Investigator Training Portal

Drive compliance and knowledge within your clinical program

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Level Up Your Investigator Training

Qualifying, selecting and monitoring a global provider of site training for your clinical trial is not as straightforward as it may seem. Here are some criteria that you need to review in order to select a provider that will get you ahead of the game and keep your investigators motivated.

 

  • Ensure data quality and inspection readiness
  • Leverage efficiency and increased collaboration
  • Enhance site engagement and retention of trial knowledge

Learn more here.

 

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GCP Learning, Easily Embedded In Your Workday

Anytime, Anywhere Training

Your staff and sites shouldn’t have to spend time in a classroom bringing their GCP training up to date or waste valuable time with delays with the ethics committees due to non-compliant training.

Cost Effective, Plug & Play Learning System
Continuous Regulatory Compliance & Reminders
Learn Conveniently: Whenever and Wherever

Our innovative learning system is suitable for CTAs, CRAs, investigators, site, and clinical staff.

Single Training Hub for Site/ Trial Teams

Reduce study start up time due to redundant training. Our single, study branded standardized training portal gives sites access to training.

Virtual Investigator Meetings
Site Initiation
Protocol Specific Training

Ensure better data quality in sponsor systems, and increase collaborations with sites and CROs.

Get Full Inspection Readiness

Monitor GCP compliance with comprehensive training records at your fingertips. Improve trial and data quality with continual, up-to-date GCP training. 

Monitor and Document Training Compliance
Streamlined Processes for Regulatory Compliance
Automated Regulatory Update Reminders

Ensure your sites and staff are audit and inspection ready and increase efficiency in compliance data assessment.

What Others Say

“GCP certification via GCP Central, a Seuss+ partner. Online, at your own pace and with clear explanations.”

 

“A prestigious e-learning development project, including implementation, hosting of the DCRF Academy (powered by myGCP) to provide all research professionals in The Netherlands with a engaging training on the new EU Clinical Trials Regulation.”

Hans Stam, DCRF Board Member

“Provide continuous online GCP training to all study site personnel and investigators of the Vascular Research Network (VRN) in the Netherlands via a dedicated learning platform including a customized registration process for VRN.”

P. Kastelein, VRN

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