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Authorisation, import and manufacture of veterinary medicines
Summary of EU Legislation
- Form:
- Summaries of EU legislation
- Summarised document(s):
- Date of last review:
- 02/08/2022
Ingredients used in medicines – guidance for importers and distributors
Summary of EU Legislation
- Form:
- Summaries of EU legislation
- Summarised document(s):
- Date of last review:
- 03/12/2015
High safety standards and streamlined procedures for EU clinical trials
Summary of EU Legislation
- Form:
- Summaries of EU legislation
- Summarised document(s):
- Date of last review:
- 30/05/2022
EU rules on the authorisation, import and production of veterinary medicines
Summary of EU Legislation
- Form:
- Summaries of EU legislation
- Summarised document(s):
EU rules for new medical products based on genes and cells
Summary of EU Legislation
- Form:
- Summaries of EU legislation
- Summarised document(s):
- Date of last review:
- 16/10/2015
Safe medicines for Europeans — European Medicines Agency
Summary of EU Legislation
- Form:
- Summaries of EU legislation
- Summarised document(s):
- Date of last review:
- 08/03/2019
Clinical Trials
Summary of EU Legislation
- Form:
- Summaries of EU legislation
- Summarised document(s):
- Date of last review:
- 28/05/2020
Colouring matters for medicinal products
Summary of EU Legislation
- Form:
- Summaries of EU legislation
- Summarised document(s):
- Date of last review:
- 19/05/2022
Supplementary protection certificates for medicines and plant protection products
Summary of EU Legislation
- Form:
- Summaries of EU legislation
- Summarised document(s):
- Date of last review:
- 10/10/2019
European Pharmacopoeia - EUR-Lex
Summary of EU Legislation
- Form:
- Summaries of EU legislation
- Summarised document(s):
- Date of last review:
- 08/04/2014
Subdomain: Summaries of EU legislation, Directory code, 3rd level: Proprietary medicinal products, Search language: Slovenian, Include archived summaries: True