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Partnering To Advance Your Mission

At RLS, we understand that we protect not just data but we protect patients. Partnering with our team takes the stress and ambiguity out of voluntary and regulatory data sharing. Contact us today to discuss your regulatory disclosure or voluntary data sharing project.
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We're Here To Help...As Much Or As Little As You Need

Real Life Sciences can tackle entire projects or collaborate with your team to fill in the gaps as needed. Whether it's clinical trial disclosure submissions for Health Canada PRCI or EMA, or voluntary data sharing projects, you can depend on our deep expertise and breadth of experience to deliver success.


Turnkey Project Management

Our Project Managers bring a fresh perspective — leveraging technology, years of experience, methodology, and a gift of communication. RLS works side-by-side with you and your team in each stage of the process, from pre-planning to proposal to final submission. Your success is our success. Some of the requests we hear:

  • Hard deadlines imposed by regulators
  • Therapy development timelines
  • Need for increased efficiency

Your Timelines. Your Team.

Your Extended Resources

After we discuss your project and your timelines/deadlines, we will mutually construct a team to meet your needs. You will find Real Life Sciences is laser focused on your success. You can opt for:

  • Dedicated Resources
  • Pooled Resources
  • A team built for your needs and your timelines.

Repeatable Processes

Long Term Success

Many sponsor teams we work with have a recurring need. That means either treatment pipeline disclosures over time or voluntary disclosures that will be required on multiple occasions. We provide your team with a tried and tested way to move forward based on our SaaS solutions. The team at Real Life Sciences uses our solutions every day, so we can set your team on a long-term path designed for success.

  • Refined systems that your team can implement to improve efficiency
  • Training on methodology and regulatory expectations
  • SaaS training to enable your team fly solo

We Can Be Your Guide

Knowledge and Experience

Leverage our deep knowledge of regulations and extensive experience gained working with top Pharma organizations. Every RLS Anonymization Service team member undergoes a thorough training before they are put on a project. Then they are paired with an experienced buddy to gain practical experience before they are put on a client project. This means you get a seasoned team every time.

Let us show you how RLS can help.

We’re with You, Every Step of the Way.

In any configuration you need, tap into our experience. We can work alongside your team to develop relocatable process that improve efficiency and deliver success.
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You know you have regulatory deadlines to meet and RLS Protect is your agreed upon solution . Now the rubber meets the road. How do you want to tackle your challenges to achieve successful results? We configure a managed service model that delivers for you.
While the RLS Anonymization Service team will be responsible for the day to day tasks of the project, we ensure that we work hand in glove with the sponsor to review and approve the anonymization strategy. 

The Anonymization Service team members are qualified pharmacists or nurses who have extensive medical writing and case processing backgrounds . Our dedicated risk team been extensively trained on regulations and the statistical methods of risk assessment to ensure that maximum data utility is retained while protecting patient privacy.

Typically, a sponsor will need representation from the Medical Writing, Legal, Regulatory, Trial Disclosure & Transparency teams to ensure that the final anonymized documents meet internal standards.

Absolutely! The RLS Anonymization Service team has experience with processing over 1 million pages and thousands of datasets for regulatory and voluntary submissions. In fact, we maintain consistent methodologies across deliverables so that rework is minimized when a voluntary submission has to be submitted to the regulators.

Yes! Depending on the volume and frequency of submissions, we can work with you to dedicate a team for your projects so that you always have a single project manager, risk lead and redaction lead to interface with. This allows consistency of methodology across projects as well.

Certainly! In fact, we recommend this approach. Most of our clients start working with us with a turnkey managed service model and then move to a SaaS model. We ensure that we partner with you throughout the implementation process as well as provide methodology and application training to ensure the success of your team. We also offer a robust support plan post implementation which includes new user and/or refresher trainings as well as general assistance as needed.

Partnering with you for preparing for the Process Initiation Meeting (PIM) is an inherent part of what the Anonymization Service model offers. In fact, most of our clients want us to attend meetings with regulators so that the methodology used is clearly explained and agreed to.