Updated to 16 September 2022 (Act No. 30 of 2022 and S.I. No. 460 of 2022)

Contents

Commencement

SectionCommencement DateCommencement Information
Ss. 1-3 1 January 1996 Irish Medicines Board Act 1995 (Commencement) Order 1995 (S.I. No. 345 of 1995), art. 2
Ss. 4(1)(a), 4(1)(b) 19 February 1996 Irish Medicines Board Act 1995 (Commencement) Order 1996 (S.I. No. 40 of 1996), art. 2
Ss. 4(1)(c), 4(1)(d) 1 January 1996 Irish Medicines Board Act 1995 (Commencement) Order 1995 (S.I. No. 345 of 1995), art. 2
S. 4(1)(e) 19 February 1996 Irish Medicines Board Act 1995 (Commencement) Order 1996 (S.I. No. 40 of 1996), art. 2
Ss. 4(1)(f)-4(1)(n), 4(2)-4(5) 1 January 1996 Irish Medicines Board Act 1995 (Commencement) Order 1995 (S.I. No. 345 of 1995), art. 2
Ss. 5-34 1 January 1996 Irish Medicines Board Act 1995 (Commencement) Order 1995 (S.I. No. 345 of 1995), art. 2
S. 35 19 February 1996 Irish Medicines Board Act 1995 (Commencement) Order 1996 (S.I. No. 40 of 1996), art. 2
Ss. 36-38 1 January 1996 Irish Medicines Board Act 1995 (Commencement) Order 1995 (S.I. No. 345 of 1995), art. 2
Sch. 19 February 1996 Irish Medicines Board Act 1995 (Commencement) Order 1996 (S.I. No. 40 of 1996), art. 2

Amendments and other effects

How AffectedAffecting Provision
Application extended S.I. No. 169 of 2000, reg. 3
Saver 15/2013, ss. 1(2), 10(5)(b)
  S.I. No. 538 of 2007, regs. 2, 14
  S.I. No. 551 of 2006, regs. 2, 23(2)
Transfer of certain functions under S.I. No. 418 of 2011, arts. 1(2), 3, schedule 1
  42/2004, ss. 3(1), 4, 58, 59(1), 59(2), 59(3), schedule 3
S. 1(1) constr. refs. "registered medical practitioner"/ "General Register of Medical Practitioners" 25/2007, ss. 1(3), 108(1), 108(2)
S. 1(1) amended 3/2006, ss. 1(7), 10(a)-10(f)
S. 3(4) inserted 14/2013, ss. 1(3), 36
S. 3 fee prescribed S.I No. 599 of 2015, regs. 3, 4, schedule
S. 4(1) amended 3/2006, ss. 1(7), 11(a)(i)
S. 4(1)(b) amended S.I. No. 542 of 2007, regs. 2, 3
S. 4(1)(b) substituted 3/2006, ss. 1(7), 11(a)(ii)
S. 4(1)(c) substituted 3/2006, ss. 1(7), 11(a)(ii)
S. 4(1)(d) substituted 3/2006, ss. 1(7), 11(a)(ii)
S. 4(1)(k) substituted 3/2006, ss. 1(7), 11(a)(iii)
S. 4(1)(o) inserted S.I. No. 304 of 2001, reg. 3(1)
S. 4(1)(p) amended 3/2006, ss. 1(7), 11(a)(iv)
S. 4(1)(p) inserted S.I. No. 444 of 2001, regs. 2(1), 3
S. 4(1)(q) inserted 3/2006, ss. 1(7), 11(a)(v)
S. 4(1)(r) inserted 3/2006, ss. 1(7),11(a)(v)
S. 4(1)(s) inserted 3/2006, ss. 1(7), 11(a)(v)
S. 4(1)(t) inserted 3/2006, ss. 1(7), 11(a)(v)
S. 4(1)(u) inserted 3/2006, ss. 1(7), 11(a)(v)
S. 4(1)(v) substituted S.I. No. 547 of 2017, reg. 4
S. 4(1)(v) inserted 3/2006, ss. 1(7), 11(a)(v)
S. 4(1)(w) inserted S.I. No. 547 of 2017, reg. 4
S. 4(1)(x) inserted S.I. No. 547 of 2017, reg. 4
S. 4(4) substituted 3/2006, ss. 1(7), 11(b)
S. 4(5) substituted 3/2006, ss. 1(7), 11(b)
S. 5(1)(a) amended 3/2006, ss. 1(7), 12
S. 6(5) deleted 1/2017, s. 3
S. 7(9) substituted 3/2006, ss. 1(7), 13
S. 7A inserted 1/2017, s. 4
S. 8(7) deleted 1/2017, s. 5
S. 9(1)(c) inserted S.I. No. 576 of 2002, reg. 3
S. 9(8) substituted 3/2006, ss. 1(7), 14(a)
S. 9(9) substituted 3/2006, ss. 1(7), 14(a)
S. 9(10) inserted 3/2006, ss. 1(7), 14(b)
S. 13 fees prescribed S.I. No. 208 of 2018, reg. 3, schedule
  S.I. No. 557 of 2017, regs. 3, 4, schedule
  S.I. No. 602 of 2016, regs. 3, 4, schedule
  S.I. No. 607 of 2014, regs. 3, 4, schedule
  S.I. No. 501 of 2013, reg. 3, 4, schedule
  S.I. No. 572 of 2012, regs. 3, 4, schedule
  S.I. No. 684 of 2011, reg. 3, schedule
  S.I. No. 632 of 2010, reg. 3, schedule
  S.I. No. 551 of 2009, regs. 2, 5, schedule
  S.I. No. 542 of 2008, regs. 2, 5, schedule
  S.I. No. 866 of 2007, regs. 2, 5, schedule
  S.I. No. 617 of 2006, regs. 2, 5, schedule
  S.I. No. 882 of 2005, regs. 2, 5, schedule
  S.I. No. 877 of 2004, regs. 2, 5, schedule
  S.I. No. 731 of 2003, regs. 2, 5, schedule
  S.I. No. 262 of 2002, regs. 2, 5, schedule
  S.I. No. 44 of 1996, regs. 3, 4, 5, schedule
S. 13(1) in conjunction with s. 4(1)(v), power in regs. under to charge fees S.I. No. 440 of 2013, reg. 3(6)
  S.I. No. 543 of 2012, regs. 2, 5(3)
S. 13(1) substituted 3/2006, ss. 1(7), 15(a)
S. 13(2) amended 3/2006, ss. 1(7), 15(b)
S. 13(5) inserted 3/2006, ss. 1(7), 15(c)
S. 13(6) inserted 3/2006, ss. 1(7), 15(c)
S. 17 transfer of certain functions under 10/2011, ss. 1(2), 6, 9, 20, schedule 2 pt. 1
S. 23 saver from disclosure 30/2014, ss. 1(2), 1(3), 41, schedule 3
  13/1997, ss. 1(2), 1(3), 32, schedule 3
S. 30 repealed with conditions 2/1999, s. 197, schedule 6, col. 3
S. 32 requirement for corrective advertising S.I. No. 541 of 2007, regs. 2, 25(2).
S. 32 application extended S.I. No. 169 of 2000, reg. 3
S. 32 enforcement conditions prescribed S.I. No. 142 of 1998, art. 12
  S.I. No. 256 of 1996, regs. 2, 15
S. 32 application criteria for product authorisations prescribed S.I. No. 142 of 1998, arts. 5-7, schedule 1, pt. II
S. 32 certificate of evidence prescribed S.I. No. 142 of 1998, art. 13, schedule 2
S. 32(f) conditions for grant or renewal of certificate of registration prescribed S.I. No. 142 of 1998, art. 8, schedule 3
S. 32(g) conditions for refusal of licence prescribed S.I. No. 142 of 1998, art. 9
S. 32(2) amended 3/2006, ss. 1(7), 16(a)(i)
S. 32(2)(a) amended 3/2006, ss. 1(7), 16(a)(ii)(I), 16(a)(ii)(II)
S. 32(2)(b) amended 3/2006, ss. 1(7), 16(a)(iii)(I), 16(a)(iii)(II)
S. 32(2)(c) amended 3/2006, ss. 1(7), 16(a)(iv)(I), 16(a)(iv)(II), 16(a)(iv)(III)
S. 32(2)(d) amended 3/2006, ss. 1(7), 16(a)(v)(I), 16(a)(v)(II)
S. 32(2)(e) amended 3/2006, ss. 1(7), 16(a)(vi)
S. 32(2)(f) amended 3/2006, ss. 1(7), 16(a)(vi)
S. 32(2)(g) amended 3/2006, ss. 1(7), 16(a)(vi)
S. 32(2)(h) amended 3/2006, ss. 1(7), 16(a)(vii)(I), 16(a)(vii)(II), 16(a)(vii)(III)
S. 32(2)(i) substituted 3/2006, ss. 1(7), 16(a)(viii)
S. 32(2)(j) substituted 3/2006, ss. 1(7), 16(a)(viii)
S. 32(2)(k) substituted 3/2006, ss. 1(7), 16(a)(viii)
S. 32(2)(l) substituted 3/2006, ss. 1(7), 16(a)(viii)
S. 32(2)(m) substituted 3/2006, ss. 1(7),. 16(a)(viii)
S. 32(2)(m)(i) references construed 20/2007, ss. 1(2), 75(2)
S. 32(2)(n) inserted 3/2006, ss. 1(7), 16(a)(viii)
S. 32(2)(o) inserted 3/2006, ss. 1(7), 16(a)(viii)
S. 32(3) substituted 3/2006, ss. 1(7), 16(b)
S. 32(4) substituted 3/2006, ss. 1(7), 16(b)
S. 32(7) inserted 3/2006, ss. 1(7), 16(c)
S. 32(8) inserted 3/2006, ss. 1(7), 16(c)
S. 32(9) inserted 3/2006, ss. 1(7), 16(c)
S. 32(10) inserted 3/2006, ss. 1(7), 16(c)
S. 32(11) inserted 3/2006, ss. 1(7), 16(c)
S. 32(12) inserted 3/2006, ss. 1(7), 16(c)
S. 32(13) inserted 3/2006, ss. 1(7), 16(c)
S. 32(14) inserted 3/2006, ss. 1(7), 16(c)
S. 32A codes of practice without prejudice to S.I. No. 541 of 2007, regs. 2, 26(3)
S. 32A inserted 3/2006, ss. 1(7), 17
S. 32B applied S.I. No. 538 of 2007, regs. 2, 14
S. 32B codes of practice without prejudice to S.I. No. 541 of 2007, regs. 2, 26(3)
S. 32B inserted 3/2006, ss. 1(7), 17
S. 32B(3)(l) substituted 7/2018, ss. 1(3), 182(a)
S. 32B(12) inserted 7/2018, ss. 1(3), 182(b)
S. 32C codes of practice without prejudice to S.I. No. 541 of 2007, regs. 2, 26(3)
S. 32C inserted 3/2006, ss. 1(7), 17
S. 32D codes of practice without prejudice to S.I. No. 541 of 2007, regs. 2, 26(3)
S. 32D inserted 3/2006, ss. 1(7), 17
S. 32E codes of practice without prejudice to S.I. No. 541 of 2007, regs. 2, 26(3)
S. 32E inserted 3/2006, ss. 1(7), 17
S. 32F codes of practice without prejudice to S.I. No. 541 of 2007, regs. 2, 26(3)
S. 32F inserted 3/2006, ss. 1(7), 17
S. 34(4) application extended S. I. No. 169 of 2000, reg. 3
S. 35(1) amended 3/2006, ss. 1(7), 18
Sch. Title amended 3/2006, ss. 1(7), 19
Sch. 2 inserted 3/2006, ss. 1(7), 20

SIs made under the Act

SectionSIs made under the Act
S. 2 Irish Medicines Board Act 1995 (Establishment) Order 1995 (S.I. No. 346 of 1995)
S. 4(4) Irish Medicines Board (Competent Authority) Order, 1998. (S.I. No. 143 of 1998)
S. 13 Health Products Regulatory Authority (Fees) Regulations 2021 (S.I. No. 744 of 2021)
  Health Products Regulatory Authority (Fees) Regulations 2020 (S.I. No. 654 of 2020)
  Health Products Regulatory Authority (Fees) Regulations 2019 (S.I. No. 700 of 2019)
  Health Products Regulatory Authority (Fees) (No. 2) Regulations 2018 (S.I. No. 531 of 2018)
  Health Products Regulatory Authority (Fees) Regulations 2018 (S.I. No. 208 of 2018)
  Health Products Regulatory Authority (Fees) Regulations 2017 (S.I. No. 557 of 2017)
  Health Products Regulatory Authority (Fees) Regulations 2016 (S.I. No. 602 of 2016)
  Health Products Regulatory Authority (Fees) Regulations 2015 (S.I. No. 599 of 2015)
  Health Products Regulatory Authority (Fees) Regulations 2014 (S.I. No. 607 of 2014)
  Irish Medicines Board (Fees) (Amendment) Regulations 2013 (S.I. No. 165 of 2013)
  Irish Medicines Board (Fees) Regulations 2013 (S.I. No. 501 of 2013)
  Irish Medicines Board (Fees) Regulations 2012 (S.I. No. 572 of 2012)
  Irish Medicines Board (Fees) Regulations 2011 (S.I. No. 684 of 2011)
  Irish Medicines Board (Fees) Regulations 2010 (S.I. No. 632 of 2010)
  Irish Medicines Board (Fees) Regulations 2009 (S.I. No. 551 of 2009)
  Irish Medicines Board (Fees) Regulations 2008 (S.I. No. 542 of 2008)
  Irish Medicines Board (Fees) Regulations 2007 (S.I. No. 866 of 2007)
  Irish Medicines Board (Fees) Regulations 2006 (S.I. No. 617 of 2006)
  Irish Medicines Board (Fees) Regulations 2005 (S.I. No. 882 of 2005)
  Irish Medicines Board (Fees) Regulations 2004 (S.I. No. 877 of 2004)
  Irish Medicines Board (Fees) Regulations 2003 (S.I. No. 731 of 2003)
  Irish Medicines Board (Fees) (Medicinal Products for Human Use) Regulations 2002 (S.I. No. 262 of 2002)
  Irish Medicines Board (Fees) (Amendment) Regulations 2000 (S.I. No. 233 of 2000)
  Irish Medicines Board (Fees) Regulations, 1996 (S.I. No. 44 of 1996)
S. 16 Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 14) Regulations 2021 (S.I. No. 692 of 2021)
S. 32 Medicinal Products (Control of Placing on the Market) (Amendment) Regulations 2022 (S.I. No. 416 of 2022)
  Medicinal Products (Control of Wholesale Distribution) (Amendment) Regulations 2022 (S.I. No. 415 of 2022)
  Medicinal Products (Control of Manufacture) (Amendment) (No. 2) Regulations 2022 (S.I. No. 414 of 2022)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 4) Regulations 2022 (S.I. No. 402 of 2022)
  In Vitro Diagnostic Medical Devices (Registration) Regulations 2022 (S.I. No. 365 of 2022)
  Medicinal Products (Safety Features on Packaging) Regulations 2022 (S.I. No. 270 of 2022)
  In Vitro Diagnostic Medical Devices Regulations 2022 (S.I. No. 256 of 2022)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 3) Regulations 2022 (S.I. No. 84 of 2022)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 2) Regulations 2022 (S.I. No. 57 of 2022)
  Medicinal Products (Control of Manufacture) (Amendment) Regulations 2022 (S.I. No. 43 of 2022)
  Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2022 (S.I. No. 32 of 2022)
  Health Products Regulatory Authority (Fees) Regulations 2021 (S.I. No. 744 of 2021)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 15) Regulations 2021 (S.I. No. 718 of 2021)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 14) Regulations 2021 (S.I. No. 692 of 2021)
  Medical Devices (Registration) Regulations 2021 (S.I. No. 691 of 2021)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 13) Regulations 2021 (S.I. No. 605 of 2021)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 12) Regulations 2021 (S.I. No. 578 of 2021)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 11) Regulations 2021 (S.I. No. 558 of 2021)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 10) Regulations 2021 (S.I. No. 511 of 2021)
  Medical Devices (Amendment) Regulations 2021 (S.I. No. 510 of 2021)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 9) Regulations 2021 (S.I. No. 492 of 2021)
  Medicinal Products (Prescription and Control of Supply) (Amendment) No. 8 Regulations 2021 (S.I. No. 411 of 2021)
  Medical Devices Regulations 2021 (S.I. No. 261 of 2021)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 7) Regulations 2021 (S.I. No. 245 of 2021)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 6) Regulations 2021 (S.I. No. 155 of 2021)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 5) Regulations 2021. (S.I. No. 130 of 2021)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 4) Regulations 2021 (S.I. No. 81 of 2021)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 3) Regulations 2021 (S.I. No. 43 of 2021)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 2) Regulations 2021 (S.I. No. 8 of 2021)
  Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2021 (S.I. No. 2 of 2021)
  Medicinal Products (Control of Wholesale Distribution) (Amendment) Regulations 2021 (S.I. No. 1 of 2021)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 7) Regulations 2020 (S.I. No. 698 of 2020)
  Health Products Regulatory Authority (Fees) Regulations 2020 (S.I. No. 654 of 2020)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 6) Regulations 2020 (S.I. No. 614 of 2020)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 5) Regulations 2020 (S.I. No. 401 of 2020)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 4) Regulations 2020 (S.I. No. 241 of 2020)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 3) Regulations 2020 (S.I. No. 204 of 2020)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 2) Regulations 2020 (S.I. No. 177 of 2020)
  Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2020 (S.I. No. 98 of 2020)
  Health Products Regulatory Authority (Fees) Regulations 2019 (S.I. No. 700 of 2019)
  Medicinal Products (Control Of Manufacture) (Amendment) Regulations 2019 (S.I. No. 219 of 2019)
  Medicinal Products (Control Of Placing On The Market) (Amendment) Regulations 2019 (S.I. No. 218 of 2019)
  Medicinal Products (Control Of Wholesale Distribution) (Amendment) Regulations 2019 (S.I. No. 217 of 2019)
  Medicinal Products (Safety Features On Packaging) Regulations 2019 (S.I. No. 36 of 2019)
  Health Products Regulatory Authority (Fees) (No. 2) Regulations 2018 (S.I. No. 531 of 2018)
  Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2018 (S.I. No. 530 of 2018)
  Medicinal Products (Control of Placing on the Market) (Amendment) Regulations 2018 (S.I. No. 529 of 2018)
  Health Products Regulatory Authority (Fees) Regulations 2018 (S.I. No. 208 of 2018)
  Health Products Regulatory Authority (Fees) Regulations 2017 (S.I. No. 557 of 2017)
  Health Products Regulatory Authority (Fees) Regulations 2016 (S.I. No. 602 of 2016)
  Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2015 (S.I. No. 87 of 2015)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 2) Regulations 2015 (S.I. No. 449 of 2015)
  Health Products Regulatory Authority (Fees) Regulations 2015 (S.I. No. 599 of 2015)
  Medicinal Products (Control of Placing on the Market) (Amendment) Regulations 2014 (S.I. No. 151 of 2014)
  Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2014 (S.I. No. 300 of 2014)
  Medicinal Products (Prescription and Control of Supply) (Amendment) (No. 2) Regulations 2014 (S.I. No. 504 of 2014)
  Health Products Regulatory Authority (Fees) Regulations 2014 (S.I. No. 607 of 2014)
  Medicinal Products (Control of Placing on the Market) (Amendment) Regulations 2013 (S.I. No. 162 of 2013)
  Medicinal Products (Control of Manufacture) (Amendment) Regulations 2013 (S.I. No. 163 of 2013)
  Medicinal Products (Control of Wholesale Distribution) (Amendment) Regulations 2013 (S.I. No. 164 of 2013)
  Irish Medicines Board (Fees) (Amendment) Regulations 2013 (S.I. No. 165 of 2013)
  Irish Medicines Board (Fees) Regulations 2013 (S.I. No. 501 of 2013)
  European Communities (In Vitro Diagnostic Medical Devices) (Amendment) Regulations 2012 (S.I. No. 207 of 2012)
  Medicinal Products (Control of Placing on the Market) (Amendment) Regulations 2012 (S.I. No. 272 of 2012)
  Medicinal Products (Control of Manufacture) (Amendment) Regulations 2012 (S.I. No. 273 of 2012)
  Irish Medicines Board (Fees) Regulations 2012 (S.I. No. 572 of 2012)
  Medicinal Products (Control of Wholesale Distribution) (Amendment) Regulations 2012 (S.I. No. 274 of 2012)
  Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2011 (S.I. No. 525 of 2011)
  Irish Medicines Board (Fees) Regulations 2011 (S.I. No. 684 of 2011)
  Medicinal Products (Control of Placing on the Market) (Amendment) Regulations 2011 (S.I. No. 722 of 2011)
  Medicinal Products (Control of Wholesale Distribution) Regulations 2007 (Amendment) Regulations 2010 (S.I. No. 286 of 2010)
  Medicinal Products (Control of Placing on the Market) Regulations 2007 (Amendment) Regulations 2010 (S.I. No. 287 of 2010
  Medicinal Products (Control of Manufacture) Regulations 2007 (Amendment) Regulations 2010 (S.I. No. 288 of 2010
  Irish Medicines Board (Fees) Regulations 2010 (S.I. No. 632 of 2010)
  Medicinal Products (Control of Wholesale Distribution) Regulations 2007 (Amendment) Regulations 2009 (S.I. No. 2 of 2009)
  Medicinal Products (Control of Placing on the Market) Regulations 2007 (Amendment) Regulations 2009 (S.I. No. 3 of 2009)
  Medicinal Products (Control of Manufacture) Regulations 2007 (Amendment) Regulations 2009 (S.I. No. 4 of 2009)
  Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2009 (S.I. No. 442 of 2009)
  Irish Medicines Board (Fees) Regulations 2009 (S.I. No. 551 of 2009)
  Medicinal Products (Control of Placing on the Market) Regulations 2007 (Amendment) (No. 2) Regulations 2009 (S.I. No. 553 of 2009)
  Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2008 (S.I. No. 512 of 2008)
  Irish Medicines Board (Fees) Regulations 2008 (S.I. No. 542 of 2008)
  Medicinal Products (Revocation of the Medical Preparations (Control of Amphetamine) Regulations 1969) Regulations 2007 (S.I. No. 99 of 2007)
  Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2007 (S.I. No. 201 of 2007)
  Medicinal Products (Control of Wholesale Distribution) Regulations 2007 (S.I. No. 538 of 2007)
  Medicinal Products (Control of Manufacture) Regulations 2007 (S.I. No. 539 of 2007)
  Medicinal Products (Control of Placing on the Market) Regulations 2007 (S.I. No. 540 of 2007)
  Medicinal Products (Control of Advertising) Regulations 2007 (S.I. No. 541 of 2007)
  Irish Medicines Board (Fees) Regulations 2007 (S.I. No. 866 of 2007)
  Irish Medicines Board (Fees) Regulations 2006 (S.I. No. 617 of 2006)
  Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2005 (S.I. No. 510 of 2005)
  Irish Medicines Board (Fees) Regulations 2005 (S.I. No. 882 of 2005)
  Medicinal Products (Amendment) Regulations 2004 (S.I. No. 663 of 2004)
  Irish Medicines Board (Fees) Regulations 2004 (S.I. No. 877 of 2004)
  Medicinal Products (Prescription and Control of Supply) (S.I. No. 877 of 2004)
  Medicinal Products (Prescription and Control of Supply) Regulations 2003 (S.I. No. 540 of 2003)
  Irish Medicines Board (Fees) Regulations 2003 (S.I. No. 731 of 2003)
  Irish Medicines Board (Fees) (Medicinal Products for Human Use) Regulations 2002 (S.I. No. 262 of 2002)
  Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2002 (S.I. No. 627 of 2002)
  Medicinal Products (Control of Paracetamol) Regulations 2001 (S.I. No. 150 of 2001)
  Medicinal Products (Licensing and Sale) (Amendment) Regulations 2001 (S.I. No. 512 of 2001)
  Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 2000 (S.I. No. 116 of 2000)
  Medical Preparations (Labelling and Package Leaflets) (Amendment) Regulations 1999 (S.I. No. 187 of 1999)
  Medicinal Products (Amendment) Regulations 1999 (S.I. No. 188 of 1999)
  Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations 1999 (S.I. No. 271 of 1999)
  Medicinal Products (Licensing and Sale) Regulations, 1998 (S.I. No. 142 of 1998)
  Medicinal Products (Prescription and Control of Supply) (Amendment) Regulations, 1996 (S.I. No. 309 of 1996)
  Medical Preparations (Advertising) (Amendment) Regulations, 1996. (S.I. No. 308 of 1996)
  Medicinal Products (Prescription and Control of Supply) Regulations, 1996 (S.I. No. 256 of 1996)
  Medical Preparations (Licensing and Sale) Regulations, 1996 (S.I. No. 43 of 1996)
  Medical Preparations (Licensing of Manufacture) (Amendment) Regulations, 1996 (S.I. No. 42 of 1996)
  Medical Preparations (Wholesale Licences) (Amendment) Regulations, 1996 (S.I. No. 41 of 1996)
S. 34 Medicinal Products (Amendment) Regulations 1999 (S.I. No. 188 of 1999)