《人类药品条例》第20123条第8条（一般解释）的修改第20条（药品的混合）修改5.第213条的修改（第12部分的解释）第6条第214条的修正（只出售药品或供应处方药）第223条（对医生和牙医的豁免）8.第228条的修正案（对某些卫生专业人员开的处方的豁免）9.第229条的修正案（对国家卫生服务机构和地方当局供应的豁免）10.第248条的修正案（对某些收集和交付的豁免安排）11.对第346条的修订（国务卿对某些规定进行审查）12.对附表17的修订（某些人的销售、供应或管理豁免）13.对附表23（药房记录中的详情）的修订签署解释性说明

Introductory Text1.Citation and commencement2.Amendment of the Human Medicines Regulations 20123.Amendment of regulation 8 (general interpretation)4.Amendment of regulation 20 (mixing of medicines)5.Amendment of regulation 213 (interpretation of Part 12)6.Amendment of regulation 214 (sale or supply of prescription only medicines)7.Amendment of regulation 223 (exemptions for doctors and dentistsetc)8.Amendment of regulation 228 (exemptions relating to prescriptions given by certain health professionals)9.Amendment of regulation 229 (exemption for supply by national health service bodies and local authorities)10.Amendment of regulation 248 (exemption for certain collection and delivery arrangements)11.Amendment of regulation 346 (Secretary of State to carry out a review of certain provisions)12.Amendment of Schedule 17 (exemption for sale, supply or administration by certain persons)13.Amendment of Schedule 23 (particulars in pharmacy records)SignatureExplanatory Note