Best Practices to Meet Financial Objectives When Selecting an Investigator Payments Partner
Recorded on: May 16, 2018 | 1pm ET / 10am PT | Bioclinica

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!

PwC Health Research Institute's Medical Cost Trend: Behind the Numbers 2019
Tuesday, June 26, 2018 | 11am ET / 8am PT | PwC

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!

The Changing Landscape of Real-World Evidence and its Impact on Clinical Research
Thursday, June 21, 2018 | 11am ET / 8am PT | TriNetX

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.

Fast Track your Early Clinical Development Lifecycle
Wednesday, June 20, 2018 | 11am ET / 8am PT | Medidata Solutions

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!

Demystifying Performance Testing: Strategies to Qualify Combination Products
June 18, 2018 | 11am / 8am PT | West Pharmaceutical Services, Inc.

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!

Handling Suspected Fraud and Data Fabrication in Clinical Studies
Wednesday, June 13, 2018 | 1pm ET / 10am PT | Rho


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.

Overcome Data Chaos with QuartzBio: Turn Biomarker Data Sets into Actionable Insights
May 29, 2018 | 2pm ET / 11am PT | Precision for Medicine

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!

RBM: The Missing Link Bringing Drugs to Market Efficiently
May 23, 2018 | 11am ET / 8am PT | Medidata Solutions

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!

Putting The Researcher In The Driver’s Seat: The Race To Connecting Workflow Tools in Life Sciences Research
Reprints Desk

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

Overcoming Technology Transfer Challenges
May 17, 2018 | 11am ET / 8am PT | Catalent

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 

Learn more, and register, here!

[Cloud assurance kit] GxP Validation in the cloud with Box & USDM

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.

505(b)(2) Strategy for Biotech Execs: Positioning Your Products for Success
May 9, 2018 | 11am ET / 8am PT | Camargo

This webinar will benefit Biotech executives interested in aligning their products for success via early strategy for 505(b)(2) drug development. Register Now

Pushing the Boundaries of Micronization in Drug Delivery
May 3, 2018 | 11am ET / 8am PT | Lonza

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

A Simpler Approach to RBM in Clinical Trial Management
Veeva Systems at 2018 SCOPE Summit

Learn how cloud-enabled solutions provide real-time insights and actionable analytics to improve clinical trial safety and performance in this short presentation.

Improving Your Fair Share: Expanding your OTC Brand with a Consumer Preferred Dose Form
Recorded on April 26, 2018 | Catalent

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!

Whitepaper | Choosing the Best Steriles Dosage Form for Your Phase I Clinical Supply Needs

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. 

Five Tracking Spreadsheets it’s Time for Regulatory to Retire
Veeva Systems

Find out how to eliminate regulatory’s tracking spreadsheets for good. Read more