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All Upcoming Webinars

  Date Webinar Title Synopsis

Aug 24, 2017 Medical Devices: Reviewing Regulatory Changes in the US and EU LifeScience -  This webinar will discuss steps to ensure regulatory compliance and an uninterrupted supply of medical devices in the marketplace, and share insight and best practices from experience in navigating US and global regulations on medical device development
Speakers: Angela Stokes, Senior Director, Regulatory Consulting, INC Research/inVentiv Health
Eric Distad, Executive Director, Clinical Development, Medical Device and Diagnostics, INC Research/inVentiv Health

Aug 29, 2017 Moving Beyond Regulatory and Performance Metrics in Starting Clinical Trials LifeScience -  Topics include a discussion on business intelligence derived from clinical trial data and industry trends on data mining and analytics
Speakers: Barry Milton, Head of Business Operations, Novartis
Jeffrey Kasher, President, Patients Can't Wait
Rob Wynden, VP Technology & Engineering, goBalto

Aug 29, 2017 Planning and Conducting Trials of the Latest Immunotherapies LifeScience - In this webinar, the speakers discuss the factors that sponsors must take into account as they design and execute clinical trials in this space, beginning with a review of the immunotherapy landscape
Speakers: Joseph O’Connell, MD, Vice President, Medical & Scientific Affairs, Hematology & Oncology, INC Research/inVentiv Health
Tony Catka, PhD, Senior Director, Regulatory Policy & Intelligence, INC Research/inVentiv Health
Len Correale, JD, Associate Director, Feasibility Optimization & Site Intelligence, INC Research/inVentiv Health

Aug 31, 2017 Outsourcing Analytical Testing for Biologics from a CRO Point of View LifeScience - This webinar will provide the audience with a general explanation of how CROs can support biologics testing, ranging from product release and stability to in-depth structural elucidation and degradation pathway studies
Speaker: Min Zhao, Ph.D., Director, Analytical Services for Biologic Product - CMC Services, Frontage Laboratories, Inc.

Aug 31, 2017 ISO 13485:2016 for Medical Device Manufacturers: Ensuring a Smooth Transition through Effective Preparation LifeScience - This webinar will discuss the steps that medical device manufacturers should take now to effectively prepare for the new standard by the mandatory implementation date in 2019
Speaker: Linda Mummah Schendel, Principal Medical Research Manager, NAMSA

Sep 6, 2017 Why Making Every Product Truly Unique is the Key to Modern Brand Protection LifeScience -  In this session, you will learn about Systech’s ability to create trusted uniqueness in every product, and how this idea is central to a modern approach to brand protection
Speaker: Jim Sinisgalli, Director of Product Management and Brand Protection, Systech

Sep 7, 2017 Solvents, Polymers & Cyclones – Bioavailability Enhancement through Spray Dried Dispersions LifeScience - Discussions will include spray dried dispersion formulation development and early phase considerations for finished dose development
Speaker: Stephie Lee, Associate Scientist, Catalent
Eric Gorman, Research Scientist II, Gilead Sciences

Sep 8, 2017 Overcome Pharma Data Challenges to Improve Outcomes and Operations: Lessons Learned from Other Industries LifeScience -  Learn what the future holds for the healthcare and pharma ecosystems making the digital transformation, leveraging big data – including new and existing data sources – and using technologies to enhance clinical and operations processes
Speaker: Gary Palgon, Vice President, Healthcare and Life Sciences Solutions, Liaison Technologies

Sep 12, 2017 The Role of Clinical Endpoint Committees in Medical Device Trials LifeScience - This webinar will discuss the value of clinical endpoint committees in medical device evaluation programs and explore the process of organizing, managing, and implementing a centralized adjudication process for standardizing study endpoints
Speaker: Joanne Emmett, Vice President, Medical Device & Diagnostics, Premier Research
Janet Kube, Director, Project Management, Premier Research

Sep 13, 2017 Striking While the Iron is Hot: Pharmaceutical Cocrystals as Drug Substance
The Latest FDA Guidance and Regulatory Implication
LifeScience -  Learn innovative patent strategies for cocrystals, how solid form claims are drafted, and examples of recent case law
Dr. Steef Boerrigter, Sr. Research Scientist, AMRI
Eyal Barash, JD

Sep 13, 2017 IRT Best Practices: How Companies are Accelerating Timelines While Improving Quality

LifeScience - This webinar will highlight the use of more innovative agile methodologies to achieve better project delivery predictability, streamlined processes and high quality studies
Amanda Nite, Senior Director, RTSM Operations and Commercial Solutions, Bioclinica
Robin Barber, Manager, RTSM Solutions Engineering, Bioclinica

Sep 13, 2017 Optimize the Imaging in Clinical Trials by Aligning Operational Excellence and Scientific Expertise LifeScience - This webinar will discuss real-world scientific and operational examples of errors that can occur during your imaging clinical trial, and address how you can anticipate, but most of all avoid them
Speakers: Edward Ashton, Ph.D., Vice President, Oncology Imaging, BioTelemetry Research (Cardiocore & VirtualScopics)
Danielle Lewis, M.S., PMP, Global Operations Account Manager, BioTelemetry Research (Cardiocore & VirtualScopics)

Sep 13, 2017 Are Humidity Fluctuations Compromising Your Capsule Quality? LifeScience - The speaker will demonstrate how pharmaceutical manufacturers can benefit from desiccant dehumidification solutions regardless of the local climatic conditions
Martin Ginty, Industry Manager, Pharmaceutical, Munters GmbH

Sep 14, 2017 Advancing Bioabsorbable Scaffolds with Polymer Technology MedicalDevice - Bioabsorbable vascular scaffolds (BRS) have been clinically shown to afford restored vasomotion, late luminal enlargement, and reduced angina; all benefits of a new vascular restoration therapy that is expected to improve the life of many patients
Speakers: Dr. Bruce Anneaux, Ph.D., Corporate Director, Research, Zeus
James M. Lindsey, III, Sr. Research Engineer, Zeus

Sep 15, 2017 Build a Strong Food Safety Culture from the Top Down FoodSafety - This webinar will review key considerations within food safety, procurement, merchandising, operations and training/human resources, at the director/manager level, offering techniques to influence the right choices and building culture, therefore helping to manage the change associated with gaining commitment and follow through
Speakers: Ken Leith, co-author, Food Safety, A Roadmap to Success
Patti Leith, co-author, Food Safety, A Roadmap to Success

Sep 18, 2017 How Innovations in Data Visualization Are Accelerating Data Cleaning and Improving Quality

LifeScience -  Topics for this webinar include applying insights to focus data cleaning efforts, methods of tracking the activities needed to achieve DB lock, eEarly warning systems that help you avoid delays, and mMethods of ensuring no data has changed since
Karen McPoyle, Director, Data Strategy & Solutions, Bioclinica

Sep 19, 2017 Agile IRT/RTSM: Enabling Clinical Trial Design and Supply Innovation LifeScience - This webinar demystifies the term "agile," from an operational perspective, while highlighting the speed and flexibility these systems offer to be able to support complex protocols that require accelerated changes
Speaker: Kathleen Greenough, Client Services Lead, 4G Clinical

Sep 19, 2017 Chronic Pain: Conducting Clinical Trials in Osteoarthritis LifeScience - In this webinar, the speakers will examine  Osteoarthritis as a flexible model for development of new therapies, the design of clinical trial protocols to address the special needs of the drug being studied, and more
Speakers: Michael Kuss, Vice President, Strategic Development, Analgesia, Premier Research
Scott Millard, Executive Director, Strategic Development, Analgesia, Premier Research

Sep 20, 2017 CRO Benchmark Survey: CROs’ Perspective of Oversight and Collaboration LifeScience -  This webinar will present findings from a new benchmark survey conducted across leading CRO executives and project team members, to shed light on the challenges associated with managing increasing complexity of data, maintaining milestones at greater economy, and addressing new requirements from guidance such as ICH E6(R2)
Speaker: Julie Peacock, Client Services, Comprehend

Sep 21, 2017 Reducing Clinical Trial Failure With New Tools for Drug Target Identification and Prioritization LifeScience - Combining the right tools and workflows with the right data will lead to better decisions and more drugs to alleviate suffering
Speakers from Clarivate Analytics:
Dr. Richard K. Harrison, Chief Scientific Officer
Aleksey Dubovenko, Discovery Sciences Product Manager
Matt Wampole, Manager, Solution Scientist Team

Sep 21, 2017 Tactics for Successful Patient Recruitment in Alzheimer's Clinical Studies LifeScience - In this webinar, the speaker will consider strategies for timely patient recruitment and retention for Alzheimer's clinical trials and discuss guidelines for, and technologies to support patient recruitment
Speaker: William A Holt, DO, Executive Director, Scientific Affairs, Neurosciences, PRA Health Sciences

Sep 22, 2017 Outcomes-Based Agreements and Innovative Contracting for Biopharmaceuticals: Where Is The Market Moving? LifeScience - 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: Guy Sherwin, Lead Consultant, EU Pricing and Market Access, Commercialisation and Outcomes, ICON

Sep 22, 2017 Innovation through Integration – Providing Next Generation Biomedical Devices and Interconnects

LifeScience - Topics in this presentation include the key biomedical packaging technologies, the elements of innovation and integration in new biomedical packages and interconnects,and how miniaturization principles can be implemented in biomedical packaging
Speaker: Steve Groothuis, Chief Technology Officer, Samtec Microelectronics

Sep 26, 2017 Clinical Payments Case Studies: Improving Efficiency, Cash Management, and Compliance

LifeScience - The presentation will include case studies of how trial sponsors and CROs are automating the clinical payments process to improve accuracy and operational efficiency, while gaining greater control over cash management
Speaker: Lorie McClain, VP, Product Management, Product Development & Technology Bioclinica, Inc.

Sep 27, 2017 Lugano 2014 Criteria for Assessing FDG-PET/CT in Lymphoma: An Operational Approach for Clinical Trials

LifeScience - This webinar will discuss the evolution of the role of imaging in the assessment of lymphomatous disease, with a focus on the recently implemented Lugano criteria
Ronald Van Heertum, MD, Vice President, Medical Affairs, Oncologic and Molecular Imaging, Bioclinica
Robert Scarimbolo, Director, Medical Affairs, Oncologic and Molecular Imaging, Bioclinica
Zachary LaVoie, Manager, Medical Affairs, Oncologic and Molecular Imaging, Bioclinica

Sep 28, 2017 Development and Manufacture of Highly Potent API Drug Products Throughout the Clinical Phases LifeScience - The speaker will share how highly potent APIs can be developed and manufactured into suitable drug products that meet the quality target profiles
Speaker: David O’Connell, Director Pharmaceutical Development, PCI Pharma Services

Oct 3, 2017 What Does it Take to Successfully Execute Large, Global, Phase III Programs? LifeScience - What does it take to successfully execute a program of this nature? The speakers will break down some of the best practices and crucial elements for executing programs in this challenging environment
Speakers: Clifford McIntosh, Vice President, Strategic Alliance Management, INC Research/inVentiv Health
Alexandria Wise-Rankovic, Ph.D., Senior Vice President, Clinical Development, CNS, INC Research, inVentiv Health

Oct 4, 2017 Pharmacology to Payer: One Quantitative Drug Development Framework to Rule Them All LifeScience - Viewers will learn why P2P offers an unprecedented opportunity to create impactful solutions that will help address market failures in drug development
Speakers: Craig Rayner, President of Consulting Services, Certara
Carl Kirkpatrick, Professor of Pharmacy and Pharmaceutical Sciences, Monash University

Oct 4, 2017 Biologics in Dermatology: Considerations for Patients and Clinical Trials

LifeScience - This webinar explores the evolution of biologics within the dermatology landscape, with an emphasis on clinical trial considerations for sponsors developing biologic agents
Speakers: Darcee Duke Strube, Senior Vice President, Dermatology Division, Novella Clinical
Dr. James J. Milbauer MD, Dermatologist, Medical Monitor, Advisor

Oct 5, 2017 Strategy Design & Formulation Considerations for GLP Toxicology Studies LifeScience - This session will discuss how to prepare for a GLP toxicology study, including evaluating critical areas in the drug development process to help ensure a successful toxicology study
Speakers: Grace M. Furman, PhD, DABT, CEO and President, Paracelsus, Inc.
Meredith Perry, Senior Scientist, Catalent

Oct 5, 2017 NextGen Data Mapping Solutions for Better, Faster Compliance and Analytics LifeScience -  Hear how new solutions leveraging proven technologies can help expedite and automate this complex process – providing significant time and cost savings while ensuring data quality for your submissions
Speaker: Dave Stein, President & Owner, D. Bartley Consulting

Oct 26, 2017 Pharmacovigilance Database E2B(R3) Compliance: A Technical and Practical Perspective LifeScience - This webinar is suitable for both those looking for an introduction to the updated pharmacovigilance standards and those looking to ensure they can implement the necessary changes within their department or team
Speakers: Tom Nichols, Senior Director, Pharmacovigilance, Quanticate
Dr. Marc Zittartz, Chief Quality Officer, pharmasol

Nov 7, 2017 Preparing for Phase II: Finding the Right Dose, Schedule, and Combination from your Phase I/II Oncology Clinical Trial LifeScience - This webinar will review these and other factors important to planning and executing early-phase oncology clinical trials in preparation for a decision-making Phase II trial
Speakers: Paul Hallenbeck, Ph.D., Executive Director, Strategic Development, Oncology, Premier Research
Peter Larson, M.D., Senior Medical Director, Hematology-Oncology, Premier Research
Gabriele Accetta, Principal Biostatistician, Premier Research

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