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Request for an Advisory Opinion from the EFTA Court by Oslo tingrett dated 16 June 2014 in the case of Pharmaq AS v Intervet International BV (Case E-16/14)
- CELEX number:
- E2014P0016
- Form:
- Judicial information
- Legal basis:
- Author:
- EFTA Court
- Date of document:
- 16/06/2014
- Number of pages:
- 2
Summary of Community decisions on marketing authorisations in respect of medicinal products from 15 November to 15 December 2001 (Decisions taken pursuant to Article 14 of Directive 75/319/EEC or Article 22 of Directive 81/881/EEC)
- CELEX number:
- 52001XC1228(02)
- Form:
- Communication
- Legal basis:
- 31975L0319 - A14
- 31981L0851 - A22
- Author:
- European Commission
- Date of document:
- 28/12/2001; Date of publication
- Number of pages:
- 2
Commission Directive 2000/37/EC of 5 June 2000 amending Chapter VIa 'Pharmacovigilance' of Council Directive 81/851/EEC on the approximation of the laws of the Member States relating to veterinary medicinal products (Text with EEA relevance)
No longer in force
- CELEX number:
- 32000L0037
- Form:
- Directive
- Legal basis:
- 31981L0851 - A42DECIES
- Author:
- European Commission
- Date of document:
- 05/06/2000
- Number of pages:
- 3
Commission Regulation (EC) No 1146/98 of 2 June 1998 amending Regulation (EC) No 541/95 concerning the examination of variations in the terms of a marketing authorisation granted by a competent authority of a Member State
No longer in force
- CELEX number:
- 31998R1146
- Form:
- Regulation
- Legal basis:
- 31975L0319 - A15
- 31981L0851 - A23
- Author:
- European Commission
- Date of document:
- 02/06/1998
- Number of pages:
- 4
Commission Regulation (EC) No 541/95 of 10 March 1995 concerning the examination of variations to the terms of a marketing authorization granted by a competent authority of a Member State
No longer in force
- CELEX number:
- 31995R0541
- Form:
- Regulation
- Legal basis:
- 31975L0319 - A15
- 31981L0851 - A23
- Author:
- European Commission
- Date of document:
- 10/03/1995
- Number of pages:
- 8
Commission Directive 91/412/EEC of 23 July 1991 laying down the principles and guidelines of good manufacturing practice for veterinary medicinal products
In force
- CELEX number:
- 31991L0412
- Form:
- Directive
- Legal basis:
- 31981L0851 - A27BIS
- 31990L0677
- Author:
- European Commission
- Date of document:
- 23/07/1991
- Number of pages:
- 4
Domain: All, Legal basis – CELEX number: 31981L0851, Search language: English