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Upcoming Life Science Webinars

  Date Webinar Title Synopsis

May 25, 2017 Thermal Processing Systems for the Food Industry: A Guide to Selecting Thermal Equipment and Technology Food Manufacturing -  Speakers will review the criteria used to select the best thermal technology solutions for real-world applications
Speakers: John Heapy, Application Engineer Thermal Products, Bepex International LLC, Scott Halvorsen, Director of Thermal Technology, Bepex International LLC

May 25, 2017 EU IVD Regulation: Top Five Changes for Medical Device Manufacturers to Consider LifeSciences -  This webinar will help viewers better understand the significant changes that IVD manufacturers should prepare for now in order to be successful under the new regulation
Speaker: Valynda Machen, CQA, RAC, Principal Medical Research Manager, Regulatory, NAMSA

Jun 1, 2017 Rare Disease & Orphan Drug Development: Cost-Efficient Trial Design to Minimize Cash Burn LifeSciences - Topics include key challenges to improve cost-efficiency in orphan drugs clinical development, regulatory evolution in the review process of Orphan Drugs, and what role multi-stakeholder collaboration in rare disease research plays in improving clinical trials cost-efficiency
Speakers: Carlos R. Camozzi, MD, Chief Medical Officer, Simbec-Orion Group
Fabrice Chartier, PhD, Chief Operating Officer, Simbec-Orion Group

Jun 5, 2017 eTMF Workflows: Active eTMF to Improve the Quality of Clinical Trials LifeSciences - This webinar will cover various aspects of proper organisation of eTMF workflow
Speakers: Dmitriy Gorichev, CEO, ClinDisc s.r.o.

Jun 5, 2017 Choosing the Right Partner to Build a Successful Direct-to-Patient (DTP) Clinical Trial Framework LifeSciences -  Topics include how DTP trials can contribute to the improvement of patient enrollment, retention and overall patient satisfaction, what to look for in a partner to manufacture, package and distribute clinical drug supplies for DTP studies, protocol requirements for DTP trials, and pharmacy licensing regulations and how they impact distribution
Speakers: Mia Kobuta, Manager, Logistics Client Services, Sharp Clinical Services Inc.
Will Plyler, Manager, Business Development – Clinical Research Services, McKesson Specialty Pharmacy Solutions

Jun 6, 2017 5 Qualities to Consider When Selecting Clinical Pharmacology Units for Early Drug Development LifeSciences - Coming from a both a CRO and clinical pharmacology unit perspective, WCCT Global offers insight into the five qualities that are most indicative of a high-performing, optimized Phase 1 clinical pharmacology unit
Speaker: Jon Rojas, CEO, WCCT Global

Jun 7, 2017 Using Early Economic Models in Developing your Evidence Strategy LifeSciences - Join us to learn best practices for developing early economic models to inform key strategic decisions
Speakers: Victoria Paly, MHS, Senior Health Economist, ICON
Dhvani Shah, MS, Lead Health Economist, ICON

Jun 8, 2017 The Good, the Bad, the Necessary in Rare Disease Studies LifeSciences - This webinar will discuss the why, where, when and how a rare disease drug is intended to be used subsequent to approval and the importance of beginning with the end in mind
Speakers: Cinzia Dorigo, PharmD, Executive Director, Clinical Development, INC Research
Alastair MacDonald, Executive Director, Real World & Late Phase, INC Research
Heather Medlin, Executive Director, Real World & Late Phase, INC Research

Jun 8, 2017 How to Upgrade Kombucha and Functional Beverage, Food, Supplement Products with Symbiotic Botanical Fermentation Food Manufacturing - Discover the next market opportunities in kombucha and botanicals
Speaker: Chantale Houle, President, Kefiplant

Jun 8, 2017 Self-Administration Injection Systems – A Change in Market Trends Requires a Rethinking of Your Compounds Packaging LifeScience - This webinar will provide insight on the advantages of prefilled syringes and cartridges, including the various differentiators of the most commonly used syringe platforms – presterilized and bulk. Issues such as customization in packaging materials and production steps, challenges for dealing with complex compounds such as silicone sensitivity, reduced particle load and more are reviewed and solutions discussed.
Speaker: Kevin Joseph Wrigley, Product & Service Manager, Vetter Pharma International GmbH

Jun 12, 2017 Uncover Pharmacovigilance Insights with Data Discovery and Active Surveillance LifeSciences - See how drug safety teams can use dynamic visual analytics to uncover safety issues earlier
Speakers: Masha Hoffey, Director of Clinical Analytics, PerkinElmer Informatics
James (Jamie) Powers, Director of Real World Evidence and Data Science, PerkinElmer Informatics

Jun 12, 2017 Pharmaceutical Case Studies Illustrating Data Analytics Strategies
Extracting the Most Value from Your Data Assets
LifeSciences - This webinar will focus on specific pharmaceutical case study examples, with a focus on the Seeq software application
Speakers: Lisa J. Graham, Ph.D., P.E., CEO and Founder, Alkemy Innovation Inc.
Brian Crandall, Analytics Engineer, Seeq

Jun 13, 2017 Complex Generics: Physicochemical Characterization Analysis for Deformulation and In Vitro Bioequivalence Studies LifeScience - This webinar will appeal to scientists involved in the development of generic drugs, particularly those considered complex generics because of their formulation or method of delivery
Speakers from Malvern Instruments:
Dr. Paul Kippax, Director of Product Management - Morphology
Dr. Anne Virden, Technical Support Supervisor - Analytical Imaging and Laser Diffraction
Dr. Katy Langley, Associate Product Manager - Analytical Imaging

Jun 14, 2017 Pharmacovigilance Oversight – Best Practices for Safety IT LifeScience - Find out how the use of information technology for drug safety has evolved over the last decade in line with changing demands from the business
Speakers Andrew Mitchell, Director of Life Sciences, Synchronoss
Kapil Kedia, Founder & CEO, SyNRG Solutions Technologies

Jun 15, 2017 The Evolving Utilization of Specific Biomarker Roles Within Trial Design LifeScience - This webinar will examine the use of targeted clinical strategies are as a critical step towards improving success rates
Speakers: Dr. Richard K. Harrison, Chief Scientific Officer, Clarivate Analytics
Gavin Coney, Head of Clinical Products, Clarivate Analytics

Jun 15, 2017 Tumor-Size-Based Measurements as Endpoints in Cancer Clinical Trials LifeScience - This webinar will provide an overview of the use of endpoints based on tumor measurements in cancer clinical trials
Speakers: Tomasz Burzykowski, PhD, VP Research, International Drug Development Institute (IDDI)
Everardo Saad, MD, Medical Director, International Drug Development Institute (IDDI)

Jun 20, 2017 Medicinal Chemistry Excellence – Efficient and Innovative Solutions for Superior Preclinical Candidates LifeScience - During this webinar, the speaker will describe Evotec’s medicinal chemistry and drug discovery philosophy
Speaker: Dr. Craig Johnstone, EVP, Global Head of Chemistry and Directeur General, Evotec France

Jun 21, 2017 Quantitative Protein Profiling in FFPE to Characterize Toxicities Associated with Immune Checkpoint Inhibitors LifeScience - Immune checkpoint inhibitors (including anti-CTLA-4 and anti-PD-1) have shown substantial clinical success in many cancers but have been linked to rare immune-related adverse events (irSAE)
Speakers: Joseph M. Beechem, PhD, Senior VP of Research & Development, NanoString Technologies
Justin Balko, PharmD, PhD,, Assistant Professor of Medicine and Cancer Biology, Vanderbilt University Medical Center

Jun 21, 2017 Serialized? Yes. But are Products Still Being Diverted? LifeScience - Pharmaceutical manufacturers are scrambling to meet Serialization deadlines, most notably in the USA and EU, and many have already. But even when you serialize, the reality of product diversion still exists. How can we leverage your serialization investment to combat ever-increasing product diversion?
Speaker: Joe Lipari, Director of Cloud Products, Systech International

Jun 22, 2017 Are You Choosing the Right Model? A Guide to Selecting Your Next Immuno-Oncology Model LifeScience - Viewers will learn about the latest in vivo cancer pharmacology models, what to consider when choosing the proper model, and how these models are used to investigate combination regimens of multiple immuno-therapies and immunotherapeutics combined with other treatment modalities, which correspond to current clinical investigations
Speaker: Dr. Michelle Mack, Global Director, Scientific Engagement, Crown Bioscience Inc.

Jun 26, 2017 Imaging-based Subtypes of Pancreatic Cancer LifeScience - Definiens has developed quantitative methods to analyze the CT images and diagnostic pathology of patients, associating these measurements with outcomes
Speaker: Eugene J. Koay, MD, PhD, Assistant Professor, Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center

Jun 27, 2017 How Improving Site Payments Can Make You the Sponsor/CRO of Choice LifeScience - Viewers will learn how sponsors and CROs that implement clinical payments solutions are benefiting from increased control over study cashflow, improved operational efficiencies, and better compliance
Speaker: Lorie McClain, VP, Product Management, Product Development & Technology, Bioclinica, Inc.

Jun 28, 2017 What Can Real-time Insights and Analytics Achieve for Your Clinical Trials? LifeScience - In this webinar, speakers will demonstrate live the power of real-time clinical data insights and analytics, and what this means for clinical trial conduct and for clinical trial management activities
Speakers: Stephanie Langouet, Vice President, Data & Analytics, Cmed
Jon Carter, Product Manager, Cmed

Jun 28, 2017 Best Practices for CRO Oversight: How an Oversight Capability Maturity Model and Automation Drive Speed and Quality of Clinical Trials LifeScience -  For this webinar, Comprehend has partnered with Avoca to share industry best practice for oversight blended with their best in class clinical intelligence applications
Speakers: Julie Peacock, Client Services, Comprehend
Janis Hall, Senior Consultant, The Avoca Group

Jun 29, 2017 Pharmaceutical Serialization – Best Practices for Global Commercial Supply in an Evolving Market LifeScience - The speaker will share his experiences in developing PCI’s serialization technology platform, along with developing and executing PCI’s strategy for supplying commercial serialized products to domestic and emerging markets across the globe
Speaker: Ian Parsonage, Senior Director, Global Serialization Services (Global Engineering), PCI Pharma Services

Jul 10, 2017 Digital Transformation in the Clinical Trial Process: Increasing Patient Enrollment and Patient Data Exchange LifeSciences - Join the speakers to discover ways to leverage the digital transformation in pharma to stimulate greater and faster recruitment as well as improve patient and research data harmonization and exchange
Speakers: Bethany Bray, CEO and Founder, AutoCruitment
Gary Palgon, Vice President, Healthcare and Life Sciences Solutions, Liaison Technologies

Jul 11, 2017 Integrating Equipment Design, Logistics Processes and Real-Time Informatics: The Arrival of QbD in Pharmaceutical Logistics LifeSciences - This webinar will discuss the Quality by Design process as it relates to logistics and evaluate its benefits
Speaker: Mark W. Sawicki, Ph.D., Chief Commercial Officer, Cryoport

Jul 26, 2017 Using Model Reduction to Bridge the Quality Systems Pharmacology-Pharmacometrics Divide LifeSciences -  In this webinar, Dr. Tom Snowden will demonstrate why model reduction methods are a potent and necessary tool in the modeler’s arsenal, can be applied to QSP models, and used to extract scientific and business insights from complex models
Speaker: Tom Snowden, Research Scientist, Certara

Sept 22, 2017 Outcomes-Based Agreements and Innovative Contracting for Biopharmaceuticals: Where Is The Market Moving? LifeSciences - Viewers will get a deeper understanding of the changing contracting landscape and to learn ways to leverage new and innovative approaches to improve the commercial success of your biopharmaceutical products
Speaker: Janice Watch, Divisional Principal, Head of EU Pricing and Market Access, ICON Commercialisation and Outcomes

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