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Statutory Instrument

The Medicines (Products for Human Use) (Fees) (Amendment) Regulations 2025

Citation
S.I. 2025/317
As at
Sections
31
Section 1Citation, commencement and extent

(1) These Regulations may be cited as the Medicines (Products for Human Use) (Fees) (Amendment) Regulations 2025.

(2) These Regulations come into force on 1st April 2025.

(3) These Regulations extend to England and Wales, Scotland and Northern Ireland.

Section 2Amendment of the Medicines (Products for Human Use) (Fees) Regulations 2016

The Medicines (Products for Human Use) (Fees) Regulations 2016 are amended in accordance with regulations 3 to 31.

Section 3New regulation 3A

After regulation 3 (interpretation of Part 2), insert—

Fee for scientific or other advice

(3A)

(1) Unless regulation 5 applies, the fee specified in paragraph (2) is payable by a person with whom the licensing authority holds a meeting in order to provide scientific or other advice relating to a medicinal product.

(2) The fee payable by a person in relation to a meeting referred to in paragraph (1) is—

(a) £17,516, if the advice provided at that meeting is on a matter of high complexity;

(b) £13,137, if the advice provided at that meeting is on a matter of medium complexity;

(c) £8,758, if the advice provided at that meeting is on a matter of low complexity;

(d) £986, if the advice provided at that meeting is on a matter of simple complexity.

(3) In paragraph (2), a matter is of—

(a) high complexity if it requires more than twelve assessor days;

(b) medium complexity if it requires more than seven, but not more than twelve, assessor days;

(c) low complexity if it requires more than three, but not more than seven, assessor days;

(d) simple complexity if it requires not more than three assessor days.

(4) If the person paying the fee in accordance with paragraph (1) consents, the licensing authority may provide any advice in writing instead of at a meeting.

(5) In this regulation—

“ assessor day ” means—

in the case of an assessor who is a member of the senior civil service, one assessor working for one day;

in the case of an assessor who is not a member of the senior civil service, one assessor working for two days.

“ medicinal product ”, in paragraph (e) of the definition of scientific or other advice in this regulation, includes a substance incorporated in a device which, if used separately, may be considered to be a medicinal product as defined in Article 1(2) of the 2001 Directive;

“ scientific or other advice ” includes—

scientific advice on an application for an EU marketing authorisation, or an application for the variation of an EU marketing authorisation, in relation to a medicinal product;

advice before the publication of advertising of a medicinal product by the holder of a marketing authorisation for that product on whether that advertising conforms to the requirements of the Human Medicines Regulations;

pharmacovigilance advice;

regulatory advice;

advice in relation to—

scientific or regulatory issues relating to the development of a medicinal product or a type of medicinal product;

the design of pharmaceutical or pre-clinical tests, or clinical trials, for a medicinal product or a type of medicinal product;

the management of risk in relation to a medicinal product or a type of medicinal product which is under development, or is being marketed;

other scientific or regulatory issues relating to a medicinal product or a type of medicinal product after an EU marketing authorisation has been granted for that product or a product of that type.

Section 4Omission of regulation 4

Omit regulation 4 (fee for scientific advice: application for, or variation to, EU marketing authorisation) .

Section 5Amendment of regulation 5

In regulation 5(1) (fee for scientific advice: classification of a medicinal product) —

(a) in sub-paragraph (a), for “£3,039” substitute “£8,758” ;

(b) in sub-paragraph (b), for “£3,986” substitute “£8,758” .

Section 6Omission of regulation 6

Omit regulation 6 (fee for advertising advice) .

Section 7Omission of regulation 7

Omit regulation 7 (fee for pharmacovigilance advice) .

Section 8Amendment of regulation 8

In regulation 8 (fee for advice on labelling or leaflets) , for “£2,421” substitute “£3,757” .

Section 9Omission of regulation 9

Omit regulation 9 (fee for regulatory advice) .

Section 10Omission of regulation 10

Omit regulation 10 (fee for advice for other purposes) .

Section 11Amendment of regulation 10A

In regulation 10A(1) (waiver for advice given to small and medium companies) , for “4 to 10” substitute “3A to 8” .

Section 12Amendment of regulation 11

In regulation 11 (time for payment of fees under regulations 4 to 10), for “4 to 10” , in each place it occurs (including the heading to the regulation), substitute “3A to 8” .

Section 13Amendment of regulation 14

In regulation 14 (fee for applications for additional copy certificates) , for “£75” substitute “£82” .

Section 14Amendment of regulation 15

In regulation 15 (fees for applications for certificates and copy certificates by exporters of medicinal products) —

(a) in paragraph (1)(a), for “£167” substitute “£182” ;

(b) in paragraph (1)(b), for “£75” substitute “£82” .

Section 15Amendment of regulation 19A

In regulation 19A (fees for certification of plasma master files) —

(a) in paragraph (1), for “£9,140” substitute “£11,126” ;

(b) in paragraph (2)(a), for “£344” substitute “£419” ;

(c) in paragraph (2)(b), for “£1,308” substitute “£1,593” .

Section 16Amendment of regulation 19B

In regulation 19B (fee for certification of vaccine antigen master files) , for “£9,140” substitute “£11,126” .

Section 17Amendment of regulation 19C

In regulation 19C (fees for assessment of post-authorisation safety studies) for “£9,140” , in both places it occurs, substitute “£9,949” .

Section 18Amendment of regulation 19E

In regulation 19E(2) (fee for assessment of periodic safety update reports) —

(a) in sub-paragraph (a), for “£979” substitute “£1,066” ;

(b) in sub-paragraph (b), for “£490” substitute “£534” .

Section 19Amendment of regulation 19EA

In regulation 19EA (fee for assessment of clinical trial annual safety reports) , for “£248” substitute “£343” .

Section 20Amendment of regulation 21

In regulation 21(1) (fees for notification of changes and reports for broker’s registrations) , for “£283” substitute “£345” .

Section 21Amendment of regulation 22

In regulation 22(1) (fees for notification of changes and compliance reports for active substance registrations) , for “£283” substitute “£309” .

Section 22Amendment of regulation 27

In regulation 27(1) (fees for renewals of certain manufacturer’s licences) , for “£196” substitute “£214” .

Section 23Amendment of regulation 41

In regulation 41 (fees for applications for membership and certificates) —

(a) in paragraph (1), for “£129” substitute “£141” ;

(b) in paragraph (2), for “£68” substitute “£75” .

Section 24Amendment of regulation 42

In regulation 42(1) (fee for a review upon oral representations or a person appointed hearing) , for “£11,000” substitute “£11,974” .

Section 25Amendment of regulation 44

In regulation 44(1) (interpretation), in the definition of “standard variation”—

(a) in sub-paragraph (o), at the end, omit “or” ;

(b) in sub-paragraph (p), for “authorisation.” substitute “authorisation; or” ;

(c) after sub-paragraph (p), insert—

(q) a change to any packaging of the product, including the container or other form of packaging immediately in contact with the medicinal product, any packaging into which the container or other form of packaging immediately in contact with the product is placed, or to a leaflet that accompanies the product and contains information for the user of the product.

Section 26Amendment of regulation 47

In regulation 47 (fees for variations of certificates)—

(a) in paragraph (1)(a)—

(i) in paragraph (i), for “£123” substitute “£149” ;

(ii) in paragraph (ii), for “£62” substitute “£75” ;

(b) in paragraph (1)(b), for “£123” substitute “£149” ;

(c) in paragraph (2)(a)—

(i) in paragraph (i), for “£243” substitute “£296” ;

(ii) in paragraph (ii), for “£243” substitute “£296” ;

(iii) in paragraph (iii), for “£123” substitute “£149” ;

(iv) in paragraph (iv), for “£62” substitute “£75” ;

(d) in paragraph (2)(b), for “£243” substitute “£296” .

Section 27Amendment of Schedule 2

(1) Schedule 2 (capital fees for applications for, and variations to, marketing authorisations, licences, registrations and certificates) is amended as follows.

(2) In paragraph 21 (standard variation application for a homoeopathic medicinal product)—

(a) in sub-paragraph (o), at the end, omit “or” ;

(b) in sub-paragraph (p), for “Directive.” substitute “Directive; or” ;

(c) after sub-paragraph (p), insert—

(q) a change to any packaging of the product, including the container or other form of packaging immediately in contact with the medicinal product, any packaging into which the container or other form of packaging immediately in contact with the product is placed, or to a leaflet that accompanies the product and contains information for the user of the product.

(3) In paragraph 24(5) (marketing authorisations) , in the table (fees for marketing authorisation applications)—

(a) in item 1 (major application)—

(i) in entry (a), for “£32,705” substitute “£39,811” ;

(ii) in entries (b) to (d), for “£68,663”, in each place it occurs, substitute “£83,580” ;

(iii) in entry (e), for “£20,281” substitute “£24,688” ;

(iv) omit entry (f);

(v) omit entry (g);

(vi) in entry (h), for “£102,028” substitute “£124,194” ;

(b) in item 2 (complex application)—

(i) in entries (a) to (c), for “£19,063”, in each place it occurs, substitute “£23,205” ;

(ii) in entry (d), for “£11,487” substitute “£13,983” ;

(iii) omit entry (e);

(iv) omit entry (f);

(v) in entry (g), for “£28,207” substitute “£34,335” ;

(c) in item 3 (standard application)—

(i) in entries (a) to (c), for “£6,985”, in each place it occurs, substitute “£8,503” ;

(ii) in entry (d), for “£6,361” substitute “£7,743” ;

(iii) omit entry (e);

(iv) omit entry (f);

(v) in entry (g), for “£10,342” substitute “£12,589” ;

(d) in item 4 (simple application)—

(i) in entries (a) to (c), for “£2,820”, in each place it occurs, substitute “£3,433” ;

(ii) omit entry (d);

(iii) omit entry (e);

(iv) in entry (f), for “£2,820” substitute “£3,433” ;

(e) in item 5 (parallel import licence applications)—

(i) in entry (a), for “£1,971” substitute “£2,400” ;

(ii) in entry (b), for “£8,722” substitute “£10,617” ;

(iii) in entry (c), for “£19,998” substitute “£24,343” ;

(f) in item 6 (change of ownership application), for “£486” substitute “£592” .

(4) In paragraph 25(1) (fees where application includes reclassification) —

(a) in sub-paragraph (a), for “£33,003” substitute “£40,173” ;

(b) in sub-paragraph (b), for “£8,978” substitute “£10,929” .

(5) In paragraph 28(4)(b) (application for multiple authorisations) , for “£1,308” substitute “£1,593” .

(6) In paragraph 28A (application by pre-assessment of modules) —

(a) in sub-paragraphs (1)(a) to (c), for “£25,507”, in each place it occurs, substitute “£31,049” ;

(b) in sub-paragraphs (2)(a) to (c), for “£4,766”, in each place it occurs, substitute “£5,802” .

(7) In paragraph 29 (authorisation for a national homoeopathic product)—

(a) in sub-paragraph (4), in the table (fees for homoeopathic marketing authorisation applications)—

(i) in the second column (fee for applications in respect of products prepared from not more than 5 homoeopathic stocks)—

(aa) in entry 1, for “£517” substitute “£630” ;

(bb) in entry 2, for “£808” substitute “£984” ;

(cc) in entry 3, for “£1,088” substitute “£1,325” ;

(ii) in the third column (fee for other applications)—

(aa) in entry 1, for “£732” substitute “£892” ;

(bb) in entry 2, for “£1,014” substitute “£1,235” ;

(cc) in entry 3, for “£1,312” substitute “£1,598” ;

(b) in sub-paragraph (6), for “£2,154” substitute “£2,622” ;

(c) in sub-paragraph (7), for “£7,185” substitute “£8,746” ;

(d) in sub-paragraph (8), for “£635” substitute “£773” .

(8) In paragraph 30(1) (manufacturer’s licences and authorisations) —

(a) in sub-paragraph (a), for “£201” substitute “£245” ;

(b) in sub-paragraph (b), for “£378” substitute “£461” ;

(c) in sub-paragraph (c), for “£3,457” substitute “£4,209” .

(9) In paragraph 31 (wholesale dealer’s licences) —

(a) in sub-paragraph (1), for “£1,983” substitute “£2,159” ;

(b) in sub-paragraph (5), for “£439” substitute “£478” .

(10) In paragraph 33(1) (active substance registrations) —

(a) in paragraph (a), for “£3,457” substitute “£3,763” ;

(b) in paragraph (b), for “£1,983” substitute “£2,159” .

(11) In paragraph 34 (clinical trial authorisations) —

(a) in sub-paragraph (a), for “£3,366” substitute “£4,656” ;

(b) in sub-paragraph (b), for “£248” substitute “£343” .

(12) In paragraph 35 (traditional herbal registrations) —

(a) in sub-paragraph (1), in the second column (fee payable) of the table (fee for application for traditional herbal registration)—

(i) in entry 1 (complex registration application)—

(aa) in entry (a), for “£4,846” substitute “£5,899” ;

(bb) in entry (b), for “£7,269” substitute “£8,848” ;

(ii) in entry 2 (standard registration application)—

(aa) in entry (a), for “£2,423” substitute “£2,950” ;

(bb) in entry (b), for “£3,634” substitute “£4,424” ;

(iii) in entry 3 (reduced registration application category II)—

(aa) in entry (a), for “£807” substitute “£983” ;

(bb) in entry (b), for “£1,212” substitute “£1,476” ;

(iv) in entry 4 (reduced registration application category I)—

(aa) in entry (a), for “£539” substitute “£657” ;

(bb) in entry (b), for “£807” substitute “£983” ;

(v) in entry 5 (change of ownership application), for “£486” substitute “£592” .

(b) in sub-paragraph (3)—

(i) in paragraph (a), for “£1,077” substitute “£1,311” ;

(ii) in paragraph (b), for “£2,154” substitute “£2,622” ;

(c) in sub-paragraph (4), for “£7,186” substitute “£8,748” ;

(d) in sub-paragraph (5), for “£638” substitute “£777” ;

(e) in sub-paragraph (6), for “£2,154” substitute “£2,622” .

(13) In paragraph 35A (early access to medicines scheme fees), in the second column (fee payable) of the table (fees for early access to medicines scheme applications) —

(a) in entry 1, for “£3,986” substitute “£4,852” ;

(b) in entry 2, for “£25,643” substitute “£31,214” ;

(c) in entry 3, for “£12,821” substitute “£15,607” ;

(d) in entry 4, for “£8,309” substitute “£10,115” ;

(e) in entry 5, for “£4,154” substitute “£5,057” .

(14) In paragraph 38(6) (marketing authorisations)—

(a) in the second column (column 2 fee payable) of Table 1 (fees for applications for variations of marketing authorisations falling within the scope of Chapter II of Commission Regulation (EC) No 1234/2008 ) —

(i) in item 1 (application for a single kind variation)—

(aa) in entries (a) and (b), for “£344”, in both places it occurs, substitute “£419” ;

(bb) in entry (c), for “£2,742” substitute “£3,338” ;

(cc) in entry (d), for “£8,462” substitute “£10,301” ;

(ii) in item 2 (applications for a group)—

(aa) in entry (a), for “£344” substitute “£419” ;

(bb) in entry (b), for “£1,255” substitute “£1,528” ;

(cc) in entry (c), for “£2,973” substitute “£3,619” ;

(dd) in entry (d), for “£8,671” substitute “£10,555” ;

(b) in the second column (fee payable) of Table 2 (fees for applications for variations of marketing authorisations falling within the scope of Chapter IIa of Commission Regulation (EC) No 1234/2008 and of marketing authorisations in force in Great Britain) —

(i) in item 1, for “£344” substitute “£419” ;

(ii) in item 2, for “£1,308” substitute “£1,593” ;

(iii) in item 3, for “£9,140” substitute “£11,126” ;

(iv) in item 4, for “£33,003” substitute “£40,173” ;

(v) in item 5, for “£684” substitute “£833” ;

(vi) in item 6, for “£1,817” substitute “£2,212” ;

(vii) in item 7, for “£9,911” substitute “£12,065” ;

(viii) in item 8, for “£28,904” substitute “£35,184” ;

(c) in the second column (fee payable) of Table 3 (fees for reclassification variation applications) —

(i) in entry (a), for “£33,003” substitute “£40,173” ;

(ii) in entry (b), for “£8,978” substitute “£10,929” .

(15) In paragraph 40(1) (reclassification of marketing authorisations) , for “£1,308” substitute “£1,593” .

(16) In paragraph 41 (variation of marketing authorisation: national homoeopathic products)—

(a) in sub-paragraph (a), for “£243” substitute “£296” ;

(b) in sub-paragraph (b), for “£374” substitute “£456” ;

(c) in sub-paragraph (c), for “£123” substitute “£149” .

(17) In paragraph 42(1) (variation of parallel import licence) —

(a) in paragraph (a), for “£33,003” substitute “£40,173” ;

(b) in paragraph (b), for “£8,978” substitute “£10,929” ;

(c) in paragraph (c), for “£393” substitute “£479” .

(18) In paragraph 43 (manufacturer’s authorisations and licences) —

(a) in sub-paragraph (a), for “£283” substitute “£345” ;

(b) in sub-paragraph (b), for “£565” substitute “£688” .

(19) In paragraph 44 (variation of manufacturer’s authorisations and licences) , for “£283” substitute “£345” .

(20) In paragraph 45 (wholesale dealer’s licences) , for “£535” substitute “£652” .

(21) In paragraph 46 (variation of wholesale dealer’s licence) , for “£283” substitute “£345” .

(22) In paragraph 47 (variation of a broker’s registration) , for “£283” substitute “£345” .

(23) In paragraph 48 (variation of an active substance registration) , for “£283” substitute “£309” .

(24) In paragraph 49(1) (clinical trial authorisations) , for “£248” substitute “£302” .

(25) In paragraph 50 (traditional herbal registrations)—

(a) in sub-paragraph (a), for “£240” substitute “£293” ;

(b) in sub-paragraph (b), for “£635” substitute “£773” ;

(c) in sub-paragraph (c), for “£7,186” substitute “£8,748” ;

(d) in sub-paragraph (d), for “£152” substitute “£186” .

(26) In paragraph 54 (a set of changes) —

(a) in sub-paragraph (1)—

(i) in paragraph (a), for “£570” substitute “£992” ;

(ii) in paragraph (b), for “£361” substitute “£440” ;

(b) in sub-paragraph (2), for “£205” substitute “£224” .

(27) In paragraph 56 (renewal of a marketing authorisation) —

(a) in sub-paragraphs (a) and (b), for “£822”, in both places it occurs, substitute “£1,239” ;

(b) in sub-paragraph (c), for “£10,650” substitute “£16,042” .

(28) In paragraph 57(2) (renewal of multiple marketing authorisations) —

(a) in paragraphs (a)(i) and (a)(ii), for “£822”, in both places it occurs, substitute “£1,239” ;

(b) in paragraph (b)(i), for “£10,650” substitute “£16,042” .

(29) In paragraph 57A (capital fee for conducting a major safety review) —

(a) in sub-paragraph (a), for “£56,415” substitute “£61,408” ;

(b) in sub-paragraph (b), for “£65,555” substitute “£71,357” ;

(c) in sub-paragraph (c), for “£74,694” substitute “£81,305” ;

(d) in sub-paragraph (d), for “£83,834” substitute “£91,254” .

(30) For paragraph 57B (capital fee for testing of samples by the appropriate authority) substitute—

(57B)

(1) The fee payable under regulation 19F(1) in connection with the submission of a sample of a batch of a medicinal product is £5,093 for each day taken to examine the sample for testing, the appropriate documentation (as defined in regulation 60A of the Human Medicines Regulations) or both (as the case may be), and the fee payable is to be adjusted pro rata for each period taken of less than 1 day.

(2) In this paragraph, a “ day ” means a period of 8 hours and 30 minutes.

Section 28Amendment of Schedule 3

(1) Schedule 3 (fees for inspections) is amended as follows.

(2) In paragraph 2(1) (fees: general) —

(a) in paragraph (1)(a), for “£3,651” substitute “£5,251” ;

(b) in paragraph (1)(b), for “£1,825” substitute “£2,625” .

(3) In paragraph 5 (wholesale dealer’s licence: general) —

(a) in sub-paragraphs (a) and (b), for “£2,662” , in both places it occurs, substitute “£4,136” ;

(b) in sub-paragraph (b), for “£1,331” substitute “£2,068” .

(4) In paragraph 6(2) (wholesale dealer’s licence: traditional herbal medicinal products) —

(a) in paragraph (a), for “£1,023” substitute “£1,114” ;

(b) in paragraphs (b) and (c), for “£1,880” , in both places it occurs, substitute “£2,047” .

(5) In paragraph 7(3) (wholesale dealer’s licences: inspection of short duration) , for “£1,331” substitute “£2,068” .

(6) In paragraph 8 (broker’s registrations) —

(a) in sub-paragraph (1)—

(i) in paragraphs (a) and (b), for “£2,662” , in both places it occurs, substitute “£3,241” ;

(ii) in paragraph (b), for “£1,331” substitute “£1,621” ;

(b) in sub-paragraph (3), for “£640” substitute “£780” .

(7) In paragraph 9 (active substance registrations) —

(a) in sub-paragraph (1)(a)—

(i) in sub-paragraphs (i) and (ii), for “£3,651” , in both places it occurs, substitute “£3,975” ;

(ii) in sub-paragraph (ii), for “£1,825” substitute “£1,988” ;

(b) in sub-paragraph (1)(b)—

(i) in sub-paragraphs (i) and (ii), for “£2,662” , in both places it occurs, substitute “£2,898” ;

(ii) in sub-paragraph (ii), for “£1,331” substitute “£1,449” ;

(c) in sub-paragraph (3)—

(i) in paragraph (a), for “£871” substitute “£949” ;

(ii) in paragraph (b), for “£640” substitute “£697” .

(8) In paragraph 10 (office-based inspections) —

(a) in sub-paragraph (a), for “£2,562” substitute “£4,924” ;

(b) in sub-paragraph (b), for “£1,862” substitute “£3,810” .

Section 29Amendment of Schedule 4

(1) Schedule 4 (Periodic fees for licences) is amended as follows.

(2) In paragraph 5 (marketing authorisations) , in column 2 (fee payable) of the table (periodic fees for holding a marketing authorisation)—

(a) in entry 1, for “£10,681” substitute “£11,627” ;

(b) in entry 2, for “£338” substitute “£368” ;

(c) in entry 3(a), for “£10,681” substitute “£11,627” ;

(d) in entry 3(b)(i), for “£2,671” substitute “£2,908” ;

(e) in entry 3(b)(ii), for “£1,332” substitute “£1,450” ;

(f) in entries 3(b)(iii), (c) and (d), for “£338”, in each place it occurs, substitute “£368” ;

(g) in entries 3(e) to (h), for “£84”, in each place it occurs, substitute “£92” .

(3) In paragraph 6 (marketing authorisation: where Part 2 of the Act applies) , for “£338” substitute “£368” .

(4) In paragraph 7 (marketing authorisation: derivatives) —

(a) in sub-paragraph (a), for “£10,681” substitute “£11,627” ;

(b) in sub-paragraph (b), for “£7,209” substitute “£7,847” .

(5) In paragraph 11(1) and (2) (manufacturer’s licences or manufacturing authorisations) , for “£515”, in both places it occurs, substitute “£561” .

(6) In paragraph 12 (wholesale dealer’s licences) —

(a) in sub-paragraph (1), for “£317” substitute “£346” ;

(b) in sub-paragraph (2), for “£189” substitute “£206” .

(7) In paragraph 15(1)(b) (additional amount for manufacturer’s licences and wholesale dealer’s licences which relate to special medicinal products)—

(a) for Table 1 (additional periodic fee in connection with notices for imported special medicinal products) substitute—

Additional periodic fee in connection with notices for imported special medicinal products

(b) in the second column (additional amount) of Table 2 (Additional periodic fee in connection with the number of different special medicinal products notified for import)—

(i) in the entry “1 to 5”, for “£100” substitute “£122” ;

(ii) in the entry “6 to 10”, for “200” substitute “£244” ;

(iii) in the entry “11 to 20”, for “£400” substitute “£487” ;

(iv) in the entry “21 to 50”, for “£1,000” substitute “£1,218” ;

(v) in the entry “51 to 100, for “£2,000” substitute “£2,435” ;

(vi) in the entry “101 to 200”, for “£4,000” substitute “£,4,869” ;

(vii) in the entry “For each additional 100 special medicinal products notified for import above 200”, for “£2,000” substitute “£4,869 plus £2,435 for each additional 100 special medicinal products notified for import” .

(8) In paragraph 16 (traditional herbal registrations) , for “£84” substitute “£92” .

Section 30Amendment of Schedule 5

(1) Schedule 5 (fees for certificates of registration) is amended as follows.

(2) In the table—

(a) in the second column (fees for applications in respect of products prepared from not more than 5 homoeopathic stocks)—

(i) in item 1, for “£159” substitute “£194” ;

(ii) in item 2, for “£478” substitute “£582” ;

(iii) in item 3, for “£501” substitute “£610” ;

(iv) in item 5, for “£430” substitute “£524” ;

(v) in item 7, for “£790” substitute “£962” ;

(b) in the third column (fees for other applications)—

(i) in item 1, for “£393” substitute “£479” ;

(ii) in item 2, for “£704” substitute “£857” ;

(iii) in item 3, for “£638” substitute “£777” ;

(iv) in item 5, for “£563” substitute “£686” ;

(v) in item 7 for “£1,034” substitute “£1,259” .

Section 31Amendment of Schedule 7

(1) Schedule 7 (waiver, reduction or refund of capital fees) is amended as follows.

(2) In paragraph 11(1) (scientific advice: paediatric indications), for “regulation 4” substitute “regulation 3A” .

31 sections

Cite this legislation

The Medicines (Products for Human Use) (Fees) (Amendment) Regulations 2025 (legislation.gov.uk, OGL v3.0). Retrieved via LawPlayer, https://lawplayer.com/uk/act/uksi-2025-317

Contains public sector information licensed under the Open Government Licence v3.0.

OGL-3

本頁資料來源:legislation.gov.uk (The National Archives)·整理提供:法律人 LawPlayer· lawplayer.com