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Medical Care Act

医療法(いりょうほう)

Chapter V Ensuring the Medical Care Delivery System (Articles 36 to 38-7)

The law as Act Partially Amending the Medical Care Act, etc. (Act No. 87 of 2025) leaves it, with the words it changes marked.

The main text is read a page at a time: a chapter to a page, and a long chapter in runs of articles. The whole main text, and the supplementary provisions and appended tables this amendment changes. Those it leaves untouched are on the page for the text in force.

Section 7 Securing the Supply of Pharmaceuticals to Provide Appropriate Medical Care第七節 適切な医療を提供するための医薬品の供給の確保

Article 36第三十六条

Article 36, paragraph (1)

When the Minister of Health, Labour and Welfare finds that the supply of a specified pharmaceutical (meaning a specified pharmaceutical prescribed in Article 2, paragraph (17) of the Act on Securing Quality, Efficacy and Safety of Products Including Pharmaceuticals and Medical Devices; the same applies hereinafter) is in shortage, or is likely to be in shortage as reasonably judged from the state of supply and demand of the specified pharmaceutical and other circumstances, and that, as a result, the provision of appropriate medical care will become difficult, which may affect the lives and health of the people, the Minister may request marketing authorization holders (meaning persons who have obtained a license for the business of marketing pharmaceuticals under Article 12, paragraph (1) of that Act; the same applies hereinafter), manufacturers (meaning persons who have obtained a license for the business of manufacturing pharmaceuticals under Article 13, paragraph (1) of that Act; the same applies hereinafter), wholesale distributors (meaning persons who have obtained a license for the wholesale distribution business under Article 34, paragraph (1) of that Act; the same applies in Article 38-4) and other related parties to provide the cooperation necessary to ensure the provision of that specified pharmaceutical or an alternative pharmaceutical (meaning an alternative pharmaceutical prescribed in Article 18-5 of that Act; the same applies hereinafter in this Article) to medical institutions that need it, such as increasing the production of, and adjusting the sale of, that specified pharmaceutical or alternative pharmaceutical.

厚生労働大臣は、特定医薬品(医薬品、医療機器等の品質、有効性及び安全性の確保等に関する法律第二条第十七項に規定する特定医薬品をいう。以下同じ。)について、その供給が不足し、又はその特定医薬品の需給の状況その他の状況から合理的に判断して、その供給が不足する蓋然性があると認められるため、適切な医療の提供が困難になることにより、国民の生命及び健康に影響を与えるおそれがあると認める場合は、製造販売業者(同法第十二条第一項の医薬品の製造販売業の許可を受けた者をいう。以下同じ。)、製造業者(同法第十三条第一項の医薬品の製造業の許可を受けた者をいう。以下同じ。)、卸売販売業者(同法第三十四条第一項の卸売販売業の許可を受けた者をいう。第三十八条の四において同じ。)その他の関係者に対し、当該特定医薬品又は代替薬(同法第十八条の五に規定する代替薬をいう。以下この条において同じ。)の増産、販売の調整その他の当該特定医薬品又は代替薬を必要とする医療提供施設に対する当該特定医薬品又は代替薬の提供を図るために必要な協力を求めることができる。

Article 36, paragraph (2)

In the case prescribed in the preceding paragraph, the Minister of Health, Labour and Welfare may request pharmacy establishers (meaning pharmacy establishers prescribed in Article 1-4 of the Act on Securing Quality, Efficacy and Safety of Products Including Pharmaceuticals and Medical Devices), the establishers of hospitals or clinics, and other related parties to provide the cooperation necessary to ensure the provision of medical care to persons who need that specified pharmaceutical or alternative pharmaceutical, such as consideration in dispensing or prescription.

厚生労働大臣は、前項に規定する場合には、薬局開設者(医薬品、医療機器等の品質、有効性及び安全性の確保等に関する法律第一条の四に規定する薬局開設者をいう。)又は病院若しくは診療所の開設者その他の関係者に対し、調剤又は処方に関する配慮その他の当該特定医薬品又は代替薬を必要とする者に対する医療の提供を図るために必要な協力を求めることができる。

Article 37第三十七条

Article 37, paragraph (1)

The Minister of Health, Labour and Welfare is to establish guidelines for securing the stable supply of supply security pharmaceuticals and the raw materials or materials recognized as indispensable for their manufacture (hereinafter referred to as "supply security pharmaceuticals, etc.") (hereinafter referred to as the "guidelines for securing stable supply").

厚生労働大臣は、供給確保医薬品及びその製造に必要不可欠であると認められる原料又は材料(以下「供給確保医薬品等」という。)の安定的な供給の確保を図るための指針(以下「安定供給確保指針」という。)を定めるものとする。

Article 37, paragraph (2)

The guidelines for securing stable supply are to prescribe the following particulars:

安定供給確保指針においては、次に掲げる事項を定めるものとする。

Article 37, paragraph (2), item (i)

the basic direction concerning securing the stable supply of supply security pharmaceuticals, etc.;

供給確保医薬品等の安定的な供給の確保に関する基本的な方向

Article 37, paragraph (2), item (ii)

particulars concerning measures to prevent the occurrence of supply shortages of supply security pharmaceuticals, etc.;

供給確保医薬品等の供給不足の発生を未然に防止するための施策に関する事項

Article 37, paragraph (2), item (iii)

particulars concerning manufacture or importation in the case where a supply shortage of supply security pharmaceuticals, etc. occurs; and

供給確保医薬品等の供給不足が発生した場合における製造又は輸入に関する事項

Article 37, paragraph (2), item (iv)

other important particulars concerning securing the stable supply of supply security pharmaceuticals, etc.

その他供給確保医薬品等の安定的な供給の確保に関する重要事項

Article 37, paragraph (3)

When the Minister of Health, Labour and Welfare has established or amended the guidelines for securing stable supply, the Minister is to publish them without delay.

厚生労働大臣は、安定供給確保指針を定め、又はこれを変更したときは、遅滞なく、これを公表するものとする。

Article 37, paragraph (4)

"Supply security pharmaceutical" in paragraph (1) means a specified pharmaceutical that the Minister of Health, Labour and Welfare, after hearing the Health Sciences Council, designates as having a high necessity of securing its stable supply, in consideration of the following particulars:

第一項の「供給確保医薬品」とは、特定医薬品であつて、次に掲げる事項を勘案し、その安定的な供給の確保を図る必要性が高いものとして、厚生労働大臣が厚生科学審議会の意見を聴いて指定するものをいう。

Article 37, paragraph (4), item (i)

the degree of severity of the symptoms in the case of contracting the disease for which it is used;

その用途に係る疾病にかかつた場合の病状の程度

Article 37, paragraph (4), item (ii)

the existence or non-existence of a specified pharmaceutical or treatment method that can substitute for the specified pharmaceutical;

当該特定医薬品と代替性のある特定医薬品又は治療方法の有無

Article 37, paragraph (4), item (iii)

the existence or non-existence of special technology required for its manufacture, the supply situation of raw materials or materials, and other particulars to be noted regarding its manufacture or supply; and

その製造に要する特別の技術の有無、原料又は材料の供給事情その他の製造又は供給に関して留意すべき事項

Article 37, paragraph (4), item (iv)

other particulars specified by an Order of the Ministry of Health, Labour and Welfare.

その他厚生労働省令で定める事項

Article 38第三十八条

Article 38, paragraph (1)

When the Minister of Health, Labour and Welfare finds, as reasonably judged from the state of manufacture and other circumstances, that there is a likelihood that the supply of important supply security pharmaceuticals (meaning, among the supply security pharmaceuticals prescribed in paragraph (4) of the preceding Article, those that the Minister of Health, Labour and Welfare, after hearing the Health Sciences Council, designates as being particularly important to secure the stable supply of, in consideration of the particulars listed in the items of that paragraph) and the raw materials or materials recognized as indispensable for their manufacture (hereinafter referred to as "important supply security pharmaceuticals, etc.") will be in shortage, and that, if the supply were to be in shortage, the provision of appropriate medical care would become difficult, which may seriously affect the lives and health of the people, the Minister may instruct the marketing authorization holders or manufacturers of the important supply security pharmaceuticals, etc. to prepare, in line with the guidelines for securing stable supply and as provided by Order of the Ministry of Health, Labour and Welfare, a plan concerning the measures necessary to prevent the occurrence of a supply shortage of the important supply security pharmaceuticals, etc. (hereinafter referred to as a "plan for measures to prevent supply shortages" in this Article) and to notify the Minister of Health, Labour and Welfare of it.

厚生労働大臣は、重要供給確保医薬品(前条第四項に規定する供給確保医薬品のうち、同項各号に掲げる事項を勘案し、その安定的な供給の確保を図ることが特に重要なものとして、厚生労働大臣が厚生科学審議会の意見を聴いて指定するものをいう。)及びその製造に必要不可欠であると認められる原料又は材料(以下「重要供給確保医薬品等」という。)について、製造の状況その他の状況から合理的に判断して、その供給が不足する蓋然性があり、かつ、その供給が不足した場合には、適切な医療の提供が困難になることにより、国民の生命及び健康に重大な影響を与えるおそれがあると認めるときは、当該重要供給確保医薬品等の製造販売業者又は製造業者に対し、安定供給確保指針に即して、厚生労働省令で定めるところにより、当該重要供給確保医薬品等の供給不足の発生を未然に防止するために必要な措置に関する計画(以下この条において「供給不足防止措置計画」という。)を作成し、厚生労働大臣に届け出るべきことを指示することができる。

Article 38, paragraph (2)

When the Minister of Health, Labour and Welfare finds it particularly necessary to deal with the situation prescribed in the preceding paragraph, the Minister may instruct a marketing authorization holder or manufacturer that has made a notification in compliance with an instruction under that paragraph, in line with the guidelines for securing stable supply, to change the plan for measures to prevent supply shortages relating to the notification (where a notification of change has been made pursuant to the provisions of the following paragraph, the plan after the change; the same applies hereinafter in this Article) and to notify the Minister of Health, Labour and Welfare of it.

厚生労働大臣は、前項に規定する事態に対処するため特に必要があると認めるときは、同項の規定による指示に従つて届出をした製造販売業者又は製造業者に対し、安定供給確保指針に即して、その届出に係る供給不足防止措置計画(次項の規定による変更の届出があつたときは、その変更後のもの。以下この条において同じ。)を変更し、厚生労働大臣に届け出るべきことを指示することができる。

Article 38, paragraph (3)

A marketing authorization holder or manufacturer that has made a notification in compliance with an instruction under the preceding two paragraphs must, when it has changed the plan for measures to prevent supply shortages relating to the notification, notify the Minister of Health, Labour and Welfare of the changed particulars, as provided by Order of the Ministry of Health, Labour and Welfare.

前二項の規定による指示に従つて届出をした製造販売業者又は製造業者は、その届出に係る供給不足防止措置計画を変更したときは、厚生労働省令で定めるところにより、変更した事項を厚生労働大臣に届け出なければならない。

Article 38, paragraph (4)

A marketing authorization holder or manufacturer that has made a notification in compliance with an instruction under paragraph (1) or (2) must take the measures necessary to prevent the occurrence of a supply shortage of the important supply security pharmaceuticals, etc. relating to the plan for measures to prevent supply shortages, in line with the plan relating to the notification.

第一項又は第二項の規定による指示に従つて届出をした製造販売業者又は製造業者は、その届出に係る供給不足防止措置計画に沿つて当該供給不足防止措置計画に係る重要供給確保医薬品等の供給不足の発生を未然に防止するために必要な措置を行わなければならない。

Article 38, paragraph (5)

When the Minister of Health, Labour and Welfare finds that a marketing authorization holder or manufacturer that received an instruction under paragraph (2) has not complied with the instruction without justifiable grounds, or that a marketing authorization holder or manufacturer prescribed in the preceding paragraph has not, without justifiable grounds, taken the measures necessary to prevent the occurrence of a supply shortage of the important supply security pharmaceuticals, etc. relating to the plan for measures to prevent supply shortages, in line with the plan relating to the notification, the Minister may make public that fact.

厚生労働大臣は、第二項の規定による指示を受けた製造販売業者若しくは製造業者が正当な理由がなくその指示に従わなかつたとき、又は前項に規定する製造販売業者若しくは製造業者が正当な理由がなくその届出に係る供給不足防止措置計画に沿つて当該供給不足防止措置計画に係る重要供給確保医薬品等の供給不足の発生を未然に防止するために必要な措置を行つていないと認めるときは、その旨を公表することができる。

Article 38-2第三十八条の二

Article 38-2, paragraph (1)

When the Minister of Health, Labour and Welfare finds that, due to an increase in demand, a decrease in the quantity manufactured or other circumstances, the supply of important supply security pharmaceuticals, etc. is actually in shortage, or the likelihood of its being in shortage is particularly high as reasonably judged from the state of supply and demand of the important supply security pharmaceuticals, etc. and other circumstances, and that, due to the shortage of supply, the provision of appropriate medical care would become difficult, which may seriously affect the lives and health of the people, the Minister may instruct the marketing authorization holders or manufacturers of the important supply security pharmaceuticals, etc., in line with the guidelines for securing stable supply and as provided by Order of the Ministry of Health, Labour and Welfare, to prepare a plan concerning the manufacture or importation of the important supply security pharmaceuticals, etc. (hereinafter referred to as a "plan for manufacturing, etc." in this Article) and to notify the Minister of Health, Labour and Welfare of it.

厚生労働大臣は、重要供給確保医薬品等について、需要の増加又は製造数量の減少その他の事情により、現にその供給が不足し、又は重要供給確保医薬品等の需給の状況その他の状況から合理的に判断して、その供給が不足する蓋然性が特に高く、かつ、その供給の不足により、適切な医療の提供が困難になり、国民の生命及び健康に重大な影響を与えるおそれがあると認めるときは、当該重要供給確保医薬品等の製造販売業者又は製造業者に対し、安定供給確保指針に即して、厚生労働省令で定めるところにより、当該重要供給確保医薬品等の製造又は輸入に関する計画(以下この条において「製造等計画」という。)を作成し、厚生労働大臣に届け出るべきことを指示することができる。

Article 38-2, paragraph (2)

When the Minister of Health, Labour and Welfare finds it particularly necessary to deal with the situation prescribed in the preceding paragraph, the Minister may instruct a marketing authorization holder or manufacturer that has made a notification in compliance with an instruction under that paragraph, in line with the guidelines for securing stable supply, to change the plan for manufacturing, etc. relating to the notification (where a notification of change has been made pursuant to the provisions of the following paragraph, the plan after the change; the same applies hereinafter in this Article) and to notify the Minister of Health, Labour and Welfare of it.

厚生労働大臣は、前項に規定する事態に対処するため特に必要があると認めるときは、同項の規定による指示に従つて届出をした製造販売業者又は製造業者に対し、安定供給確保指針に即して、その届出に係る製造等計画(次項の規定による変更の届出があつたときは、その変更後のもの。以下この条において同じ。)を変更し、厚生労働大臣に届け出るべきことを指示することができる。

Article 38-2, paragraph (3)

A marketing authorization holder or manufacturer that has made a notification in compliance with an instruction under the preceding two paragraphs must, when it has changed the plan for manufacturing, etc. relating to the notification, notify the Minister of Health, Labour and Welfare of the changed particulars, as provided by Order of the Ministry of Health, Labour and Welfare.

前二項の規定による指示に従つて届出をした製造販売業者又は製造業者は、その届出に係る製造等計画を変更したときは、厚生労働省令で定めるところにより、変更した事項を厚生労働大臣に届け出なければならない。

Article 38-2, paragraph (4)

A marketing authorization holder or manufacturer that has made a notification in compliance with an instruction under paragraph (1) or (2) must manufacture or import the important supply security pharmaceuticals, etc. relating to the plan for manufacturing, etc., in line with the plan relating to the notification.

第一項又は第二項の規定による指示に従つて届出をした製造販売業者又は製造業者は、その届出に係る製造等計画に沿つて当該製造等計画に係る重要供給確保医薬品等の製造又は輸入を行わなければならない。

Article 38-2, paragraph (5)

When the Minister of Health, Labour and Welfare finds that a marketing authorization holder or manufacturer that received an instruction under paragraph (2) has not complied with the instruction without justifiable grounds, or that a marketing authorization holder or manufacturer prescribed in the preceding paragraph has not, without justifiable grounds, manufactured or imported the important supply security pharmaceuticals, etc. relating to the plan for manufacturing, etc., in line with the plan relating to the notification, the Minister may make public that fact.

厚生労働大臣は、第二項の規定による指示を受けた製造販売業者若しくは製造業者が正当な理由がなくその指示に従わなかつたとき、又は前項に規定する製造販売業者若しくは製造業者が正当な理由がなくその届出に係る製造等計画に沿つて当該製造等計画に係る重要供給確保医薬品等の製造若しくは輸入を行つていないと認めるときは、その旨を公表することができる。

Article 38-3第三十八条の三

Article 38-3, paragraph (1)

The national government may take financial and other necessary measures for marketing authorization holders or manufacturers that, in compliance with an instruction under Article 38, paragraph (1) or (2), take the measures necessary to prevent the occurrence of a supply shortage of important supply security pharmaceuticals, etc., and for marketing authorization holders or manufacturers that, in compliance with an instruction under paragraph (1) or (2) of the preceding Article, manufacture or import important supply security pharmaceuticals, etc.

国は、第三十八条第一項又は第二項の規定による指示に従つて重要供給確保医薬品等の供給不足の発生を未然に防止するために必要な措置を行う製造販売業者又は製造業者及び前条第一項又は第二項の規定による指示に従つて重要供給確保医薬品等の製造又は輸入を行う製造販売業者又は製造業者に対し、必要な財政上の措置その他の措置を講ずることができる。

Article 38-4第三十八条の四

Article 38-4, paragraph (1)

A marketing authorization holder, manufacturer or wholesale distributor of supply security pharmaceuticals, etc., or another person specified by Order of the Ministry of Health, Labour and Welfare, must, in line with the guidelines for securing stable supply and as provided by Order of the Ministry of Health, Labour and Welfare, report to the Minister of Health, Labour and Welfare the status of manufacture, importation, sale or provision of supply security pharmaceuticals, etc. and other necessary particulars.

供給確保医薬品等の製造販売業者、製造業者又は卸売販売業者その他厚生労働省令で定める者は、安定供給確保指針に即して、厚生労働省令で定めるところにより、供給確保医薬品等の製造、輸入、販売又は授与の状況その他必要な事項を厚生労働大臣に報告しなければならない。

Article 38-5第三十八条の五

Article 38-5, paragraph (1)

With regard to supply security pharmaceuticals, etc., the Minister of Health, Labour and Welfare may, in line with the guidelines for securing stable supply, request marketing authorization holders or manufacturers and other persons specified by Order of the Ministry of Health, Labour and Welfare to provide the cooperation necessary to prevent the occurrence of a supply shortage of the supply security pharmaceuticals, etc.

厚生労働大臣は、供給確保医薬品等について、製造販売業者又は製造業者その他厚生労働省令で定める者に対し、安定供給確保指針に即して、当該供給確保医薬品等の供給不足の発生を未然に防止するために必要な協力を求めることができる。

Article 38-6第三十八条の六

Article 38-6, paragraph (1)

The Minister of Health, Labour and Welfare may, to the extent necessary for the enforcement of the provisions of Article 38 and Article 38-2, have marketing authorization holders or manufacturers report on the state of their business or accounting, or have the relevant officials enter the business offices, offices and other places of business of these persons and inspect books, documents and other articles.

厚生労働大臣は、第三十八条及び第三十八条の二の規定の施行に必要な限度において、製造販売業者又は製造業者に対し、その業務若しくは経理の状況に関し報告させ、又は当該職員に、これらの者の営業所、事務所その他の事業場に立ち入り、帳簿、書類その他の物件を検査させることができる。

Article 38-6, paragraph (2)

The provisions of Article 6-24, paragraphs (2) and (3) apply mutatis mutandis to the entry and inspection under the provisions of the preceding paragraph.

第六条の二十四第二項及び第三項の規定は、前項の規定による立入検査について準用する。

Article 38-7第三十八条の七

Article 38-7, paragraph (1)

In order to ascertain the state of supply and demand for specified pharmaceuticals, the Minister of Health, Labour and Welfare may conduct surveys and analysis of the information under Article 12-2, paragraph (3) of the Act on Promotion of Comprehensive Securing of Medical and Long-Term Care in Communities and other information specified by Order of the Ministry of Health, Labour and Welfare (referred to as "information on dispensing of pharmaceuticals, etc." in the following paragraph).

厚生労働大臣は、特定医薬品の需給状況を把握するため、地域における医療及び介護の総合的な確保の促進に関する法律第十二条の二第三項の情報その他厚生労働省令で定める情報(次項において「医薬品調剤等情報」という。)について調査及び分析を行うことができる。

Article 38-7, paragraph (2)

The Medical Information Infrastructure and Medical Fee Examination and Payment Organization or a Federation of National Health Insurance Associations prescribed in Article 45, paragraph (5) of the National Health Insurance Act must, for use in the surveys and analysis under the preceding paragraph, provide the Minister of Health, Labour and Welfare with the information on dispensing of pharmaceuticals, etc. that each of them holds, by the method specified by Order of the Ministry of Health, Labour and Welfare.

医療情報基盤・診療報酬審査支払機構又は国民健康保険法第四十五条第五項に規定する国民健康保険団体連合会は、前項の調査及び分析の用に供するため、厚生労働大臣に対し、それぞれが保有する医薬品調剤等情報を、厚生労働省令で定める方法により提供しなければならない。

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