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:

00420 224 910 672

(from 09.00-17.30 CET)

00420 723 694 460

(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:

00420 224 910 672

(09.00-17.30 CET)

00420 723 694 460

(non-stop 24/7)

Pro záležitosti, které se netýkaji farmakovigilance, kontaktujte prosím recepci:

+420 22 491 0000 nebo naše další pobočky.

Pre-clinical and Clinical

Pre-clinical and Clinical Strategy

  • Due diligence of pre-clinical and clinical study data
  • Preparation of strategy reports and plans
  • Scientific advice meetings

Pre-clinical and Clinical Studies

ELC works with a network of validated pre-clinical and clinical research organisations.

Our added value:

  • Independent study document review
  • Oversight and project management at each stage of development
45+
pre-clinical and non-clinical projects

Scope of GCP Audits

Investigator Site

BE/Clinical Study CRO

Third party service provider