Search Legislation

The Medicines for Human Use (Clinical Trials) (Amendment) (EU Exit) Regulations 2019

 Help about what version

What Version

 Help about advanced features

Advanced Features

 Help about opening options

Opening OptionsExpand opening options

Changes over time for: Section 9

 Help about opening options

Alternative versions:

Changes to legislation:

There are currently no known outstanding effects for the The Medicines for Human Use (Clinical Trials) (Amendment) (EU Exit) Regulations 2019, Section 9. Help about Changes to Legislation

Amendment of regulation 20 (authorisation procedure for clinical trials involving medicinal products with special characteristics)U.K.

This section has no associated Explanatory Memorandum

9.  In regulation 20(1)(a), for paragraph (i) substitute—

(i)which do not have a marketing authorization and are developed by means of one of the following biotechnological processes—

(aa)recombinant DNA technology,

(bb)controlled expression of genes coding for biologically active proteins in prokaryotes and eukaryotes including transformed mammalian cells,

(cc)hybridoma and monoclonal antibody methods, or.

Commencement Information

I1Reg. 9 in force at 31.12.2020 on IP completion day (in accordance with 2020 c. 1, Sch. 5 para. 1(1)), see reg. 1

Back to top

Options/Help