Resources

Aperio Clinical Outcomes
General Overview

Aperio provides full, customizable clinical research services across multiple therapeutic areas. More important, we offer what pharmaceutical and biotechnology customers need most in today’s world of healthcare: intelligence, honesty and agility. We deliver comprehensive clinical research services with unmatched transparency.

Select the Best eTMF System for Your Clinical Trials

Are you considering an eTMF implementation for your organization? Do you need a more efficient process to track and store your clinical trial documentation?

Watch a recent presentation “Why Switch to Medidata eTMF” from Medidata NEXT 2018 with Aperio’s Melissa Hancock and Medidata’s Paul Tilley, as they provide an overview of how to select the best eTMF system for your clinical trial. During the presentation, you will learn about the multiple eTMF vendor options available; what is required as a sponsor for system validation; and about the various integration options with EDC/CTMS systems.

Begin With the End in Mind: Are You Ready for First-in-Human Clinical Trials?

You’ve been moving steadily from discovery into preclinical, and based on the data, your molecule will be advancing into First-in-Human clinical trials. But with funds limited, resources tight and many conflicting priorities, how do you know where to begin to make sure your organization is ready for clinical trials?

Watch our presentation moderated by Aperio COO Suzanne Kincaid along with her distinguished line-up of panelists from Nuventra Pharma Sciences, SpringWorks Therapeutics and G1 Therapeutics to learn what your organization needs to do to prepare for First-in-Human

Begin With the End in Mind: Top 5 Considerations on Your Critical Path to First-in-Human Clinical Trials

You have been moving steadily from discovery into preclinical, and based on the data, your molecule will be advancing into First-in-Human clinical trials. Congratulations are in order ─ but with limited funds, tight resources, and a myriad of conflicting priorities, how do you begin to make sure your organization is ready
for clinical trials?

To help you prioritize what is most important, we have summarized the top five most important considerations on your critical path to FIH clinical trials.

Clinical Research Outsourcing: Building Strong CRO Partnerships

Trends indicate that nearly every company developing drugs and medical devices has to outsource something, especially if you are not Top 50 Pharma. But how do you know what services to outsource and to whom? Which clinical trial services are critical to keep in-house? How much oversight should you maintain? What are the secrets to a successful partnership?

Watch our presentation and learn from our moderator, Suzanne Kincaid, COO for Aperio, and her panel of industry experts in clinical development about how to choose the right partner; document your oversight and make outsourcing easier; and ensure your partnerships are successful.

Clinical Research Outsourcing Video Series

Clinical outsourcing is inevitable if you are a small biotech or medical device company. But with so much at stake, how can you ensure that you select the right clinical research outsourcing partner? What tools and process are helpful when you’re comparing vendors? What are the pitfalls you need to avoid? And what does it mean to demonstrate oversight of your clinical study?

Watch our short video series on Clinical Research Outsourcing and find the answers to these important questions and more.

The Benefits of a Flexible Database Design for Today’s Complex Clinical Trials

Clinical trials have become more complex than ever. Whether it is planning for multiple Investigational Products (IPs), incorporating an adaptive study design, or managing multiple protocol changes, it is important to implement a database design upfront that will allow for downstream changes to be made to the database quickly, efficiently, and with minimal impact to the existing data.

Watch this presentation from Mediata NEXT 2019 featuring Aperio’s Brian Stoddart and Acerta Pharma’s Herminio Sinoy, as they discuss how flexible database designs present a proactive solution for managing complex trials.

Considerations of Designing Your Virtual Trial: Lessons Learned from Data Management

Data collection and reporting for clinical studies is evolving through implementation of new technologies that allow for direct patient data collection and access to electronic medical records. While these technologies offer numerous benefits, the processes we develop to encompass them are often overly restrictive and don’t allow for creativity or intuitive solutions and tools to help us achieve our goal.

Watch this presentation from Medidata NEXT 2019 featuring Aperio’s Stacey King and Medidata’s Michael Tucker and Naima Gibson, as they discuss getting the maximum benefit from patient data collected from personal devices and why uniformity and standardization is critical.

VIDEO SERIES

Medical Device Development Video Series

Whether it is to support a Premarket Approval (PMA), 510(k), or post-market strategies, your clinical trial is a crucial next step in the life of your medical device.  Understanding the multiple facets necessary to consider in the clinical development process will provide you with a holistic view of the road ahead, and allow for realistic short- and long-term planning for your device development and commercialization.

Watch our short video series on Medical Device Development and discover how to prepare for your medical device clinical development program.