Print Options
PrintThe Whole
Instrument
PrintThe
Schedules
only
Changes over time for: The Genetically Modified Animal Feed (Scotland) Regulations 2004 (Schedules only)
Llinell Amser Newidiadau
This timeline shows the different points in time where a change occurred. The dates will coincide with the earliest date on which the change (e.g an insertion, a repeal or a substitution) that was applied came into force. The first date in the timeline will usually be the earliest date when the provision came into force. In some cases the first date is 01/02/1991 (or for Northern Ireland legislation 01/01/2006). This date is our basedate. No versions before this date are available. For further information see the Editorial Practice Guide and Glossary under Help.
Version Superseded: 22/04/2011
Status:
Point in time view as at 15/11/2010.
Changes to legislation:
There are currently no known outstanding effects for the The Genetically Modified Animal Feed (Scotland) Regulations 2004.
Changes to Legislation
Revised legislation carried on this site may not be fully up to date. At the current time any known changes or effects made by subsequent legislation have been applied to the text of the legislation you are viewing by the editorial team. Please see ‘Frequently Asked Questions’ for details regarding the timescales for which new effects are identified and recorded on this site.
Regulation 2(a)
SCHEDULESSPECIFIED COMMUNITY PROVISIONS
PART I S
Provision of the Community Regulation | Subject Matter |
---|
Article 16.2 | Prohibition on placing on the market feed referred to in Article 15.1 unless it is covered by an authorisation and satisfies relevant conditions of the authorisation. |
PART II S
Provision of the Community Regulation | Subject Matter |
---|
Article 20.6 | Requirement that products in respect of which the Commission have adopted a measure under Article 20.6 shall be withdrawn from the market. |
Article 21 | Requirement that the authorisation holder and the parties concerned must comply with conditions or restrictions imposed on an authorisation for that product, and the authorisation holder must comply with post–market monitoring requirements |
Article 21.3 | Requirement to inform the Commission of any new scientific or technical information relating to a product, which might influence the evaluation of the safety in use of the feed, or any prohibition or restriction on the feed in a third country. |
Article 25 | Requirement for certain labelling indications. |
Yn ôl i’r brig