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We assists

the pharmaceutical, biotech industry and CRO´s ...

We encompasses

a broad spectrum of disease areas ...

Local Ethics Committee

available for any clinical research activity at this site ...

Axon Clinical

Clinical Research Center for your clinical research needs

Axon Clinical is dedicated Clinical Research Center for your clinical research needs, providing:

  • GCP-trained clinical staff,
  • experienced coordinators,
  • resources,
  • and infrastructure necessary to conduct human clinical research, helping to answer key scientific and healthcare questions for the benefit of current and future patients.


Few words about our company

assists the pharmaceutical, biotech industry and CRO´s to bring new drugs and devices to the market faster, test new healthcare interventions, drugs and therapies to the highest scientific standards.

We offer our partners in the pharmaceutical industry specialized services and data of highest quality within a broad range of therapeutic areas to meet with today’s requirements for the conductions of clinical trials from Phase I to Phase IV.

We cover a wide range of potential new medicines and also updated versions of currently used medicines, advanced medicinal products and medical devices.

We can carry out your early phase and proof-of-concept studies in both adults and children.

encompasses a broad spectrum of disease areas including:

  • ophtalmology (incl. wAMD, DME, GA)
  • metabolic diseases (incl. Crohn disease, ulcerative colitis, gastroesophageal reflux (GERD), diabetes mellitus (DM)
  • internal medicine (incl. cardiovascular diseases - heart and renal failure, hypertension, diabetes mellitus)
  • neurology (incl. Alzheimer´s Disease, Parkinson´s Disease, Multiple sclerosis, Pain, migraine chronic and acute, headache, lumbosacral radiculopathy)
  • orthopedics (incl. radicular syndrome, tendinopathy, algesiology)
  • ear-nose-and-throat.
  • psychiatric disease
  • dermatology

Local Ethics Committee available for any clinical research activity at this site.

conducts clinical research activities in compliance with:

  • ICH/GCP guidelines,
  • the Clinical Trial Directive,
  • Declaration of Helsinki,
  • local regulations and guidelines
  • as well as the clinical trial specific requirements.

Our efficient initiation process gives a competitive advantage in the race to complete clinical trials on time and within budget. Out team experts in operational efficiency and regulatory compliance could assisst you before and during submission process to Regulatory Agency (SUKL) and Ethics Committees to faster approval timelines and time to market.

Clinical Research Center (address for study shipments):

  • 150 00 Prague 5, Ostrovského 3, Czech Republic 

Local Ethics Committee

Info, members and dates

The Ethics Committee is constituted to ensure the competent review and evaluation of all ethical aspects of the research projects

List of members of the ethics committee.

First name and surname Occupation Employee of EC
appointing authority
Role in EC
MUDr. Martin Wallisch Physician Yes Chairman
Ing. MUDr. Vladimír Strasmajer Physician Yes Vicechairman
RNDr. Richard Vejsada, CSc. Biologist No Member
MUDr. Michaela Homerová Physician No Member
RNDr. Alice Sulamanidze CRM No Member
Ivana Salvetová Study Coord. Yes Member
MUDr. Dana Mrskońćová Physician No Member
MUDr. Hynek Lachmann Physician Yes Member
MUDr. Jan Ernest Physician Yes Member
Jitka Mitisková Secretary Yes Secretary of EC, Lay Member
Jana Preiningerová Physician No Member

Meeting Dates

At least every other month (January, March, May, July, September, November) and upon request as needed.
Upcoming meeting: 30 June 2022 + 25 Aug 2022



Axon Clinical - Etická komise (local IEC) and Company Headquarter (contracts)

Ševce Matouše 26
140 00 Praha 4
Czech Republic

Axon Clinical - Research Center (study shipments + documents for site and EC also)

Ostrovského 3
150 00 Praha 5
Czech Republic


MUDr. Martin Wallisch
Phone: +420 737268655


Ing. MUDr. Vladimír Strasmajer
Phone: +420 737268695

EC secretary:

Jitka Mitisková
Phone: +420 739632800
Fax: +420 241405825

Ethics committee hereby declares that it was established and operates in accordance with its Rules of Procedure in compliance with ICH GCP and valid legal regulations.

Calculation of reimbursement of EC costs

Opinion on local scope
Clinical trial initial submission: 15000 CZK
Opinion of each additional clinical trial site: 5000 CZK
Opinion of the amended documents (required approval): 5000 CZK
Opinion of the notified documents: free of charge
21% VAT shall always be added to the price listed above (except for studies with a billing address outside the Czech Republic)


Project Management team serves as the main point of contact for Sponsor/CRO, and is responsible for the overall trial management and administration.

Managing Director, development, strategy and finance

Vladimír Strasmajer MUDr., Ing.

Managing Director, marketing and quality management

Martin Wallisch MUDr.

GDPR - Data Protection

General Data Protection Regulation: Regulation on the protection of natural persons with regard to the processing of personal data and on the free movement of such data, and repealing Directive 95/46/EC (Data Protection Directive)