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About SIDC
eKolok
Quality Policy
Leadership of SIDC
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Fees Guide
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Medical Devices
Scope of activities
Instructions
List of registered / announced medical devices, codes and economic operators from 1.1.2018
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Pharmacopoeia
Pharmacopoeia department
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Instructions
Form for submitting clinical trial documents to the SIDC
Labelling requirements for Investigational Medicinal Product
Adverse event/reaction in a clinical trial - Reporting requirements in the Slovak Republic
Main changes in Slovak Drug Law - Clinical trials (human)
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