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Innovation in education

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Conferencing made easy with us!

Annual symposium, roundtable meetings and workshops throughout the year

Clinical Trials Symposium Conferences & Symposium

Our leading event „The Clinical Trials Symposium“ is organized annually and gathers hundreds of senior level delegates from academia, industry, private and public healthcare sectors as well as representatives of regulatory bodies across Europe.

Well-known international speakers, including key opinion leaders in the clinical research field, are attending and presenting hot topics covering clinical operations, regulatory affairs, outsourcing strategies as well as patient enrollment and patient centricity aspects.

Next symposium: 11.10.2019 - Bucharest, Romania
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Roundtables Roundtables

The concept of Roundtables shall offer a platform for specialists at the executive level from the various segments of the clinical research arena to meet and vividly network over a concentrated session of 3 to 4 hours, across lunch or dinner, to informally and openly share their challenges and solutions in the given segment. Only one topic shall be addressed during the Roundtable, under the moderation of one senior expert in the given area.

Last roundtable: 15.05.2020 - Online
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Roundtables Workshops

The Workshops are highly interactive events, taking place over 1/2 day or 1 full day with the aim to educate and update both newcomers as well as experienced personnel representing a large spectrum of players in the clinical research segment – academia, CROs, pharma&biotech Sponsors, 3rd party vendors, patient representatives, medical media, IT, legal experts etc. – with regard to various aspects and the specificities of clinical trials.

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Get better every day!

Perfectly tailored training modules for all medical staff

Clinical Research Associate (CRA) Training Program
Next date: 17-18 September 2020 Clinical Research Associate (CRA) Training Program The CRA is responsible for ensuring that the clinical trial is conducted in accordance with Good Clinical Practice (GCP) protocol and applicable legislation.
Study nurses
Next date: 30th March - 3rd April 2020
Postponed to undetermined date, due to COVID 19
Study nurses The Clinical Research Nurse, under the guidance and supervision of the Principal Investigator (PI), ensures that the clinical trials are conducted in accordance with the study protocol.
ICH GCP Good Clinical Practice (GCP) course is designed to prepare research staff in the conduct of clinical trials with human participants. This year will be available in Bucharest-Romania, Chisinau-Moldavia and Tbilisi-Georgia.
Investigators / Study coordinators
Investigators / Study coordinators This course addresses to physicians, both newly graduates or experienced, interested to contribute to the progress of medical research.
Postgraduates for Project Management
Postgraduates for Project Management The program provides a structured approach to developing knowledge and skills which will enable you to develop your own research portfolio or, more commonly, assist in the management of an existing portfolio.
Life science graduates
Life science graduates An introductory course in the clinical research field enabling you to understand the various components and tasks linked to the delivery of a clinical research project.
GDPR in Clinical Research
GDPR in Clinical Research The aim of this training is to explain in much more depth the legal basis for processing personal data in the context of clinical trials.

Get an expert advice

Personalized consultation from our experts!

Contact our expert team!

Our team members are glad to offer expertise related to start-up, planning and logistics aspects of clinical research projects with a focus on Eastern Europe. We offer tailor-made support related to most efficient approaches when it comes to: regulatory strategies, feasibilities - smart selection of „proven“ clinical sites across various regions & therapeutic areas, selection and organization of clinical lab needs and selection of suitable CRAs/CTAs.

As a first step, we kindly ask you to fill in the contact form and we come back to you in the shortest time.

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We thoroughly evaluate your request!

Following an initial request and follow-up discussions, a mutual CDA (confidentiality agreement) shall be signed. AVANTYO assigns a responsible project manager to evaluate the time and budget needed to design most efficient strategy to fit your needs. Once the tasks and deliverables, as well as the linked budget are agreed, AVANTYO´s experts start project execution.

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We deliver tailor-made solutions!

The solutions are presented to you in writing as well as via e-meetings or F2F. Our goal is to give you access to our proven, most efficient selection of matching and truly reliable partners/vendors based on our long-year expertise, reputation and networking in the clinical research area, leading to fast and high quality execution of your clinical trial(s).

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