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Next: Clinical Trials Symposium on 18th November, 2022

GCP Advanced Level

This course presents for participants already familiar with basic ICH-GCP(Good Clinical Practice) principles, information over The Clinical Trials Regulation and Inspection Readiness and allow attendees to acquire in depth knowledge over application of GCP through practical exercises.


Organizers: AVANTYO  -Institute of Clinical Research 

Location: Hotel Novotel

Language: English

Trainer: Dr. Ingrid Klingmann - President of European Forum for Good Clinical Practice


Attendance only by online reservation. Booking available after registering on this site.

For discounts and assistance please contact us:

info@avantyo.com

diana.lupu@avantyo.com (0726 840 456)

andrei.grigore@avantyo.com (0728 453 248)

The participants to Module 1 – GCP Training for Entry Level organized by Avantyo, will benefit
of 15% discount to Module 2 – GCP Training for Advanced Level.


Successful attendance of our GCP training as demonstrated in a final multiple-choice test will provide you with the internationally recognized “EFGCP GCP Certificate of Completion”. The course is recognized by TransCelerate Minimum Criteria of GCP Training Courses.


If you would like to be placed on a waiting list for the next course or you need something else, please let us know at info@avantyo.com. Don’t forget to mention your specific education needs in clinical trials.

Privacy Policy & GDPR

The Module 2, GCP Training – Advanced  Level is dedicated to clinical Research Specialists (Clinical Trials Assistant (CTA), Junior Clinical Associates, Clinical Research Associates (CRA), Senior Clinical Research Associates (CRA), investigators, study nurses and other professionals who have already graduated the Entry-Level Module 1 of GCP Training as all other clinical studies specialists (physicians, pharmacists, biologists, biochemists etc.) willing to enhance their clinical trials knowledge.

Dr. Ingrid Klingmann, President of European Forum for Good Clinical Practice (EFGCP), Belgium PHARMAPLEX bv, EFGCP, PharmaTrain Federation

Ingrid Klingmann, MD, PhD, European Forum for Good Clinical Practice (EFGCP), Pharmaplex bv, Brussels, has 30 years of practical experience with planning and performance of clinical trials from a sponsor and investigator perspective in the pharmaceutical industry, CRO and academic institution. Through her activities in multi-stakeholder not-for-profit organisations like EFGCP, she gained broad experience in ethical, quality and regulatory challenges in clinical research and possible approaches to solutions.

  • Physician, specialized in General Medicine, Clinical Pharmacology and Pharmaceutical Medicine with over 30 years of experience in different senior medical, operational and managerial functions in the pharmaceutical industry, CROs and clinical trial sites with focus on clinical trial design and management, ethical and regulatory aspects.
  • Since January 2003 she has her pharmaceutical development and site management support consulting company.
  • Dr Klingmann is Chairman of the Board of the European Forum for Good Clinical Practice (EFGCP). On behalf of EFGCP she was and is involved in different FP7- and IMI-funded projects (ICREL, PatientPartner, PharmaTrain, EUPATI, Combacte-NET, PARADIGM and ConCEPTION) and with her company in the FP7-funded paediatric LENA project. Her broad professional background as a physician with experience in patient care, clinical development, site management and patient engagement enables Dr Klingmann to bridge the gaps between the interests and skills of all different stakeholders in medicines development to develop new patient-relevant treatments more efficiently.
  • Dr Klingmann is also President of PharmaTrain Federation, the not-for-profit organisation focussing on global standardisation and improvement of post-graduate training in medicines development sciences. She also teaches on different clinical research and regulatory affairs topics in diploma and master courses at the University of Bonn, Germany, University of Basel, Switzerland, and the Université Libre de Bruxelles, Belgium.

For previous events, please access one of the following links.

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