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GCP: ICH Good Clinical Practice (ICH-GCP) (GCP001)

Certification Training Duration: 2 hours (the average time to complete the training program, including final assessments).
Credits Hours: 2
CPD Accredited TrainingAccreditation: This training course offers CPD accreditation from the Faculty of Pharmaceutical Medicine of the Royal Colleges of Physicians.
CPD Credits: 3
Demonstration: Demo an online course.

Certificate: View sample certificate.

PRICE: USD $195.00 LogoTraining Program: GCP: ICH Good Clinical Practice (ICH-GCP)
Training Provided By:

Availability: Immediately available upon ordering.

Description: Online training with immediate access upon enrollment.

Many regulatory changes are happening in the pharmaceutical industry. Those who are particularly affected are individuals involved in research. When carrying out research duties, there is always the risk of breaching ethical codes and/or compromising the quality of generated data. Critical to ensuring credible, high-quality data and ethical research is an understanding of the principles and background involved in Good Clinical Practice. This online course discusses the structure and key principles of ICH GCP and provides a broad framework in which to apply the standards of Good Clinical Practice through the use of actual practitioner experience and accounts.

The class covers topics such as informed consent, investigator responsibilities, documentation, teamwork, ICH GCP, harmonization, monitor responsibilities, and a key point summary at the end.

Once all course requirements have been satisfied, a Certificate of Completion is immediately available. Course takers can attempt the final assessment any number of times, as needed, in order to achieve a passing grade.

Benefits of Getting Certified at

By employing advanced e-learning training techniques, and coupling them with new automated tracking systems, the provides professionally designed online courses which are effective at training, and assist those interested with advancing their careers. The also assists companies through maintaining training records, the education of their employees, and assisting them with improving their overall quality of service. By coupling new automated tracking systems with proven and advanced e-learning training techniques, the can do for you and your company what we have done for numerous companies – both abroad and within the USA. We can assist in the maintaining of training records, the education of your employees, and with an overall improvement in the quality of service you offer.

Have Questions?

Should you have any particular question about this course, you can call us at (888) 111-1111 or send us an email at for more information.

Certification Requirements: Students must view the entire program and successfully pass an online, multiple-choice final assessment with >80% passing grade within a 90 day period of time (180 days for Professional Certification Programs). Certificate is accessible in PDF format immediately after satisfying requirements.

Online Training Programs Include:

  • Immediate access to training: Instructions, password, and username are emailed following order
  • 90 days of 24/7 access to individual training programs / 180 days for Professional Certification Program
  • Programs include voice-overs, easy navigation, progress checks, and high-quality animations
  • Course notes (in PDF) and/or references available with select training programs
  • Online final assessment with multiple-choice questions can be taken an unlimited number of times, until passing grade is achieved
  • A Certificate of Completion is immediately available once course requirements have been satisfied

The GCP: ICH Good Clinical Practice (ICH-GCP) Course is Found in the Following Professional Certification Program(s):

Clinical Trials Management Professional Certification Program: This professional certification program is designed for clinical managers, project managers, and clinical research associates and coordinators, or those with desire to grow their career into these positions. Co … Learn more

Good Clinical Practice Professional Certification Program: This online professional certification program is for clinical managers, project managers, investigators, and clinical research associates and coordinators, or those with the desire to grow their career into th … Learn more


Harmonization: The topics covered in this session map the development of ICH and the processes involved in establishing international standards and the technical requirements to ensure the safety, quality and efficacy of new medicines.

ICH GCP Guidelines: The topics covered in this session describe the principles and structure of ICH GCP and provide a broad context in which to apply the standards of good clinical practice.

Teamwork: This session examines the roles of the sponsor, investigator and monitor and the communication and interaction necessary to fulfill these obligations and conduct a successful trial.

Documentation: This session connects these key documents with the responsibilities of the investigator, sponsor, monitor and support team.

Investigator responsibilities: This session covers the main responsibilities of the investigator for the conduct of the clinical trial and explains how to ensure the accuracy, completeness, legibility and timeliness of data generated during the study.

Informed consent: This session focuses on the main requirements necessary to support an effective and efficient informed consent process.

Monitor responsibilities: This session explores the responsibilities of the monitor and provides insight into these key challenges.

Summary: Key point summary for all topics covered in This online course. Ideal for review, a refresher or consolidation of learning points.


Students completing this course should be able to:

–Understand the processes involved in establishing international standards and technical requirements for Good Clinical Practice.

–Describe the principles and structure of ICH GCP.

–Apply the main guidelines of Good Clinical Practice in the workplace.

–Explain the key responsibilities of the Sponsor, Investigator, Monitor and the Study Team in conducting a successful clinical trial.

–Understand the use of key documentation used in clinical trials.

–Demonstrate an understanding of the informed consent process in clinical trials.


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