ICH GCP Login

Listing Results ICH GCP Login

About 19 results and 6 answers.

Login - ICH GCP Training Course

12 hours ago Note. If you select the 'Remember me' option, you should not log out at the end of your session but simply close the web browser. When you return to GCP training site you will already be logged in, so you will not need to enter your user name and password. You can turn off this feature by clicking the Log-out tab at the top of the screen.

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Good Clinical Practice

2 hours ago This training has been funded in whole or in part with Federal funds from the National Institute on Drug Abuse, National Institutes of Health, Department of Health and Human Services, under Contract No. HHSN27201201000024C.

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GCP online training course - Login - ICH GCP (Good

11 hours ago Login to your account. Important: Please be sure you have logged out every time you access the GCP site from a public computer, otherwise someone else could use your account. If you have any queries regarding your purchase please contact Uxia Fernandez by email or phone + (44) 207 0997432.

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ICH GCP - ICH harmonised guideline integrated

6 hours ago 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 ...

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gcp.nidatraining.org - Good Clinical Practice

7 hours ago The Good Clinical Practice (GCP) course is designed to prepare research staff in the conduct of clinical trials with human participants. The 12 modules included in the course are based on ICH GCP Principles and the Code of Federal Regulations (CFR) for clinical research trials in the U.S.

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Google Cloud Platform

11 hours ago Google Cloud Platform lets you build, deploy, and scale applications, websites, and services on the same infrastructure as Google.

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E6 Good Clinical Practice: Integrated Addendum

8 hours ago This ICH GCP Guidance Integrated Addendum provides a unified standard for the European Union, Japan, the United States, Canada, and Switzerland to facilitate the mutual acceptance

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Good Clinical Practice CITI Program

3 hours ago Yes, after the ICH Integrated Addendum to ICH E6(R1): Guideline for Good Clinical Practice E6(R2) was adopted on 15 December 2016, the CITI Program modules were revised to reflect the current guideline. The GCP courses that reference ICH E6 specifically refer to the current guideline. CITI Program also offers some additional resources on ICH E6 ...

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Online Clinical Research Course

11 hours ago CCRPS offers accredited, affordable, in-depth on-demand clinical research certification for clinical research associates, clinical research coordinators, drug safety, ICH GCP, and clinical research assistants. CCRPS is ACCRE accredited and Joint accredited by the ANCC, ACCME, ACPE, and IPCE to provide CME credits.

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ICH GCP Certification I Accredited, Online I $50 Tuition

4 hours ago ICH GCP Training. Advanced ICH GCP Certification (AGCPC) The most advanced ICH GCP training available I 50 Hours I On-Demand I Biopharma Recognized I 15+ Modules I Images, Checklists, Application I Instant Enrollment I 1+ Day Certification. Select a pricing option $50.00 2 x $25.00. Purchase Free Preview.

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GCP ICH Refresher CITI Program

4 hours ago GCP Refresher - International Conference on Harmonisation (ICH): GCP Requirements. Provides a basic understanding of the ICH’s role and impact on conducting clinical research according to GCP. It describes the purpose of ICH and identifies the basic requirements for compliance with ICH GCP. Recommended Use: Required.

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ICH GCP - Review of ICH GCP guidelines and ICH GCP course

9 hours ago ICH GCP Guidelines. The ICH GCP guidelines, including ich gcp e6, provides public assurance that the rights, security and also well-being of trial subjects are protected in accord with the principles which have their source in the Declaration of Helsinki. In addition, compliance ensures credible clinical trial data.

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Clinical Research Certification - CCRPS Clinical Research

6 hours ago clinical research Training In-depth Courses. Global Compliance. Improve Job Prospects & Trial Outcomes. CCRPS provides affordable, industry-recognized, accredited, advanced ICH GCP training, CRA certification, CRC certification, research assistant training, pharmacovigilance certification, PI training, and clinical research project manager training for clinical professionals including nurses ...

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ICH-GCP: Good Clinical Practice, An Abridged Course

4 hours ago ICH-GCP: Good Clinical Practice, An Abridged Course. Rated 4.13 /5. 16 reviews. Program/Course ID: GCP00. Enrollment Period: 6 months. Average Learning Time: ~15 minutes. Method of Training: Online / Self-paced eLearning. Accessibility: 24/7 access to all program materials. Credit Hours: 0.5 credits.

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Training ClinicalResearch.com

3 hours ago This interactive, user-friendly training is TransCelerate Mutually Recognized and incorporates the latest guidance from the International Council for Harmonisation (ICH) (E6, R2). The core program includes 7 general ICH/FDA GCP modules, with 2 optional modules for sites in South Africa (module 8) and for training about applying GCP in ...

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Foundational ICH-GCP E6 Training - eLearning - ECCRT

4 hours ago ICH-GCP is the guideline ruling all clinical research including its conduct, performance, monitoring and reporting of the results. This eLearning course focuses on the requirements of Good Clinical Practice (GCP) in clinical studies with pharmaceuticals.

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Electronic Source Data in Clinical Investigations and

2 hours ago Page 1 Electronic Source Data in Clinical Investigations and Regulatory Expectations Kassa Ayalew, M.D., M.P.H. Branch Chief Division of Clinical Compliance Evaluation

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Frequently Asked Questions

  • What are ICH guidelines?

    ICH Guidelines means the guidelines of the International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use, providing for a unified standard for Canada, the European Union, Japan and the United States with respect to the interpretation and application...

  • What does Ich stand for in clinical research?

    Intracerebral Hemorrhage (ICH) Research and Clinical Trials. Intracerebral hemorrhage (ICH) is the most devastating type of stroke for which there are no proven effective treatments other than conservative management and supportive care. ICH is defined as a sudden bleeding episode in the brain tissue or ventricles.

  • How long is the ICH Clinical Practice Course?

    The 12 modules included in the course are based on ICH GCP Principles and the Code of Federal Regulations (CFR) for clinical research trials in the U.S. The course is self-paced and takes approximately six hours to complete.

  • What is the Good Clinical Practice course?

    The Good Clinical Practice (GCP) course is designed to prepare research staff in the conduct of clinical trials with human participants. The 12 modules included in the course are based on ICH GCP Principles and the Code of Federal Regulations (CFR) for clinical research trials in the U.S.

  • Is the ICH Guideline for GCP E6 applicable to clinical trials?

    Although the ICH Guideline for GCP E6 (ICH GCP) primarily relates to clinical trials and has an international context, all human research conducted in Australia should be undertaken in accordance with the GCP principles contained in the National Statement on Ethical Conduct in Human Research and ICH GCP (where relevant).

  • Is the National Institutes of Health providing GCP training?

    The National Institutes of Health (NIH) in fulfillment of their GCP training policy (Policy on Good Clinical Practice Training for NIH Awardees Involved in NIH-funded Clinical Trials; NOT-OD-16-148) states that NIH-funded investigators and staff should be trained in GCP.

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