Since 2009 SUKL Bulletin is published in electronic form. Full version is available on the czech webpage.
Contents:
- Measures taken in the case of quality defects or adverse reactions to medicinal productsin the month of June 2010
- List of guidelines valid as of July 1, 2010
- Information on amendment of Decree on the marketing authorisation of medicinal products (No 13/2010 Coll.)
- Outline of notifications on the use of non-authorised medicinal products in the month of June 2010
- List of authorised medicinal products where placing on the market of individual batches with the labellingin a foreign language was approved in the month of June 2010
- Information on Czech standards relating to medical devices published in the Bulletin of the COSMT
- Information on documents issued by the European Medicines Agency (EMA)
- Data on applications submitted to SUKL – marketing authorisations and variations thereto
- List of new pharmacies and separate departments for dispensing pharmaceuticals and medical devicesapproved by SUKL in the second quarter of 2010
- List of manufacturers and distributors of pharmaceuticals in the CR approved in the month of June 2010
- List of medicinal products whose marketing authorisation will expire in September 2010
- List of medicinal products with expired marketing authorisation
- List of medicinal products for which maximum price applies in the same amount as proposedby the applicant as of June 30, 2010
- Revocations of marketing authorisations in the period from April 29, 2010 to June 2, 2010
- Authorised medicinal products and variations to marketing authorisations approved in the year 2010
- Medicinal products authorised under the EU centralised procedure and enteredin SUKL database in the year 2010
- List of specific therapeutic programmes approved in the period from June 1, 2010 to June 30, 2010
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