of institutions conducting non-clinical studies under Articles 34-3 (1) and (2) and 76-2 (1) of the Act;
(g) Conditional permission and revocation thereof under Article 35 of the Act;
(h) Approval for a physician, specialized technician, or technician to be assigned pursuant to the proviso of Article 36 (1), paragraph (2) of that Article, and Article 42 (4) of the Act;
(i) Training orders for manufacturing managers and the designation and public notification of institution offering education for manufacturing managers under Article 37-2 (2) and (4) of the Act;
(j) Education orders for persons in charge of safety management of drugs and designation of educational institutions for persons in charge of safety management of drugs under Article 37-4 (2) and (4) of the Act;
(k) Acceptance of reports on the production performance, etc. of manufacturers and importers of drugs, etc. under Articles 38 (2) and 42 (4) of the Act;
(l) Acceptance of reports on a plan for recall of drugs, etc. in distribution which have problems with safety and effectiveness under Article 39 (1) of the Act;
(m) Acceptance of reports on temporary or permanent closure of business, etc., which are filed by a manufacturer of drugs, etc. or a person who has obtained permission by item of drugs, etc. under Article 40 of the Act;
(n) Acceptance of a report on import business of drugs, etc.; permission for, or acceptance of a report on, imported items; or modification of permitted matters or reported matters under Article 42 (1) of the Act; provided, the acceptance of a declaration by item and a declaration for modification thereof for items which the Minister of Agriculture, Food and Rural Affairs recognizes as having no problems with safety and effectiveness shall be excluded;
(o) Permission to export or import drugs or to bring them into Korea through international waters, among products processed from animals and plants under the Convention on International Trade in Endangered Species of Wild Fauna and Flora under Article 43 (1) of the Act;
(p) Formulation of necessary standards, such as the nature, condition, quality, and storage methods of drugs, etc. under Article 52 of the Act;
(q) Approval for shipment of drugs under Article 53 (1) of the Act;
(r) Consultation on matters necessary for the manufacture, import, etc. of radioactive drugs under Article 54 of the Act;
(s) Designation of tar pigments under subparagraph 7 of Article 62 of the Act;
(t) Deliberation on advertisement of drugs under Article 68-2 (1) of the Act;
(u) Instructions under the subparagraphs of Article 69 (1) of the Act;
(v) Orders for production and orders for commencement of business under Article 70 (1) of the Act;
(w) Issuing an order to recall or destroy, or issuing an order to take other necessary measures and making dispositions under Article 71 (1) through (3) of the Act;
(x) Orders to publish a plan for recall of drugs, etc. and measures such as recall and destruction under Article 72 (1) and (2) of the Act;
(y) Ordering manufacturers and importers of drugs, etc. to receive inspections under Article 73 of the Act;
(z) Ordering manufacturers of drugs, etc., persons who have obtained permission by item of drugs, or importers to repair facilities and to suspend use of facilities, etc. under Article 74 of the Act;
(aa) Ordering manufacturers of drugs, etc. under Article 75 of the Act and importers for whom that Article is applied mutatis mutandis pursuant to Article 42 (4) of that Act to change their managers;
(ab) Revocation of permission, approval, or registration, prohibition of the manufacture or importation of drugs, or order to suspend business in whole or in part, to a manufacturer of drugs, etc., a person who has obtained permission by item, or an importer under Article 76 of the Act;
(ac) Hearings on the revocation of the designation of a manufacturer of drugs, etc., a person who has obtained permission by item, an importer, an institution conducting clinical trials, an institution conducting bioequivalence tests, or an institution conducting non-clinical studies under Article 77 of the Act;
(ad) Appointment of pharmaceutical inspectors in connection with drugs, etc. under Article 78 (2) of the Act;
(ae) Imposition and collection of penalty surcharges on manufacturers of drugs, etc., persons who have obtained permission by item, or importers of drugs, etc. under Article 81 of the Act;
(af) Establishment of standards for use of drugs under Article 85 (2) of the Act;
(ag) Imposing or collecting administrative fines on or from manufacturers of drugs, etc., persons who have obtained permission by item, or importers of drugs, etc. under Article 98 of the Act;
2. The following matters under the Medical Devices Act (hereafter in this subparagraph referred to as the "Act"):
(a) Classification and designation of medical devices under Article 3 (1) of the Act;
(b) Acceptance of a manufacturing business permission for medical devices, manufacturing permission by item, or manufacturing report by item under Article 6 of the Act, and permission for alteration or report on alteration under Article 12 of that Act; provided, the acceptance of the report on manufacturing by item or the report on modification for items which the Minister of Agriculture, Food and Rural Affairs recognizes as having no problems with safety and effectiveness shall be excluded;
(c) Acceptance of conditional permission or reports on manufacturing business of medical devices or manufacturing business of medical devices or items under Article 7 of the Act;
(d) Orders for re-examination of newly developed medical devices, etc. and acceptance of applications for re-examination under Article 8 of the Act;
(e) Re-evaluation of medical devices under Article 9 of the Act;
(f) Approval of a clinical trial protocol and approval for modification thereof under Article 10 (1) of the Act, modification and revocation of clinical trials under paragraph (4) of that Article, and other necessary measures;
(g) Designation, revocation of designation, and suspension of business of clinical trial institutions under Articles 10 (3) and 37 (1) of the Act;
(h) Designation of institutions conducting non-clinical trials, modification of designation, revocation of designation, and suspension of business of institutions conducting non-clinical trials under Articles 10-2 (1) and 37 (1) of the Act;
(i) Acceptance of reports on the production performance, etc. of the manufacturers of medical devices under Article 13 (2) of the Act;
(j) Acceptance of reports on temporary or permanent closure of business, etc. by manufacturers or importers of medical devices under Articles 14 and 15 (6) of the Act;
(k) Permission for the import business of medical devices under Article 15 of the Act, acceptance of import permission by item or import declaration by item, and permission to change or report on change; provided, the acceptance of import declarations by item and the report on alteration of the import declaration by item for items which the Minister of Agriculture, Food and Rural Affairs recognizes as having no problems with safety and effectiveness shall be excluded;
(l) Acceptance of reports on medical device repair business under Article 16 of the Act;
(m) Formulation of standard specifications for the scope of application, etc. of medical devices under Article 19 of the Act;
(n) Designation of matters stated in package inserts under subparagraph 3 of Article 22 of the Act;
(o) Deliberation on advertisements under Article 25 of the Act;
(p) Receipt of reports on side effects of medical devices under Article 31 (1) of the Act;
(q) Orders to report medical devices and visits, inspections, inquiries, and collection of medical devices under Article 32 (1) of the Act;
(r) Orders to inspect medical devices under Article 33 of the Act;
(s) Issuing orders to destruct hazardous medical devices under Article 34 of the Act;
(t) Issuing orders to suspend use of medical devices under Article 35 of the Act;
(u) Revocation of permission for manufacturers, importers, and repairers of medical devices, closure of places of business, prohibition of manufacturing, importing, and distributing items, and suspension of business of manufacturers, importers, and repairers of medical devices under Article 36 (1) of the Act;
(v) Imposing or collecting penalty surcharges on or from medical device handlers under Article 38 of the Act;
(w) Hearings on the revocation of designation of medical device handlers, institutions conducting clinical trials, or institutions conducting non-clinical trials under Article 39 of the Act;
(x) Appointment of medical device surveillance officers under Article 40 (2) of the Act;
(y) Imposing or collecting administrative fines on or from manufacturers, importers, and repairers of medical devices under Article 56 of the Act.
(5) The Minister of Agriculture, Food and Rural Affairs shall, among the duties concerning the operation and management of the Fund under Article 56 (3) of the Act on the Distribution and Price Stabilization of Agricultural and Fishery Products, delegate his or her authority over the revenue and expenditure of the Fund and the acquisition, operation, disposal, etc. of the Fund's property related to the seed business, etc. to the Director General of the Korea Seed and Variety Service. <Amended on Mar. 3, 2015>
(6) Deleted. <Mar. 3, 2015>
(7) Deleted. <Mar. 3, 2015>
(8) The Minister of Agriculture, Food and Rural Affairs shall delegate the authority on the following matters to the Commissioner of the Animal and Plant Quarantine Agency, the Director General of the National Agricultural Products Quality Management Service, the Director of the Food and Agriculture Officials Training Institute, the President of the Korea National University of Agriculture and Fisheries, and the Director of the Korea Seed and Variety Service, respectively, depending on their jurisdiction: <Amended on Jun. 7, 2011; Mar. 23, 2013; May 31, 2022>
1. Consultation on gratuitous transfer and gratuitous reversion to project operators of public facilities under statutes other than the State Property Act;
2. Restrictions on qualifications for participation by inappropriate business entities in tendering procedures and notification thereof under Article 27 (1) of the Act on Contracts to Which the State Is a Party.
(9) Deleted. <Mar. 23, 2013>
(10) Deleted. <Mar. 23, 2013>
(11) The Minister of Agriculture, Food and Rural Affairs shall delegate his or her authority over the following matters under the Agricultural and Fishery Products Quality Control Act (hereafter in this paragraph referred to as the "Act") entrusted by the Minister of Food and Drug Safety pursuant to Article 18 (4) to the Director General of the National Agricultural Products Quality Management Service: <Added on Mar. 23, 2013>
1. Safety inspection of agricultural products under Article 61 of the Act;
2. Collection, investigation, and inspection of samples of agricultural products under Article 62 of the Act;
3. Taking measures based on results of safety inspections of agricultural products and notifying the results thereof pursuant to Article 63 of the Act;
4. Designation of safety inspection agencies for agricultural products under Article 64 of the Act;
5. Dispositions, such as revocation of designation of safety inspection agencies for agricultural products under Article 65 of the Act;
6. Education and public relations on the safety of agricultural products, entrustment of education and public relations, and budgetary support for education and public relations on the safety of agricultural products under Article 66 of the Act;
7. Research, development, and dissemination of technology for safety analysis methods, etc. of agricultural products under Article 67 of the Act;
8. Reduction of, exemption from, and collection of fees for applying for the designation of safety inspection agencies for agricultural products under subparagraph 10 of Article 113 of the Act;
9. Hearings under Article 114 (1) 9 of the Act.
(12) The Minister of Agriculture, Food and Rural Affairs shall delegate the following matters (limited to matters concerning slaughterhouses, milk collection stations, or farms) entrusted by the Minister of Food and Drug Safety pursuant to the proviso of Article 44 (2) of the Livestock Products Sanitary Control Act (hereafter in this paragraph referred to as the "Act") and Article 31 (5) of the Enforcement Decree of that Act to the Commissioner of the Animal and Plant Quarantine Agency: <Added on Mar. 23, 2013; Jan. 28, 2014; Jan. 17, 2017; Nov. 24, 2020>
1. Provision of technology and information necessary for compliance with HACCP and provision of education and training under Article 9 (10) of the Act;
1-2. Examining, evaluating, and providing support for individual HACCP and the appropriateness of their operation under Article 9-3 (2) and (4) of the Act;
2. Access to and inspection of workplaces or farms for verifying the appropriateness of HACCP under Article 9-3 (6) of the Act;
3. Revocation of HACCP-accredited place of work, etc. and issuance of corrective orders under Article 9-4 of the Act;
4. Supervision over the business of the Korea Agency of HACCP Accreditation and Service under the Act on the Establishment and Operation of the Korea Agency of HACCP Accreditation and Service (limited to business under subparagraph 2 of Article 6 of that Act);
5. Appointment of an inspector who is a public official belonging to the Animal and Plant Quarantine Agency in charge of inspecting slaughterhouses and milk collection stations under Article 13 (1) of the Act;
6. Issuance of an order to a slaughterhouse business operator or milk collection business operator to report the results of inspection of livestock products and an order for an inspector to inspect a slaughterhouse or milk collection station and to collect livestock products under Article 19 (1) of the Act;
7. Issuance of an order for an inspector to seize or destroy livestock products pursuant to Article 36 of the Act;
8. Payment of monetary awards under Article 39 of the Act (payment shall be limited to those who report, accuse, or arrest a person who has committed a violation related to the slaughter, processing, and collection of milk or who has committed an improper act against livestock, and those who cooperate in the arrest);
9. Hearings under subparagraph 1 of Article 43 of the Act.
[Title Amended on Mar. 23, 2013]