What criteria is of most value when determining the value of in-house vs. outsourced site payments strategies? Attend this webinar and discover what best practices sponsors and CROs should follow when evaluating a current or future investigator payments partner. Register now!
Where is the medical cost trend headed in 2019? PwC’s Health Research Institute (HRI) annually projects the growth of medical costs in the employer insurance market for the coming year and identifies the leading factors expected to impact the trend. Uncover the factors impacting medical cost trend - from mega-mergers and physician employment trends to healthy advocacy and the increasing customer centricity of healthcare - and what it means for providers, insurers, pharma/life sciences companies and employers. Register now!
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.
Sponsors continually search for opportunities to contain early stage trial costs while addressing increasingly unique study needs and pressure to shorten timelines. Explore how to simplify and streamline Phase I and IIa study execution through clinical technology. Join this webinar and discover how early-stage solutions can give you the competitive edge you need to accelerate your clinical development lifecycle. Register now!
What’s the best strategy to create a holistic syringe-based combination product performance testing program? Start with the fundamentals - ISO and USP considerations. Join West packaging and performance experts as they explain how fit-for-purpose syringe-based combination product packaging involves holistic consideration and testing. 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. Register now.
Discover how evaluating biomarkers in early-phase studies leverages advanced technologies and seamlessly transform millions of data points into actionable insights. This webinar will explore biomarker data trends and challenges, share real-world case studies, and dive into practical technology-based solutions that can be readily implemented. Register now!
How is ICH GCP E6 R2 making it easier for patients to receive the right treatment at the right time? This webinar will explore the essential elements of RBM, straight from the drawing board of ICH E6 R2 working group, and RBM's role in addressing complexities in oncology clinical trials with a roadmap to get ahead. Register now!
There is a remarkable scientific research revolution underway: technology that facilitates highly personalized research workflows is being developed and will soon become mainstream. Far more valuable than simply presenting information, personalized access tools will put the researcher in the driver’s seat, making the best of available content and data by pinpointing to what’s important. Download Now
Each type of tech transfer project presents its own set of challenges. The key to a successful tech transfer is for the vendor and the contract manufacturer to anticipate the challenges and come up with a game plan for the solutions to potential challenges. Challenges can include, timeline of project deliverables (for ANDA or NDA submission), the amount and quality of documentation from develop site, material variances, custom clearances (where applicable), and the added complexity of fast track or orphan designation compounds.
In this webinar, you will hear from manufacturing and engineering experts on:
• The importance of alignment of project management teams from both companies
• Technical transfer & documentation from transfer site to site of transfer site
• Options available to overcome challenges that present themselves during the transfer process
• Equipment lead-time discussions
• Case study including an example of a global tech transfer with fast track approval
To maintain regulatory compliance, life sciences companies must manage the risk associated with storing and moving sensitive content between system layers. See how USDM built a solution on Box to address the issue. Download now.
This webinar will benefit Biotech executives interested in aligning their products for success via early strategy for 505(b)(2) drug development. Register Now
Join Lonza technical and processing experts to learn best practices across complex compounds with a range of solid state, potency, and solubility characteristics. Scale-up considerations will also be discussed and representative case studies presented. Register Now
Learn how cloud-enabled solutions provide real-time insights and actionable analytics to improve clinical trial safety and performance in this short presentation.
The global over-the-counter (OTC) drug market is set to exceed USD $178B by 2024. While expecting lucrative growth, OTC product marketers face increasing competition driven by private label, market consolidation and direct to consumer brands.
This webinar will review global OTC market trends and drivers, consumer trends, present case studies on the impact of introducing new forms, and provide information on innovative and consumer-preferred dose forms to help you grow your OTC brand. Register here!
There are many parenteral dosage forms from which the pharmaceutical scientist can choose to develop their drug product. In this article, the author discusses the choices available and strategies which can be employed at the different stages of development.