The Export Control (Amendment) (No. 3) Order 2010

Type Statutory-Instrument
Publication 2010-11-29
State In force
Department Queen's Printer of Acts of Parliament
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Made: 29th November 2010

Laid before Parliament: 29th November 2010

Coming into force: 30th November 2010

The Secretary of State, in exercise of the powers conferred by sections 1, 6 and 7 of the Export Control Act 2002[^f00001], makes the following Order:

Citation, commencement and expiration

1

2

(4A) (1) Subject to articles 17 and 26, no person shall export pharmaceutical goods for human use containing the active ingredient thiopental sodium if paragraph (2) or (3) applies. (2) This paragraph applies where the destination is the United States of America. (3) This paragraph applies where the destination is not the United States of America but the exporter knows that the final destination of the goods is the United States of America.

Signed

Mark Prisk — Minister of State for Business Enterprise — Department for Business, Innovation and Skills — 29th November 2010

Explanatory note

(This note is not part of the Order)

EXPLANATORY NOTE

This Order amends the Export Control Order 2008 (S.I. 2008/3231). Article 2 introduces a new control on the export of pharmaceutical goods for human use containing the active ingredient thiopental sodium to the United States of America and makes other related amendments. This Order will cease to have effect on 28 November 2011.

The Explanatory Memorandum is available alongside the instrument on the OPSI website. The Impact Assessment is currently being prepared.

Footnotes

[^f00001]: 2002 c.28.

[^f00002]: S.I. 2008/3231; relevant amending instruments are S.I. 2009/1852 and S.I. 2010/121.

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