This webinar will address challenges encountered when leveraging Real-World Evidence such as finding the “right” data set, identifying high priority use cases to show quick wins, and creating integrated evidence plans across a product’s lifecycle. Register Now!
The number of pediatric drug approvals has increased 5 fold over the last 20 years, rising from 10-20 approvals per year to 50-60 annually today. Increased awareness around pediatric medicine and FDA support for pediatric clinical research are just some of the factors contributing to this growing market. Register Now!
In this webinar you will hear from industry experts on:
- How to manage stability challenges for accelerated approval programs
- Fit-for-purpose manufacturing strategies
- Overcoming scale-up challenges
- Developing a comprehensive solution for unexpected challenges
- Avoiding typical pitfalls in accelerated programs
Traditional-based learning within life sciences is still considered the norm, yet this type of training is limiting. Sales reps, marketing liaisons, and clinical trainers need to move away from the archaic way of distributing information in order to improve engagement, both internally and externally. Register Now!
This webinar will discuss development considerations for CBD and other cannabis-derived products from a clinical, preclinical (pharmacology/toxicology), CMC, and regulatory perspective. Register now.
During this webinar, PwC’s Health Research Institute will review findings from a new global survey of industry executives, and provide analysis and commentary on key drug pricing issues. Register Now!
Selecting a device partner for combination product development should be based on several key considerations. This webinar will provide insights into the elements that guide the selection of a device partner, including a proposed approach that consists of a quantitative assessment of risks and benefits.
The market for orally disintegrating tablets (ODT) has grown annually and is projected to reach US$21B in 2023. Attend this complimentary webinar on patient-centric drug development and advanced ODT technologies in Japan and the US. Register now!
Join this webinar to discover the advantages of using Signatera™ (RUO), a novel assay custom-designed for each patient that detects circulating tumor DNA (ctDNA) with high sensitivity and specificity to monitor molecular residual disease, early recurrence, and treatment response across solid tumors. Register Now!
In this webinar, you’ll learn how to use static analysis to ensure continuous compliance with industry standards and regulatory requirements, improve security for increasingly connected medical devices, and enforce corporate and industry coding rules and best practices. Register Now!
In this webinar, we will review the current OTC remedies for cough, cold and allergy categories and discuss strategies to grow your share on shelf space with innovative dosage forms.
Technology is impacting every aspect of our lives, and the life sciences industry is no different—it is changing the way companies operate. The need to embrace change is an imperative for these companies to stay competitive and continue to deliver on patient needs. Register Now!
To achieve adaptable and scalable trial execution, a mindset change and more flexible approach to data management is necessary. Join this webinar to hear industry experts discuss three key lessons learned when applying Agile Development Methodology principles into your work in data management.
Join Dr. David Gosalvez to see how R&D productivity can be improved in three critical areas: Lead Discovery, Screening and data capture. Register Now!
Serialization is a great achievement for our industry. However, most executives now realize that it is only part of the solution and serialization alone cannot solve the escalating problems of counterfeiting and diversion within the Pharmaceutical industry.
In this webinar we will discuss going beyond serialization and understanding why it’s not enough and the need to stay innovative and add value and protection to your current solutions. Register now.
Join as Diane Hayes, PHD, InCrowd President and Co-founder, reviews the results from the 2019 physician predictions survey and considers the year ahead. Register Now
This webinar will benefit executives at Biotech and Pharmaceutical companies interested in learning more about 505(b)(2), the pathway of choice. When executed properly, this regulatory pathway enables a lower cost, lower risk, and faster path to approval and market. Register Now!
Navigating patient-reported outcomes (PROs) such as unobservable symptoms, treatment satisfaction, quality of life, and treatment adherence is a critical component of a patient centric healthcare system. Join our experts in the first of a three-part webinar series on PROs, as they provide insight on the foundational elements of PROs and recent regulatory trends. Register now!
Hear new results from one of the industry's largest, global clinical operations surveys, the Veeva 2018 Unified Clinical Operations Survey. The Veeva 2018 Unified Clinical Operations Survey examines the industry’s progress toward a unified clinical operating environment.
Researchers are encumbered with a plethora of disparate data and analytic tools. These assets pose several challenges which need to be overcome to ensure they satisfy their intended purpose.
Join this webinar to learn how real-time, self-service access to longitudinal patient data is changing the way researchers evaluate treatment effectiveness, safety, protocol design, and more. Register now.
Fraud and fabrication is no laughing matter in the realm of clinical trials.
This webinar will outline the ways in which sponsors and CROs can remain diligent by being aware of signs of possible fraud and fabricated data throughout the course of the study.