The Marketing Authorisations for Veterinary Medicinal Products Regulations 1994 No. 3142

Introductory Text
1.Title, commencement and interpretation
2.Circumstances in which these Regulations do not apply
3.Placing veterinary medicinal products on the market
4.Form and manner of application
5.Grant of an authorisation
6.Duties on persons responsible for placing products on the market
7.Products manufactured outside the European Economic Area
8.Duties on an importer who holds a marketing authorisation
9.Variations of authorisations
10.Renewals of authorisations
11.Suspension and revocation
12.Refusal, etc., of a marketing authorisation on grounds relating to safety, quality or efficacy
13.Refusal, etc., of a marketing authorisation on other grounds
14.Confidentiality
15.Fees
16.Offences and penalties
17.Defence
18.Application of the Medicines Act 1968, the Trade Descriptions Act 1968 and the Consumer Protection Act 1987 to marketing authorisations
19.Transitional Provisions
20.Revocations
21.Amendments
Signature
1. SCHEDULE 1
  REQUIREMENTS IN RESPECT OF PRODUCTS OTHER THAN IMMUNOLOGICAL PRODUCTS
2. SCHEDULE 2
  REQUIREMENTS IN RESPECT OF IMMUNOLOGICAL PRODUCTS
  1. 1.The applicant shall comply with the requirements set out in...
  2. 2.(1) Subject to sub-paragraphs (2) and (3) below, the applicant...
3. SCHEDULE 3
  PROCEDURE ON REFERENCE TO APPROPRIATE COMMITTEE OR COMMISSION
4. SCHEDULE 4
  REVOCATIONS
5. SCHEDULE 5
  AMENDMENTS
Explanatory Note