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Get to Your
ICH E6(R2) Goals Faster

Sponsors and CROs know they have to comply with ICH E6(R2) guidelines for taking a risk-based approach to clinical trials, but the vast majority don’t know how to align with the new directives.

Read the blog: 89% of Sponsors Say They Need Help Aligning with ICH E6(R2)

Comprehend has been talking about ICH E6(R2) since 2016, and we’ve compiled the most relevant content to help you achieve compliance faster.

To get started, choose your level of ICH E6(R2) involvement

 We’re just getting started with ICH E6(R2)

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We could use some advice on maximizing our alignment ICH E6(R2)

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We’re continuing to fine-tune our risk management and oversight strategies in the context of ICH E6(R2)

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Just Getting Started with ICH E6(R2)

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On-Demand Webinars

Need Advice on Maximizing ICH E6(R2)

Blog Posts

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On-Demand Webinars

Fine-Tuning Risk Management & Oversight Strategies

Blog Posts

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On-Demand Webinars

We’re Here for You!

As a trusted technology partner, Comprehend has been helping sponsors and CROs reduce risk and improve the performance of clinical trials since 2010.

Our Clinical Intelligence Suite delivers the latest innovations in data science to help you unify your clinical data, identify and resolve issues faster, and dramatically improve your audit readiness.

Because our solutions align with ICH E6(R2) guidelines for good clinical practice, we can get you on the fast track to compliance.

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Saama can put you on the fast track to clinical trial process innovation.

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Terms & Conditions

By inquiring about Saama’s Database Lock in a Day, you agree to be contacted by Saama and to allow Saama to use, maintain, store, and protect your personal data in accordance with our Privacy Policy.

Eligibility details are for informational purposes only. Saama, in its sole discretion, will determine your eligibility based on the information you disclose as part of the intake process. If Saama determines that you are eligible to participate, you will be notified by separate email. Eligibility depends on certain criteria, such as the size of your company, the types of clinical trials you sponsor, and the number of patients in–and stages of–your current clinical trials.

By completing the request form, you represent that you have authority to proceed on behalf of your company. Should you agree to participate, you agree to reasonably cooperate with Saama in following the guidelines and procedures required for integrating, standardizing, and analyzing your data. Participation requires the use of our Smart Data Quality application, a technology-agnostic AI engine that sits on top of your current infrastructure. The application can be used immediately, and you’re only charged for the services you use based on a predetermined estimate.

Information you share with Saama during your participation may be anonymized and/or aggregated, and made available publicly in Saama marketing materials. This information may include: types of systems and processes involved, types of departments involved, and size and regional location of your company. Such information will never be directly associated with you, nor will you or your company be identifiable without express written permission.