Hot Topics Discussed in Covance Spring Webinars

Unlock opportunities for your clinical research programs and deliver results that Covance Spring Webinars Video Nash Diabetic Heart Biomarkersmatter.
We’re excited to be on the cutting edge of drug development solutions. Take a look at past and future webinar topics and leverage our experience.

Kidney Biomarkers in Drug Development

Experts discuss emerging translational biomarkers and insights into evaluation of nonclinical urine biomarker data.  We’ll also discuss translational biomarkers in clinical trials for recent renal-related diseases/mechanisms.

April 26, 11 a.m. EDT | Register now


Rare and Orphan Diseases Patient Perceptions
Implications for Recruitment, Retention and Compliance in Clinical Trials

Do you face the challenge of recruiting and retaining rare disease patients for orphan drug clinical trials? Now, discover how you can boost participation, enhance outcomes and speed drug development in this competitive market. Join Dr. Rolando Gutierrez-Esteinou, MD, Vice President, Therapeutic Area Head, Neuroscience Medical and Scientific Services at Covance, for this timely Webinar.

May 4, 11 a.m. EDT | Register now


Turning Biorepositories into Translational Science Treasure Troves: The Value of Uniquely Complete Data Sets

As clinical trials incorporate wider patient populations around the globe and the number of biomarker assays available increases, your specimen biorepositories represent an increasingly valuable resource for translational science. Learn how to get more value from your biorepository specimens by transcending data silos and gaining pan-pipeline insights to help you bring fresh approaches to your research.

May 4, 11 a.m. EDT | Register now


Implementing Basket/Bucket and Umbrella Designs: What You Need to Know for Global Oncology Trials

Recent successes in the treatment of cancer have led to more complex trials. Join our experts to learn more about the challenges faced in executing oncology trials and gain new insights on how to optimize your backet/bucket and umbrella designs.

May 8, 11 a.m. EDT | Register now


Biomarkers and Immuno-oncology: Identifying New Opportunities for Precision Medicine

Predictive and pharmacodynamics biomarkers are a critical component of today’s process in immuno-oncology drug development.  Join us for this informative webinar to learn about the latest issues in biomarker development and explore the critical junction between pharmaceutical companies, companion diagnostic manufacturers and CROs to enable an effective co-development process.

May 17, 11 a.m. EDT | Register now


Evidence-Based Approaches for Accelerating Patient Enrollment in Oncology

The number of oncology clinical trials has increased exponentially in recent years, putting ever more pressure on increasing clinical trial efficiency by reducing costs and timelines. Discover proven solutions for overcoming the enormous challenge of study planning and patient recruitment from two key experts.

May 24, 11 a.m. EDT | Register now


ON-DEMAND WEBINARS – VIEW NOW

Choosing the Right Fit For Your Functional Provision Service Model

Many sponsors are turning toward a Functional Service Provision Model to lower overhead and enable greater efficiencies. Listen to two of our experts provide key outsourcing strategies in this informative webinar recording. > View webinar now 


The Diabetic Heart: A Focus on Heart Failure 

Hear an insightful discussion on how certain molecular classes impact CV outcomes for patients with type 2 diabetes along with strategies for testing new therapeutic, paradigm-modifying treatment modalities. > View webinar now


Hot Topics in Non-Alcoholic Steatohepatitis (NASH) 

In this webinar, experts discuss:

1) Genetic predisposition and other risk factors for disease progression
2) How to assess and monitor drug-induced liver injury (DILI) in patients.
3) Strategic and statistical considerations for seamless adaptive design in NASH trials.> View webinar now


The Biosimilars Landscape: Key Pieces of the Puzzle for Clinical and Commercial Success: 2017-2021 – What all developers need to know

The regulatory pathway for developing biosimilars in the U.S. is still considered a new frontier. View this webinar as we discuss the key clinical issues sponsors face when navigating today’s regulatory environment. > View webinar now