2010 No. 1882
The Medicines for Human Use (Advanced Therapy Medicinal Products and Miscellaneous Amendments) Regulations 2010 (revoked)F1
Made
Laid before Parliament
Coming into force
F1. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Citation, commencement and interpretationF11
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Disapplication of section 7 of the Medicines Act 1968 to exempt advanced therapy medicinal productsF12
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Licence conditions for exempt advanced therapy medicinal productsF13
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
TraceabilityF14
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Traceability in the event of bankruptcy or liquidation of holder of manufacturer's licence for exempt ATMPF15
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Amendment of the Medicines (Standard Provisions for Licences and Certificates) Regulations 1971F16
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Amendment of the Medicines (Applications for Manufacturer's and Wholesale Dealer's Licences) Regulations 1971F17
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Amendment of the Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994F18
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Amendment of the Medicines for Human Use (Clinical Trials) Regulations 2004F19
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Amendment of the Medicines for Human Use (Manufacturing, Wholesale Dealing and Miscellaneous Amendments) Regulations 2005F110
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
F1. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
F1SCHEDULE 1Requirement that holders of manufacturer's licences comply with certain obligations in relation to the manufacture and assembly of exempt advanced therapy medicinal products
F1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
F1SCHEDULE 2Standard provisions for manufacturer's licences insofar as those licences relate to exempt advanced therapy medicinal products
F11
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
F12
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
F1SCHEDULE 3Requirement that holders of wholesale dealer's licences comply with certain obligations in relation to exempt advanced therapy medicinal products
F1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
F1SCHEDULE 4Standard provisions for wholesale dealer's licences insofar as those licences relate to exempt advanced therapy medicinal products
F1
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
F1SCHEDULE 5Amendments to the Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994
Amendment of regulation 1F11
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Amendment of Schedule 1F12
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Amendment of Schedule 3F13
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Amendment of Schedule 6F14
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Regulations revoked (14.8.2012) by The Human Medicines Regulations 2012 (S.I. 2012/1916), reg. 1(2), Sch. 35 (with Sch. 32)