Reporting of adverse events ONLY

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:

+420 224 910 672

(from 09.00-17.30 CET)

+420 226 251 459

(non-stop 24/7)

To contact us about any other issue please call:

+420 22 491 0000or our regional offices.

Hlášení nežádoucích príhod

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:

+420 224 910 672

(09.00-17.30 CET)

+420 226 251 459

(non-stop 24/7)

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

Quality Management System development and implementation to identify gaps in processes which could impact quality and regulatory compliance

Compliance support

Development of Procedures, Work Instructions and Trainings to ensure compliance with current regulations and company policies

Quality check

Perform quality checks of all processes to assess the overall quality, performance and regulatory compliance

Internal audits

Periodic review of processes via internal audits and handling of Deviations and Corrective and Preventive Action (CAPA) management

Third party audits

Perform Business Partners and Vendors’ audits

Inspections support

Support in Authorities’ Inspections and propose and implement Corrective and Preventive Actions