Patients should always seek the advice of a doctor or pharmacist in case of adverse events.
If you wish to report an adverse event to ELC Group s.r.o., please find the contact information below:
To contact us about any other issue please call:
Pacienti by meli vždy požádat o radu svého lékare nebo lékárníka v prípade výskytu nežádoucích príhod.
Pokud chcete nahlásit nežádoucí príhodu spolecnosti ELC Group s r.o., prosím využijte kontaktních údaju níže:
Pro záležitosti, které se netýkaji farmakovigilance, kontaktujte prosím recepci:
+420 22 491 0000 nebo naše další pobočky.
Our Quality Management department provides a comprehensive and tailored batch of activities to support your needs.
Quality Management System development and implementation to identify gaps in processes which could impact quality and regulatory compliance
Development of Procedures, Work Instructions and Trainings to ensure compliance with current regulations and company policies
Perform quality checks of all processes to assess the overall quality, performance and regulatory compliance
Periodic review of processes via internal audits and handling of Deviations and Corrective and Preventive Action (CAPA) management
Perform Business Partners and Vendors’ audits
Support in Authorities’ Inspections and propose and implement Corrective and Preventive Actions
