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Innovation in education

We pride ourselves on providing the most up-to-date content for our students to learn each course.

Conferencing
Training
Consulting

Get better every day with our trainings and courses!

Perfectly tailored training modules for all medical staff

Clinical Research Associate (CRA) Training Program – Entry & Advanced Level
Clinical Research Associate (CRA) Training Program – Entry & Advanced Level The CRA is responsible for ensuring that the clinical trial is conducted in accordance with Good Clinical Practice (GCP) protocol and applicable legislation.
Intensive Study Nurse Training
Intensive Study Nurse Training 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 Good Clinical Practice (GCP) Training Program – Entry & Advanced Level
ICH Good Clinical Practice (GCP) Training Program – Entry & Advanced Level
Clinical Trials for Investigators
Clinical Trials for Investigators This course addresses to physicians, both newly graduates or experienced, interested to contribute to the progress of medical research.
Clinical Trials for Study Coordinators
Clinical Trials for Study Coordinators
Postgraduate course for Project Management in Clinical Trials
Postgraduate course for Project Management in Clinical Trials 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.
Clinical Trials Fundamentals for Life Science Graduates
Clinical Trials Fundamentals for 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.
Pharmacovigilance
Pharmacovigilance
Pioneering Progress: Understanding the Nuances of Innovative Phase 1 Clinical Trial Design
Pioneering Progress: Understanding the Nuances of Innovative Phase 1 Clinical Trial Design
Clinical Data Management
Clinical Data Management Clinical Data Management course that introduces core data processes, regulatory standards, and the full CDM lifecycle. It provides practical experience with EDC systems and data quality activities to prepare learners for real world clinical research.

Experience conferences made simple with us!

“Annual symposium, conferencing, roundtable meetings and workshops held throughout the year.

The Bucharest International Clinical Trials Symposium BICS Symposium

Our flagship event – The Bucharest International Clinical Trials Symposium (BICS) – is held annually and brings together hundreds of senior‑level delegates from academia, industry, and both private and public healthcare sectors, alongside representatives of regulatory authorities from across Europe.

Each edition features distinguished international speakers – leading figures and key opinion leaders within the clinical research community – who deliver a programme of timely, influential and expertly curated presentations. Topics typically encompass clinical operations, regulatory affairs, outsourcing strategies, patient enrolment, and the growing emphasis on patient centricity, offering attendees a comprehensive and forward‑looking perspective on the evolving clinical trials landscape.

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Roundtables and Workshops Roundtables and Workshops

Our Roundtables and Workshops provide refined, high‑value forums for senior specialists across the clinical research landscape to exchange insight, experience and practical solutions. Roundtables offer an intimate environment in which executive‑level participants gather for a focused 3‑ to 4‑hour session, typically over lunch or dinner, to discuss a single, clearly defined topic under the guidance of a seasoned expert in the field.

Complementing this, our Workshops deliver highly interactive half‑day or full‑day programmes designed to inform and update both newcomers and experienced professionals. Bringing together representatives from academia, CROs, pharmaceutical and biotech sponsors, third‑party vendors, patient organisations, medical media, IT and legal sectors, these sessions explore the specificities and evolving demands of clinical trials through structured, practical engagement.

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Conferences Conferences

Our Conferences bring together senior professionals from across the clinical research landscape for focused, high‑level discussions on emerging trends, regulatory developments and operational best practice. These gatherings unite voices from academia, industry, healthcare and regulatory bodies to consider the issues that matter most – transparency, trust, access, innovation and meaningful progress.

Each event is designed to encourage thoughtful exchange – fostering strategic insight, informed debate and effective cross‑sector collaboration. Underpinning these conversations is a shared recognition that clinical research extends far beyond process and protocol; it represents hope, reassurance and the possibility of better outcomes for the individuals and communities it ultimately serves.

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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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