Good Clinical Practice (GCP) - Entry Level
Schedule
Payment by credit card or bank transfer
BOOK & PAY DEADLINE: July 31, 2025
Early bird discount 15% for those who register by 15th of July 2025 No VAT refund. Corporate discounts: 5% for over 3 participants 10% for over 5 participants For more information please contact us at info@avantyo.com or 0726 840 456
COURSE DESCRIPTION
ICH Good Clinical Practice (GCP) training is all about ensuring that clinical trials involving human participants are conducted ethically and to a high standard of quality. The training is based on the ICH E6 (R2) guidelines, which provide an international framework for the design, conduct, recording, and reporting of clinical trials.
The training covers various aspects of clinical trials, including the roles and responsibilities of sponsors, investigators, and other stakeholders, as well as the ethical and regulatory requirements that must be followed. It also provides practical guidance on how to apply GCP principles in real-world research settings.
The main objectives of ICH GCP training include:
- Protecting the rights, safety, and well-being of trial participants: Ensuring that participants are treated ethically and their rights are respected throughout the trial.
- Ensuring the integrity and credibility of clinical trial data: Making sure that the data collected is accurate, reliable, and can be trusted for regulatory and scientific purposes.
- Facilitating mutual acceptance of clinical trial results: Harmonising standards across different regions to support global collaboration in drug development.
- Promoting transparency and accountability: Encouraging the registration of clinical trials and the reporting of results to maintain public trust.
ONLINE INSTRUCTOR-LED COURSE
Organizers: Avantyo Institute of Clinical Research
Location: Online
Duration: 2-day sessions for 4 hours each day
Training days: August 1-2, 2025
Training time: From 2 PM GMT+2
Language: English / Romanian
Trainer: Dr. Catalina Sarbu
Attendance only by online reservation. Booking available after registering on this site.
WHY ATTEND OUR GCP ENTRY LEVEL COURSE?
Comprehensive Curriculum: Our course covers all aspects of GCP, including regulatory requirements, ethical considerations, and practical implementation.
Expert Trainers: Learn from experienced professionals like Catalina Sarbu, who bring real-world insights and expertise to the training.
Interactive Learning: Engage in interactive sessions, case studies, and discussions to enhance your understanding and application of GCP principles.
Flexible Learning Options: Attend the course online via Zoom, making it accessible to professionals worldwide.
Certification: Upon completion, receive an internationally recognised certification from TransCelerate, demonstrating your competence in GCP. Participants will be able to download their Participation Certificates directly from their accounts on www.avantyo.com
Discount: Participants in Module 1 – GCP Training for Entry Level will enjoy a 15% discount on Module 2 – GCP Training for Advanced Level. This offer provides an excellent opportunity for those eager to continue their professional development in the field of clinical research.
For discounts and assistance, or if you wish to be placed on a waiting list for the next course, or require any additional information, please contact us at diana.lupu@avantyo.com (+40 0726 840 456). Be sure to mention your specific educational requirements in clinical trials.
This training offers the opportunity to acquire basic Good Clinical Practice (GCP) knowledge for professionals willing to enter the clinical trials field. It is designed for a wide range of participants, including:
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Investigators and Clinical Study Teams: Individuals involved in the planning, conduct, and oversight of clinical trials.
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Clinical Referrals: Such as clinicians, general practitioners (GPs), and other healthcare providers who refer patients for clinical trials.
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Study Coordinators and Study Nurses: Professionals responsible for the day-to-day management of clinical trials, ensuring adherence to protocols and regulatory requirements.
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Physicians and Pharmacists: Medical professionals who play a crucial role in the administration and monitoring of clinical trials, ensuring patient safety and data integrity.
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Life Science Graduates: Individuals with a background in life sciences who are looking to transition into the clinical research field.
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Clinical Trials Assistants (CTAs): Professionals who provide administrative support to clinical research teams, helping to ensure the smooth conduct of trials.
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Clinical Research Coordinators (CRCs): Key personnel who manage the logistics and documentation of clinical trials, playing a vital role in the coordination between the clinical site and the research sponsor.
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Other Medical-Related Professionals: Including those in allied health fields, who aspire to build a career in the clinical research scientific domain.
This comprehensive training program aims to equip participants with the foundational knowledge of GCP principles, enhancing their ability to contribute effectively to the clinical trials process. It fosters the development of essential skills needed to navigate the complexities of clinical research, from ethical considerations to regulatory compliance and data management.
By participating in this training, professionals will be better prepared to embark on a rewarding career in clinical research, playing a crucial role in the advancement of medical science and patient care.
Dr. Catalina SARBU Secretary General of the Romanian Association of CROs (ACCSCR) Romania
- 2022-2025 Secretary General of the Romanian Association of CROs (ACCSCR) Romania
- 2000-2022 Director of the Romanian Representative office of PAREXEL Nederland BV
- Former President of the CRO Association in Romania (ACCSCR)
- General Practitioner – Center of Hematology, Ploiesti, Romania
- Saint Antoine University, Paris, France - Hematology and Blood Transfusion, 1-year courses
- University of Medicine and Pharmacy, Bucharest, Romania - Medical Doctor Degree
"Everything you learn is a benefit to your role or your future roles, and the Entry Level GCP course from Avantyo thought us the most important aspects regarding the Clinical Trial World. The training was interactive, with many explanations and exercises. In addition, the trainer was experienced in this field, kind, well prepared and ready to answer all our questions."
"The GCP training was interactive and with a lot of good information, well good explained, with a lot of examples which help you to make connections. The trainer was very nice, ready to help us with all the information that we need and all the explanations to help us to understand everything."
For previous events, please access one of the following links.
