ePrivacy and GPDR Cookie Consent by TermsFeed Generator
Archive

There is an Archive of all articles sorted by date of publication.

2007    2008    2009    2010    2011    2012    2013    2014    2015    2016    2017    2018    2019    2020    2021    2022    2023    2024   

<<   January February March April May June July August September October November December   >>


Published aricles: 11


List of reimbursed medicinal products valid as of 1.6.2015

Acting in compliance with Section 39n(1) of Act No. 48/1997 Coll., on Public Health Insurance, as amended (“Act”), the State Institute for Drug Control publishes the List of Prices and Reimbursements for Medicinal Products and Foods for Special Medicinal Purposes (“List”).  


SUKL Bulletin 5/2015

SUKL Bulletin 5/2015 was published 27. 5. 2015  


Decree No 62/2015 Coll.

Decree No 62/2015 Coll. implementing certain provisions of the Act on Medical Devices came into effect on the Third of April, 2015.  


Act on Medical Devices

Act No 268/2014 Coll. on Medical Devices came into effect on the First of April, 2015. This Act is a complex legal regulation which covers issue of Medical devices in the Czech Republic.    


Legislation


Launch of the new Registry of Medical Devices

State Institute for Drug Control (SUKL), the Ministry of Health (Ministry of Health) and the Coordination Centre for Departmental Medical Information Systems (KSRZIS) inform the public about the launch of the public Registry of Medical Devices (RZPRO).  


Registration and Notification


EDUROAM – roaming between institutions

State Institute for Drug Control (SÚKL) has been part of the project EDUROAM that allows access to the network in many locations not only in the Czech Republic.   


Launch of the new Registry of Medical Devices

State Institute for Drug Control (SUKL), the Ministry of Health (Ministry of Health) and the Coordination Centre for Departmental Medical Information Systems (KSRZIS) inform the public about the launch of the public Registry of Medical Devices (RZPRO).  


Reporting of serious adverse event (SAE)


Reporting of field safety corrective action