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Welcome to OnlineGCP’s portfolio page where you could learn more about our multi-language training solutions. We aim to design and provide clinical training, which satisfies both international and local directives, in keeping up with the growth of strictness and importance of ICH-GCP and other clinical regulations internationally. In order to learn more, please visit our dedicated websites where there is detailed information regarding the specifics of the given training and its purchase.

If you are part of an organization in search of clinical training, whose needs are not covered by the portfolio variety, please contact us and tell us more about the solution your organization requires. We will do our best to assist you in coming up with the best solution for your organization.

ICH GCP adapted for the UK in English
The UK version of the GCP online training includes a comprehensive guide to ICH-GCP, as well as UK-specific rules and regulations. It covers all the new changes/amendments proposed in the EU Directive 2005/28/EC and the UK Regulations. The Summary of Proposed Changes to current Regulations is attached for ready reference and those changes are also included in all relevant chapters of the course. The certificate provided is endorsed by the Faculty of Pharmaceutical Medicine of the Royal College of Physicians of the United Kingdom. All in all, this GCP training is ideally suited for young and experienced professionals from NHS organisations, university hospitals, pharmaceutical companies, CROs, and research institutes within the United Kingdom.
 Introduction & The Principles of ICH GCP
 Informed Consent
 Ethics
 Investigator Responsibilities
 Sponsor Responsibilities
 Clinical Trial Protocol
 Investigator Brochure
 Essential Documents
 Safety Reporting
PURCHASE
 
COURSE DEMO
 
VISIT WEBSITE

ICH GCP in English
If you are looking for pure ICH-GCP training online, this course will present you with an accessible, comprehensive, and flexible way of achieving a GCP certificate, which is endorsed by the Faculty of Pharmaceutical Medicine of the Royal College of Physicians of the United Kingdom. The course covers all the changes/amendments proposed in the EU Directive 2005/28/EC. In addition, the Summary of Proposed Changes to current regulations is attached for ready reference and those changes are also included in all relevant chapters of the course.
 Introduction & The Principles of ICH GCP
 Informed Consent
 Ethics
 Responsibilities of Investigator
 Responsibilities of Sponsor
 Clinical Trial Protocol
 Investigator Brochure
 Essential Documents
PURCHASE
 
COURSE DEMO
 
VISIT WEBSITE

ICH GCP adapted for the US in English
The US version of the GCP online training is in line both with ICH-GCP standards and regulations, as well as FDA regulations relating to them. This solution is suitable to both young and experienced clinical professionals involved in clinical trials in the United States, such as investigators, CRAs, monitors, ethics committee members, research nurses, and university students. Accessible, comprehensive, and flexible, it gives the opportunity to avoid more costly and time-consuming alternatives to obtaining an ICH-GCP certificate.
 Introduction to US GCP
 The Principles of ICH GCP
 Informed Consent
 Ethics
 Investigator Responsibilities
 Sponsor Responsibilities
 Clinical Trial Protocol
 Investigator Brochure
 Essential Documents
PURCHASE
 
COURSE DEMO
 
VISIT WEBSITE

ICH GCP adapted to Germany in German
The German version of the GCP Online course provides an updated and detailed overview of the principles of Good Clinical Practice according to ICH-GCP and presents the national requirements in Germany, which are included in the German Medicines Law and the German GCP Guideline. The training was customized for the German audience by one of the most recognized names in the industry - Dr Reiner Lehmann. It is perfectly suitable for every professional involved in clinical trials in Germany and covers all the requirements of the inspectional institutions. The German online GCP training is the quickest and most convenient way to obtain a recognized GCP certification and gain the GCP knowledge required for professional practice in the field of Clinical Research for our current and future German speaking customers.
 Einleitung und Grundsatze der ICH GCP
 Einverstandniserklarung
 Ethik
 Zustandigkeiten des Forschers
 Zustandigkeiten des Auftraggebers
 Bericht von den klinischen Studien
 Broschure des Forschers
 Wichtigste Unterlagen
PURCHASE
 
COURSE DEMO
 
VISIT WEBSITE

ICH GCP in Spanish
This Spanish-language version of the International ICH-GCP online training is designed to facilitate Spanish-speaking clinical research professionals from Europe, Central and South America. Like the English original, it presents an accessible, comprehensive, and flexible means to achieving a GCP certificate. It is endorsed by the Faculty of Pharmaceutical Medicine of the Royal College of Physicians of the United Kingdom and covers all the changes/amendments proposed in the EU Directive 2005/28/EC. In addition, the Summary of Proposed Changes to current regulations is attached for ready reference and those changes are also included in all relevant chapters of the course.
 Introduccion y principios de ICH GCP
 Consentimiento informado
 Etica
 Responsabilidades del Investigador
 Responsabilidades del Promotor
 Protocolo del ensayo clinico
 Folleto del Investigador
 Documentacion relevante
PURCHASE
 
COURSE DEMO
 
VISIT WEBSITE

ICH GCP in Polish
This Polish-language version of the International ICH-GCP online training is designed with Polish-speaking clinical research professionals in mind. Like the English original, it presents an accessible, comprehensive, and flexible means to achieving a GCP certificate. It is endorsed by the Faculty of Pharmaceutical Medicine of the Royal College of Physicians of the United Kingdom and covers all the changes/amendments proposed in the EU Directive 2005/28/EC. In addition, the Summary of Proposed Changes to current regulations is attached for ready reference and those changes are also included in all relevant chapters of the course.
 Wstep i zasady ICH GCP
 Zgoda poinformowana
 Åtyka
 Odpowiedzialnosc badacza
 Odpowiedzialnosc zleceniodawcy
 Sprawozdawczosc badan klinicznych
 Broszura badacza
 Najwazniejsze dokumenty
PURCHASE
 
COURSE DEMO
 
VISIT WEBSITE

ICH GCP in Russian
This Russian-language version of the International ICH-GCP online training is intended for clinical research professionals from the vast Russian-speaking commonwealth. Like the English original, it presents an accessible, comprehensive, and flexible means to achieving a GCP certificate. It is endorsed by the Faculty of Pharmaceutical Medicine of the Royal College of Physicians of the United Kingdom and covers all the changes/amendments proposed in the EU Directive 2005/28/EC. In addition, the Summary of Proposed Changes to current regulations is attached for ready reference and those changes are also included in all relevant chapters of the course.
 Введение и основные принципы проведения ICH GCP
 Информированное согласие
 Этические принципы
 Обязанности исследователя
 Обязанности спонсора
 Протокол клинических исследований
 Брошюра исследователя
 Основные документы
PURCHASE
 
COURSE DEMO
 
VISIT WEBSITE

Classroom Training Solutions for the United Kingdom
PharmaTraining is a joint effort by the renowned Dr. Laura Brown and Infonetica Ltd., which combines their expertise and experience in delivering training solutions for the pharma industry. You will find up-to-date, expertly-designed and professionally-performed classroom and online training courses, and seminars for all types of organizations and professionals operating in it.
 Good Clinical Practice Skills
 Pharmaceutical Technical Skills
 Management/Personal Development Skills
 Support staff courses include
 Course assessment etc
 Consultancy
 Custom Tailored Solutions
PORTFOLIO
 
VISIT WEBSITE



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