Medicinal Products (Control of Wholesale Distribution) Regulations, 2007 (Amendment) Regulations, 2009

• Jurisdiction: Ireland

S.I. No. 2 of 2009

MEDICINAL PRODUCTS (CONTROL OF WHOLESALE DISTRIBUTION) REGULATIONS 2007 (AMENDMENT) REGULATIONS 2009

Notice of the making of this Statutory Instrument was published in

“Iris Oifigiúil” of 16th January, 2009.

The Minister for Health and Children, in exercise of the powers conferred on her by section 32 of the Irish Medicines Board Act 1995 (No. 29 of 1995), as amended by section 16 of the Irish Medicines Board (Miscellaneous Provisions) Act 2006 (No. 3 of 2006) and as adapted by the Health (Alteration of Name of Department and Title of Minister) Order 1997 ( S.I. No. 308 of 1997 ), and for the purpose of giving full effect to Directive 2001/83/EC (as amended by Article 28 of Regulation (EC) No. 1394/2007), hereby make the following regulations:-

Citation

1. These Regulations may be cited as the Medicinal Products (Control of Wholesale Distribution) Regulations 2007 (Amendment) Regulations 2009.

2. These Regulations shall be construed as one with the Medicinal Products (Control of Wholesale Distribution) Regulations 2007 ( S.I. No. 538 of 2007 ) and may be cited together with those Regulations as the Medicinal Products (Control of Wholesale Distribution) Regulations 2007 and 2009.

Commencement

3. These Regulations shall come into force on 14 January 2009.

Interpretation

4. (1) In these Regulations:

‘principal regulations’ mean the Medicinal Products (Control of Wholesale Distribution) Regulations 2007 ( S.I. No. 538 of 2007 ).

Amendment of Regulations

5. Regulation 4(1) of the principal regulations is amended—

(a) by inserting the following after the definition of “Act”:

“ ‘advanced therapy medicinal product’ means a product as defined in Article 2 of the advanced therapy regulation;

‘advanced therapy regulation’ means Regulation (EC) No. 1394/2007 of the European Parliament and of the Council of 13 November 2007 on advanced therapy medicinal products 9 ;”

(b) by substituting the following for the definition of “2001 Directive”:

“ ‘2001 Directive’ means Directive 2001/83/EC of the European Parliament and of the Council on the Community code relating to medicinal products for human use 10 as amended by—

(a) Directive 2002/98/EC of the European Parliament and of the Council setting standards of quality and safety for the collection, testing, processing, storage and distribution of human blood and blood components 11 ,

(b) Commission Directive 2003/63/EC amending Directive 2001/83/EC on the...