Blog

Introducing Fireside Chats: Conversations On Burning Research Topics

July 2, 2020

Advarra is excited to introduce Fireside Chats, a series of virtual conversations discussing current issues in clinical trials. Each Fireside Chat brings together perspectives from across the research community, enabling…

Webinar

COVID-19 Lessons Learned: Technology and Agility in the New Clinical Trial Landscape

Clinical trials research was forced to evolve and embrace technology in the wake of the COVID-19 pandemic. This unprecedented crisis created a necessary disruption in the use of technology to…

Blog

Q&A Part 1 – Evaluating Payment to Participate in Research: Ethical and Regulatory Issues

April 15, 2020

In a recent webinar, Dr. Luke Gelinas, IRB Chair at Advarra, provided a framework for evaluating offers of payment to research participants. In addition to outlining the challenging ethical and…

Blog

Protocol Feasibility to Promote Trial Efficiency

April 15, 2020

Scientific abstracts and articles have reported that 20-50% of studies do not accrue subjects at the site level (1-6). This contributes to a significant amount of waste in clinical research,…

Blog

Study Activation: A Complex Process That Doesn’t Have to Be Painful

April 15, 2020

Study activation data from the Forte community shows on average, it takes about six months to activate a new, interventional, treatment clinical trial. Long activation periods are not a new…

Webinar

How Sites and Sponsors are Collaborating to Move eSource Forward

In this webinar, Shannon Roznoski, Director of Product Management at Advarra-Forte and Michael Buckley, Manager, CRIT Enterprise Innovation at Memorial Sloan Kettering Cancer Center will discuss their experience as members…

Webinar

Evaluating Payment to Participate in Research: Ethical and Regulatory Issues

Luke Gelinas, IRB Chairperson at Advarra, proposes a practical framework for evaluating offers of payment and applies it to case studies to yield guidance on challenging ethical and regulatory issues…

Case Study

Part 11/Annex 11 Independent Audit and Compliance Assessment

February 28, 2020

Independent verification of compliance opens new doors for CRIO, Inc. and provides customers confidence that they can incorporate the eSource system into their own computer software validation strategy.

Case Study

Advarra Integrates IRB with Veeva Vault eTMF, Delivers Unparalleled Efficiency for a Top 10 Biopharma

February 28, 2020

Teamwork and leadership from an industry-leading biopharmaceutical company and Advarra accomplish integration through Veeva Vault eTMF, saving over 8000 hours in the first 6 months.

Blog

Advarra Acquires Forte:
What You Need to Know

September 5, 2019

On September 5, 2019, Advarra announced its intent to acquire Forte. The combined organization leverages mutual strengths in supporting the research community with client service, regulatory expertise, and technology-enabled efficiencies…