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Good Clinical Practice Certification

PharmaEduCenter
Best Good Clinical Practice Training & Certification Online

Having worked with clinical sites for over 20 years in the pharmaceutical industry,
we are now offering you access to all of the key secrets of clinical research.

Self-paced online learning

Study at your own pace with interactive virtual modules. Your progress is automatically saved, so you can start and stop whenever you like.

Real Life Case Studies

Our courses include real-life case studies and scenarios, helping you relate training content to your daily practice.

Certified Content

Our GCP Courses comply with regulatory requirements so you can ensure you have been adequately and effectively trained on Good Clinical Practices.

Accreditation

Our Good Clinical Practice training meets the criteria for ICH GCP Investigator Site Personnel Training identified by TransCelerate BioPharma, so you will not need to retake the GCP training as it is recognized by most trial sponsors

For Individuals

Clinical research professionals can get Good Clinical Practice Certification from us. Before starting a clinical trial, principal investigators and site staff must complete GCP training and refresh it every three years.

For Institutions

We provide Good Clinical Practice Certification to working teams. Our training meets the tough demands of the clinical research and pharmaceutical sectors. We offer discounts for multiple purchases and corporate clients.

Get your Good Clinical Practices Certification today!

Check out our trainees testimonials

Good mix of theory and practice. The realistic case studies exceeded my expectations, helping me to rethink typical situations on the daily work.
Carolina Hurtado
Investigator
"Easy to use with excellent content. The course is simple to follow and provides a comprehensive overview of GCP. I really enjoyed how interactive the course is. In a couple of hours, I obtained my GCP certificate. Thank you."
Anonymous
Investigator
"I do prefer the e-learnings as this was easier to combine with my job, the time savings were also nice because I didn’t have to attend a face to face course… The lessons were very interactive and the study cases really interesting."
Zasha Sweny
CRA

Go beyond the basics with our comprehensive and practical ICH GCP training

Good Clinical Practice Certification

What is GCP Good Clinical Practice in Research?

ICH GCP Good Clinical Practice Guidelines are international ethical and scientific standards for the design, conduct, performance, monitoring, auditing, recording, analysis, and reporting of clinical trials. The goal of GCP is to ensure the protection of the rights, integrity, and confidentiality of clinical trial participants and to ensure the credibility and accuracy of data and reported results.

It is required for the (principal) investigator and staff involved in the conduct of GCP clinical trials, to have completed GCP training before start of a clinical research. An Ethics Committee will not approve a clinical trial if the (principal) investigator does not have a valid GCP training certificate, including an ICH GCP test.
Besides, every 3 years, a GCP refresher training should be retaken.

PharmaEduCenter’s online GCP courses meet the identified GCP training minimum criteria for investigators and site personnel, and are added to the list of providers and accepted GCP training courses. As a result, our GCP course is acknowledged and accepted by all pharmaceutical companies affiliated with TransCelerate. You will no longer be required to complete a duplicated GCP course.

  • GCP principles ensure that clinical trials are conducted in an ethical and scientific manner. It provides guidelines for clinical trial design, conduct, performance, monitoring, auditing, recording, and reporting.
  • Any person working in clinical research or any organization conducting clinical trials with human participants must comply with the GCP guidelines and should have a Good Clinical Practice Certification.
  • We offer the most advanced Good Clinical Practice training recognized by Transcelerate Biopharma.

Good Clinical Practice Certification

The benefits of having a Certified workforce

In clinical research, having a workforce with GCP certification is invaluable. Good Clinical Practice, or GCP for short, is the norm that clinical trials have to follow to guarantee compliance and safety. This applies not only to CROs and Sponsors, but also to clinical trial sites.

  • Employing personnel with an ICH GCP certification can save CROs or Sponsors a lot of money and lead to better patient outcomes, reduced clinical trial errors, enhanced regulatory compliance, and higher trial performance.
  • The availability of skilled personnel who understand good clinical practice standards will enable CROs to acquire new protocols much more quickly and easily.
  • Ensuring safe and ethical clinical research that complies with regulatory standards requires a workforce with GCP certification. Proper practices lead to lower failure rates and costs.
  • Clinical trial sites that have received GCP training for every member of their staff are typically qualified, approved, and initiated faster.

FAQs

GCP training is required for research teams involved in clinical trials of drugs, biologics, and devices research studies.

  • ICH E6 (R2) GCP Essentials for investigators and site personnel and Buenas Practicas Clinicas para Investigadores y centros (ICH GCP E6 R2): are both suitable to train clinical investigators and site personnel (in English and Spanish, respectively) on the fundamentals of GCP and how to apply them practically in the research setting. It is also ideal as a GCP refresher, as it meets the minimum criteria for ICH GCP Investigator Site Personnel Training identified by TransCelerate BioPharma, Inc. as necessary to enable mutual recognition of GCP training.
  • ICH GCP E6 (R2) Good Clinical Practice training: is suitable to train clinical research professionals (those working in the Pharmaceutical Industry and CROs, as for example, CRAs/Monitors) that need a more comprehensive knowledge of ICH GCP. This GCP training is also ideal for people just starting or willing to start working in the Pharmaceutical industry, CROs or Clinical Sites, as it provides comprehensive and practical  knowledge of the ICH GCP Guideline.  

This will depend on the course; nevertheless, learners may complete the modules at their own pace

GCP training for Investigators will approximately take around 2.5 hours to complete, as it is mainly focused on Investigator’s responsibilities.

Full GCP course will take around 6 hours to complete. 

There is no uniform standard regarding how frequently GCP training should occur. However,  regulatory authorities and auditors/inspectors usually require Good Clinical Practice training to be refreshed every 3 years. Please check your country’s regulations.

A quiz is also required in order to obtain the Good Clinical Practice Certification. Usually, the passing score is greater than or equal to 80%.

Yes, our 3 GCP courses are mutually recognized by TransCelerate BioPharma. You could review each course in detail on the COURSE page.

Yes. When you complete a GCP training course with PharmaEduCenter, you will receive an electronic copy of the certificate, which you can print. This will include information about the course you took as well as the date you completed it. You can then save this for your records.

Yes, at the end of each GCP course there is a quiz you will need to pass in order to demonstrate you have acquired the knowledge and are appropriately trained. The passing score is greater than or equal to 80%.

Although we cannot guarantee you a job if you enroll in our GCP courses, we believe that by doing so, you are providing yourself with a great opportunity to advance in your career by expanding your knowledge and skill set and staying current with industry developments. Furthermore, upon course completion, you will have the option to print the GCP course certificate, which includes all the reviewed topics.

You should include your GCP training in your work portfolio to demonstrate your knowledge to prospective/current employers.

If you sign up for our newsletter, you will see discounts being sent out periodically for single users.

We offer discounts for more than five accounts, so please get in touch with us to discuss a discount if you need to buy a course for multiple users.

Yes, please contact us to discuss your team needs.

When you select a GCP course, the system will allow you to start for free. Then, if you want to move forward with the course, you will need to create an account and purchase it. You can pay online via our secure Stripe’s payment gateway, using your preferred card, at no extra cost. 

If you have a discount code, you must complete the course registration process as usual. Then, when you get to the screen where you have to enter your information and make payment, there will be a field where you can enter a discount code, if any. If the code worked, the course’s price will be updated to reflect the new discounted price.

Then, proceed to sign up as usual, entering all of your information.

It means that it is flexible enough to allow you to start and stop from any device whenever you like, and the system will automatically save your progress. You will have 3 months to complete your GCP certification.

Although they are both vital to the development of medicine, clinical and medical research have different goals and purviews.

Any research that attempts to deepen our understanding of human health and disease is included under the broad category of medical research. Among other sorts of studies, it might include population-level research, epidemiological studies, or simple laboratory research. Identifying the underlying causes of disease, creating new diagnostic instruments, or investigating novel treatment approaches are all common goals of medical research.

Contrarily, clinical research is a branch of medical research that focuses on investigating novel medications, therapies, or interventions in human subjects. Clinical research can involve conducting clinical trials to test novel medications, medical devices, or procedures. It frequently entails conducting meticulously controlled studies to evaluate the side effects, efficacy, and safety of these interventions.

If a person is interested in investigating more general issues regarding human health and illness, such as comprehending the underlying mechanisms of a disease or determining risk factors for a specific condition, they may opt for medical research over clinical research. On the other hand, if a person is eager to test a novel intervention on humans in order to ascertain its efficacy and safety, they might opt for clinical research.

For the purpose of expanding our knowledge of human health and disease and enhancing medical treatment, both clinical and medical research are essential. Together, these complimentary methods enhance patient outcomes and progress medicine.

Yes, we keep track of all of our users and the dates on which they took our course. You, or your employer, may contact us at any time to confirm the validity of your certificate.

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