Legislation 

Irish Medicines Board Act 1995
Irish Medicines Board (Miscellaneous Provisions) Act 2006

Control of Clinical Trials Act 1987
Control of Clinical Trials and Drugs Act 1990
European Communities (Clinical Trials on Medicinal Products for Human Use) Regulations 2004 (SI 190/2004)
European Communities (Clinical Trials on Medicinal Products for Human Use) (Amendment) Regulations 2004 (SI 878/2004)
European Communities (Clinical Trials on Medicinal Products for Human Use) (Amendment No. 2) Regulations 2006 (SI 374/2006) 
Medicinal Products (Control of Manufacture) Regulations 2007 (SI 539/2007)
European Communities (Control of Placing on the Market) Regulations 2007 (SI 540/2007)
European Communities (Clinical Trials on Medicinal Products for Human Use) (Amendment) Regulations 2009 (SI 1/2009)
European Union (Clinical Trials on Medicinal Products for Human Use) Regulations 2022 (SI 40/2022)
European Union (Clinical Trials on Medicinal Products for Human Use) (National Research Ethics Committees) Regulations 2022 (SI 41/2022)
European Union (Clinical Trials on Medicinal Products for Human Use) (Principal Regulations) 2022 (SI 99/2022) 
European Communities (Clinical Trials on Medicinal Products for Human Use) (Amendment) Regulations 2022 (SI 417/2022)
European Union (Clinical Trials on Medicinal Products for Human Use) (Principal) (Amendment) Regulations 2022 (SI 418/2022) 
European Union (Clinical Trials on Medicinal Products for Human Use) (Amendment) Regulations 2024 (SI 3/2024)

Medicinal Products (Control of Manufacture) Regulations 2007 (SI 539/2007)
Medicinal Products (Control of Manufacture) Regulations 2007 (Amendment) Regulations 2009 (SI 4/2009)
Medicinal Products (Control of Manufacture) Regulations 2007 (Amendment) Regulations 2010 (SI 288/2010)
Medicinal Products (Control of Manufacture) (Amendment) Regulations 2012 (SI 273/2012)
Medicinal Products (Control of Manufacture) (Amendment) Regulations 2013 (SI 163/2013) 
Medicinal Products (Safety Features on Packaging) Regulations 2019 (SI 36/2019)
Medicinal Products (Control of Manufacture) (Amendment) Regulations 2019 (SI 219/2019)
Medicinal Products (Control of Manufacture) (Amendment) Regulations 2022 (SI 43/2022)
Medicinal Products (Safety Features on Packaging) Regulations 2022 (SI 270/2022)
Medicinal Products (Control of Manufacture) (Amendment) (No 2) Regulations 2022 (SI 414/2022)

Medicinal Products (Prescription and Control of Supply) Regulations 2003 (SI 540/2003)
Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2005 (SI 510/2005)
Irish Medicines Board (Miscellaneous Provisions) Act 2006
Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2007 (SI 201/2007)
Medicinal Products (Control of Placing on the Market) Regulations 2007 (SI 540/2007)
Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2008 (SI 512/2008)
Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2009 (SI 442/2009)
Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2011 (SI 525/2011)

Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2014 (SI 300/2014)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.2) Regulations 2014 (SI 504/2014)
Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2015 (SI 87/2015)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 2) Regulations 2015 (SI 449/2015)
Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2018 (SI 530/2018)
Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2020 (SI 98/2020)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.2) Regulations 2020 (SI 177/2020)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.3) Regulations 2020 (SI 204/2020)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.4) Regulations 2020 (SI 241/2020)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.5) Regulations 2020 (SI 401/2020)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.6) Regulations 2020 (SI 614/2020)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.7) Regulations 2020 (SI 698/2020)
Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2021 (SI 2/2021)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 2) Regulations 2021 (SI 8/2021) 
Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 3) Regulations 2021 (SI 43/2021)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.4) Regulations 2021 (SI 81/2021)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 5) Regulations 2021 (SI 130/2021)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 6) Regulations 2021 (SI 155/2021)

Medicinal Products (Prescription and Control of Supply) (Amendment) (No.7)  Regulations 2021 (SI 245/2021)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.8)  Regulations 2021 (SI 411/2021)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.9)  Regulations 2021 (SI 492/2021)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.10)  Regulations 2021 (SI 511/2021)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.11)  Regulations 2021 (SI 558/2021)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.12)  Regulations 2021 (SI 578/2021)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.13)  Regulations 2021 (SI 605/2021)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.14)  Regulations 2021 (SI 692/2021)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.15)  Regulations 2021 (SI 718/2021)
Medicinal Products (Prescription and Control of Supply) Regulations 2022 (SI 32/2022)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.2)  Regulations 2022 (SI 57/2022)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No.3)  Regulations 2022 (SI 84/2022)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 4) Regulations 2022 (SI 402/2022)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No 5) Regulations 2022 (SI 467/2022)
Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2023 (SI 11/2023)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 2) Regulations 2023 (SI 105/2023)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 3) Regulations 2023 (SI 238/2023)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 4) Regulations 2023 (SI 284/2023)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No 5) Regulations 2023 (SI 422/2023)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No 6) Regulations 2023 (SI 451/2023)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No 7) Regulations 2023 (SI 584/2023)
Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2024 (SI 72/2024)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No 2) Regulations 2024 (SI 73/2024)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No 3) Regulations 2024 (SI 162/2024)
Medicinal Products (Prescription and Control of Supply) (Amendment) (No 4) Regulations 2024 (SI 458/2024)

Medicinal Products (Control of Placing on the Market) Regulations 2007 (SI 540/2007)
Medicinal Products (Control of Placing on the Market) Regulations 2007 (Amendment) Regulations 2009 (SI 3/2009)
Medicinal Products (Control of Placing on the Market) Regulations 2007 (Amendment) (No. 2) Regulations 2009 (SI 553/2009)
Medicinal Products (Control of Placing on the Market) Regulations 2007 (Amendment) Regulations 2010 (SI 287/2010) 
Medicinal Products (Control of Placing on the Market) (Amendment) Regulations 2011 (SI 722/2011)
Medicinal Products (Control of Placing on the Market) (Amendment) Regulations 2012 (SI 272/2012)
Medicinal Products (Control of Placing on the Market) (Amendment) Regulations 2013 (SI 162/2013)
Medicinal Products (Control of Placing on the Market) (Amendment) Regulations 2014 (SI 151/2014)
Medicinal Products (Control of Placing on the Market) (Amendment) Regulations 2018 (SI 529/2018)
Medicinal Products (Safety Features on Packaging) (Amendment) Regulations 2019 (SI 36/2019)
Medicinal Products (Control of Placing on the Market) (Amendment) Regulations 2019 (SI 218/2019)
Medicinal Products (Safety Features on Packaging) Regulations 2022 (SI 270/2022)
Medicinal Products (Control of Placing on the Market) (Amendment) Regulations 2022 (SI 416/2022)

Medicinal Products (Control of Wholesale Distribution) Regulations 2007 (SI 538/2007)
Medicinal Products (Control of Wholesale Distribution) Regulations 2007 (Amendment) Regulations 2009 (SI 2/2009)
Medicinal Products (Control of Wholesale Distribution) Regulations 2007 (Amendment) Regulations 2010 (SI 286/2010)
Medicinal Products (Control of Wholesale Distribution) (Amendment) Regulations 2012 (SI 274/2012)
Medicinal Products (Control of Wholesale Distribution) (Amendment) Regulations 2013 (SI 164/2013) 
Medicinal Products (Safety Features on Packaging) Regulations 2019 (SI 36/2019)
Medicinal Products (Control of Wholesale Distribution) (Amendment) Regulations 2019 (SI 217/2019)
Medicinal Products (Control of Wholesale Distribution) (Amendment) Regulations 2021 (SI 1/2021)
Medicinal Products (Safety Features on Packaging) Regulations 2022 (SI 270/2022)
Medicinal Products (Control of Wholesale Distribution) (Amendment) Regulations 2022 (SI 415/2022)

Medicinal Products (Control of Advertising) Regulations 2007 (SI 541/2007)

Health (Pricing and Supply of Medical Goods) Act 2013
Health (Miscellaneous Provisions) Act 2017

Health Products Regulatory Authority (Fees) Regulations 2023 (SI 697/2023)

Veterinary Medicinal Products, Medicated Feed and Fertilisers Regulation Act 2023

European Union (Veterinary Medicinal Products and Medicated Feed) Regulations 2022 (SI 36/2022)

European Union (Protection of Animals used for Scientific Purposes) Regulations 2012 (SI 543/2012)

European Union (Protection of Animals used for Scientific Purposes) (Amendment) Regulations 2013 (SI 434/2013)

European Union (Protection of Animals used for Scientific Purposes) (Amendment) Regulations 2014 (SI 174/2014)

European Union (Protection of Animals used for Scientific Purposes) (Amendment) Regulations 2016 (SI 552/2016) 

European Union (Protection of Animals used for Scientific Purposes) Regulations 2018 (SI 553/2018)

European Union (Protection of Animals used for Scientific Purposes) (Amendment) Regulations 2020 (SI 324/2020)

European Union (Protection of Animals used for Scientific Purposes) (Amendment) Regulations 2022 (SI 205/2022)

S.I. No. 36/2022 - European Union (Veterinary Medicinal Products and Medicated Feed) Regulations 2022  

Veterinary Medicinal Product Regulations 2024 (SI 462/2024)

European Communities (Medical Devices) Regulations 1994 (SI 252/1994)
European Communities (Medical Devices) (Amendment) Regulations 2001 (SI 444/2001)
European Communities (Medical Devices) (Amendment) Regulations 2002 (SI 576/2002)
European Communities (Medical Devices) (Reclassification of Breast Implants) (Amendment) Regulations 2003 (SI 358/2003)
European Communities (Medical Devices) (Tissues of Animal Origin) Regulations 2003 (SI 554/2003)
European Communities (Medical Devices) (Reclassification of Hip, Knee and Shoulder Joint Replacements) (Amendment) Regulations 2007 (SI 92/2007)
European Communities (Medical Devices) (Amendment) Regulations 2009 (SI 110/2009)
European Union (Medical Devices and In Vitro Diagnostic Medical Devices) Regulations 2017 (SI 547/2017)
European Communities (Medical Devices) (Amendment) Regulations 2020 (SI 144/2020) 
European Communities (Medical Devices) (Amendment) (No 2) Regulations 2020 (SI 301/2020)
European Union (National Research Ethics Committee for Clinical Investigations of Medical Devices) Regulations 2021 (SI 260/2021)
Medical Devices Regulations 2021 (SI 261/2021)
Medical Devices (Amendment) Regulations 2021 (SI 510/2021)
Medical Devices (Registration) Regulations 2021 (SI 691/2021)

European Communities (In Vitro Diagnostic Medical Devices) Regulations 2001 (SI 304/2001)
European Communities (Medical Devices) (Amendment) Regulations 2002 (SI 576/2002)
European Communities (In Vitro Diagnostic Medical Devices) (Amendment) Regulations 2012 (SI 207/2012)
European Union (Medical Devices and In Vitro Diagnostic Medical Devices) Regulations 2017 (SI 547/2017) 
European Communities (In Vitro Diagnostic Medical Devices) (Amendment) Regulations 2020 (SI 145/2020)
European Communities (In Vitro Diagnostic Medical Devices) (Amendment) (No 2) Regulations 2020 (SI 302/2020)
In Vitro Diagnostic Medical Devices Regulations 2022 (SI 256/2022)
European Union (National Research Ethics Committees For Performance Studies of In Vitro Diagnostic Medical Devices) Regulations 2022 (SI 257/2022)
In Vitro Diagnostic Medical Devices (Registration) Regulations 2022 (SI 365/2022)
European Union (National Research Ethics Committees For Performance Studies of In Vitro Diagnostic Medical Devices) (Amendment) Regulations 2023 (SI 670/2023)
European Union (National Research Ethics Committees For Performance Studies of In Vitro Diagnostic Medical Devices) Regulations 2023 (SI 671/2023)

European Communities (Active Implantable Medical Devices) Regulations 1994 (SI 253/1994)
European Communities (Medical Devices) (Amendment) Regulations 2001 (SI 444/2001)
European Communities (Active Implantable Medical Devices) (Amendment) Regulations 2009 (SI 109/2009)
European Communities (Active Implantable Medical Devices) (Amendment) Regulations 2020 (SI 300/2020)

European Communities (Quality and Safety of Human Blood and Blood Components) Regulations 2005 (SI 360/2005)
European Communities (Human Blood and Blood Components Traceability Requirements and Notification of Serious Adverse Reactions and Events) Regulations 2006 (SI 547/2006)
European Communities (Quality System for Blood Establishments) Regulations 2006 (SI 562/2006)
European Communities (Quality and Safety of Human Blood and Blood Components) (Amendment) Regulations 2008 (SI 179/2008)
European Communities (Quality and Safety of Human Blood and Blood Components) (Amendment) Regulations 2009 (SI 507/2009)
European Communities (Quality and Safety of Human Blood and Blood Components) (Amendment) Regulations 2011 (SI 329/2011)
European Communities (Quality and Safety of Human Blood Components) (Amendment) Regulations 2015 (SI 494/2015) 
European Communities (Quality System for Blood Establishments) (Amendment) Regulations 2018 (SI 180/2018)

European Communities (Quality and Safety of Human Tissues and Cells) Regulations 2006 (SI 158/2006)
European Communities (Human Tissues and Cells Traceability Requirements, Notification of Serious Adverse Reactions and Events and Certain Technical Requirements) Regulations 2007 (SI 598/2007)
European Communities (Quality and Safety of Human Tissues and Cells) (Amendment) Regulations 2014 (SI 209/2014)
European Communities (Human Tissues and Cells Traceability Requirements, Notification of Serious Adverse Reactions and Events and Certain Technical Requirements) (Amendment) Regulations 2019 (SI 32/2019)
 European Communities (Quality and Safety of Human Tissues and Cells) (Amendment) Regulations 2019 (SI 33/2019)

European Union (Quality and Safety of Human Organs intended for Transplantation) Regulations 2012 (SI 325/2012)
European Union (Quality and Safety of Human Organs Intended for Transplantation) (Amendment) Regulations 2014 (SI 198/2014)

European Union (Cosmetic Products) Regulations 2013 (SI 440/2013)
European Union (Cosmetic Products) (Amendment) Regulations 2015 (SI 512/2015)
European Union (Cosmetic Products) (Amendment) Regulations 2016 (SI 317/2016)
European Union (Cosmetic Products) (Amendment) Regulations 2017 (SI 297/2017)

Misuse of Drugs Act 1977
Misuse of Drugs Act 1984
Misuse of Drugs (Amendment) Act 2015
Misuse of Drugs (Amendment) Act 2016
Misuse of Drugs (Amendment) Act 2016 (Commencement) Order 2017 (SI 172/2017)
Misuse of Drugs Regulations 2017 (SI 173/2017)
Misuse of Drugs (Designation) Order 2017 (SI 174/2017)
Misuse of Drugs (Exemption) Order (SI 175/2017) 
Misuse of Drugs (Amendment) Act 2016 (Commencement) Order 2017 (SI 521/2017)
Misuse of Drugs Act 1977 (Controlled Drugs) (Declaration) Order 2017 (SI 531/2017)
Misuse of Drugs (Amendment) Regulations 2017 (SI 532/2017)
Misuse of Drugs (Designation) (Amendment) Order 2017 (SI 533/2017)
Misuse of Drugs (Prescription and Control of Supply of Cannabis for Medical Use) Regulations 2019 (SI 262/2019)
Misuse of Drugs (Designation) (Amendment) Order 2019 (SI 281/2019)
Misuse of Drugs (Amendment) Regulations 2019 (SI 282/2019)
Misuse of Drugs (Prescription and Control of Supply of Cannabis for Medical Use) (Amendment) Regulations 2019 (SI 583/2019)
Misuse of Drugs (Prescription and Control of Supply of Cannabis for Medical Use) (Amendment) Regulations 2019 (SI 649/2019)
Misuse of Drugs (Amendment) Regulations 2020 (SI 99/2020)
Misuse of Drugs (Prescription and Control of Supply of Cannabis for Medical Use) (Amendment) Regulations 2020 (SI 505/2020)
Misuse of Drugs Act 1977 (Controlled Drugs) (Declaration) Order 2021 (SI82/2021)
Misuse of Drugs (Amendment) Regulations 2021 (SI 121/2021) 
Misuse of Drugs Act 1977 (Controlled Drugs) (Designation) Order 2021 (SI 122/2021)
Misuse of Drugs (Prescription and Control of Supply of Cannabis for Medical Use) (Amendment) Regulations 2021 (SI 557/2021)
Misuse of Drugs Act 1977 (Controlled Drugs) (Declaration) Order (SI 176/2022)
Misuse of Drugs (Amendment) Regulations 2022 (SI 210/2022)
Misuse of Drugs Act 1977 (Controlled Drugs) (Designation) Order 2022 (SI 211/2022)
Misuse of Drugs (Prescription and Control of Supply of Cannabis for Medical Use) (Amendment) Regulations 2022 (SI 237/2022)
Misuse of Drugs (Prescription and Control of Supply of Cannabis for Medical Use) (Amendment) Regulations 2023 (SI 5/2023)
Misuse of Drugs (Amendment) Regulations 2023 (SI 150/2023)
Misuse of Drugs (Amendment) (No.2) Regulations 2023 (SI 156/2023)
Misue of Drugs (Prescription and Control of Supply of Cannabis for Medical Use)  (Amendment) (No. 2) Regulations 2023 (SI 200/2023)

European Communities (Control of Drug Precursors) Regulations 2009 (SI 558/2009)
European Communities (Control of Drug Precursors) (Amendment) Regulations 2022 (SI 555/2022)