Websites targeting keyword ich-gcp

Badania kliniczne, GCP, ICH, ICH-GCP, CRO, szkolenie GCP. Strona Polskiego Związku Pracodawców Firm Prowadzących Badania Kliniczne na Zlecenie.

GCP online training course provides a comprehensive guide to the basic principles, regulations and guidelines of ICH Good Clinical Practice, for conducting clinical trials and researches

国内外の製薬会社での豊富な実務経験を有するスタッフが、お客様の様々なニーズにフレキシブルかつ迅速に対応し、高品質なメディカルライティング・コンサルティングサービスを提供します。。

Offering in person, onsite and online accredited technical training. Browse CfPA's technical training courses for pharmaceutical, biotechnology, food, chemical, medical device, and cosmetics

International Conference on Harmonisation of technical requirements for registration of pharmaceuticals for human use. A standard for the design, conduct, performance, monitoring, auditing, recording, analyses, and reporting of clinical trials that provides assurance that the data and reported results are credible and accurate, and that the rights, integrity, and confidentiality of trial subjects are protected. Ethical and scientific quality standards for designing, conducting, recording and reporting trials that involve participation of human subjects to ensure that the RIGHTS, SAFETY and WELLBEING of the trial subjects are protected. Ensure the CREDIBILITY of clinical trial data. ICH GCP (E6): TABLE OF CONTENTS

GCP (Good Clinical Practice) online training course. The training course is endorsed by the Royal Holloway, University of London and carries 9 CPD (Continuous Professional Development) points.

Whitehall Training specialises in providing clients with Good Clinical Practice Training. We offer affordable GCP, Pharmacovigilance and other courses around the world

Clinical Research Technology è una struttura di ricerca a contratto dedicata alla gestione di studi clinici secondo gli standard di Buona Pratica Clinica (GCP-ICH) tramite l’utilizzo estensivo delle nuove tecnologie informatiche ed Internet in particolare Clinical Research Technology is a company oriented to the management of clinical trials according to Good Clinical Practice standards and respecting its own and the Customer’s SOPs (constantly updated and monitored)