Upcoming Webinars Archived Webinars Training Vitals Host A Webinar About Get Updates Contact

All Upcoming Webinars

  Date Webinar Title Synopsis

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
Speakers:
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 of Scientific Affairs, 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 4, 2017 Why Track and Trace Isn’t Just Tracking and Tracing: Best Practices for Implementing a Solution That Works LifeScience - This webinar will discuss a holistic approach towards designing and achieving a successful Track and Trace solution
Speaker: Joe Lipari, Director of Cloud Products, Systech International

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
Sam Anwar, Vice President, Engineering eClinical Solutions

Oct 10, 2017 Pharma Competitive Intelligence: Delivering Actionable Insights for Decision Making LifeScience - This webinar will provide insight into current pharma competitive intelligenceI, including trends and best practices
Speakers: Jamie Munro, Global Practice Leader, Portfolio and Licensing, Clarivate Analytics
Karthik Subramanian, Senior Product Strategy Manager, Clarivate Analytics

Oct 10, 2017 Electronic Informed Consent: 2017 Industry Survey Results from Clinical Sites LifeScience - During this webinar, the speakers will reveal the results of CRF Health’s “Electronic Informed Consent: 2017 Industry Survey Results - Site Edition.” This site-specific survey gathered feedback from 105 respondents in roles including study coordinator, clinical research associate (CRA), investigator, and researcher
Speakers: Sam Sather, Quality and Regulatory, TrialConsent, CRF Health
Giga Smith, Director of Research, Coastal Carolina Health Care

Oct 11, 2017 Beware the Hidden Costs of Conducting Clinical Trials: Understanding the Landmines and How to Avoid Them LifeScience - In this webinar, the speakers will explore four areas that can dramatically increase the cost of your clinical program and offer insight into elimination and control of hidden costs through the use of a cardiovascular-based case study
Speakers: Deborah Schmalz, BS, Executive Director, Executive Director, Medical Device, Medpace
Courtney Busemeyer, Med, Senior Director, Data Management, Medpace
Celeste A. Morris, PhD, RAC, Medical Writer, Regulatory Affairs, Medpace

Oct 11, 2017 Claims Substantiation – An Integrated Clinical and Regulatory Approach FoodManufacturing -  With a strong, proven claim, companies can differentiate their brand while reinforcing the product’s health and nutritional benefits and performance
Speakers: Josh Baisley, B.Sc., Director of Clinical Trials, Nutrasource
Will Rowe, B.A., President, CEO and Co-Founder, Nutrasource
Rachel Rebry, M.Sc., Associate Director, Regulatory Affairs, Nutrasource

Oct 11, 2017 Overcoming the Challenges of Conducting Clinical Studies in Rare Pediatric Populations LifeScience - In this webinar, the speakers will highlight some of the key challenges associated with conducting research within rare pediatric populations that are few in number to begin with, are geographically dispersed and are often not located near a research center
Speakers: Scott Schliebner, Vice President, Rare Disease - Scientific Affairs, PRA Health Sciences
Mark Sorrentino, MD, Vice President, Center for Pediatric Clinical Development, PRA Health Sciences

Oct 12, 2017 Food Safety: How Representative Sampling Can Reduce Your Risk FoodSafety - Attendees of this webinar will learn how a representative sampling plan improves assessment of the characteristics of the entire lot, batch, or process stream to avoid food hazards
Speaker: John Powalisz, Industry Manager, Sentry Equipment

Oct 13, 2017 Linking Evidence and Value Strategies with the Right Stakeholder LifeScience - Join the speakers as they discuss an approach to evidence-generation strategies in drug and medical device development that enables integrated teams to develop and implement targeted and effective value propositions
Speakers:
Paul Just, PharmD, Senior Principal, Medical Device Health Economics, Commercialisation & Outcomes, ICON
Sarah Clifford, PhD, Senior Principal, Clinical Outcomes Assessments, Commercialisation & Outcomes, ICON

Oct 13, 2017 Adaptive Trial Design and Incorporation of Biomarkers to Maximize Achievable Objectives in Early Phase Clinical Studies LifeScience - This webinar will discuss adaptive designs and focus on strategies for achieving additional objectives through the inclusion of biomarker evaluation in Phase 1/2 clinical trial design
Speakers: David R. McIlwain, PhD, Scientific and Medical Affairs Subject Matter Expert, WCCT Global
Kalyan Ghosh, Vice President, Biostatistics, WCCT Global

Oct 16, 2017 Cardiovascular Safety in Biopharmaceutical Product Development – From QT Prolongation and Beyond

LifeScience -  Objectives for this webinar include providig a background and perspective on the use of QT prolongation as a cardiac safety endpoint within drug development, and taking it forward to the more recent discussions beyond the Through QT (TQT), learning about additional ECG intervals under discussion related to cardiac safety assessment, plus an overview of the discussion around the use of long term ECG capture versus the 10 second ECG signal/waveform in clinical trials
Speakers:
Jeff Heilbraun, MS, VP Strategic Development, Cardiovascular Safety Services, Bioclinica
Bruce Lloyd, MD, Associate Medical Director and Director of Clinical Cardiology Services, Bioclinica

Oct 16, 2017 Navigating Clinical Supply Challenges in Emerging Regions LifeScience - Having a thorough understanding of a country’s regulatory requirements includes understanding both the written and unwritten regional differences and business practices
Speaker: Rognvald Lamb, Global Transportation Manager, Catalent Pharma Solutions

Oct 17, 2017 Daily Diabetes Management in the Virtual World LifeScience - In this webinar, the speakers will be discuss how they used a Design Thinking Methodology approach for insight and prototype generation
Speakers: Kevin Duvall, Sr. Manager, Patient Engagement Strategy, Sanofi Pasteur
Patricia Roselle, Global Head, Patient Network Management, Sanofi Pasteur
Brad Pruitt, M.D., MBA, Executive Director, Chief Medical Officer, PRA Health Sciences

Oct 18, 2017 Vendor Oversight: Five Best Practices in Optimizing Limited Resources LifeScience -  This webinar will present the challenges and opportunities sponsors face when managing with limited resources, providing best practices based on a real-world case study of how a sponsor was able to increase trials and optimize their CRO relationship
Speakers: Julie Peacock, Client Services, Comprehend
Laurie Halloran, Founder, Halloran Consulting Group

Oct 18, 2017 Pediatric Best Practices for Recruitment and Retention in Clinical Trials LifeScience - In this webinar, the speakers will cover best practices for recruitment and retention for pediatric studies
Speakers: Nikki Fink, Director of Patient Access and Retention Services, PRA Health Sciences
Kate Hersov, MD, Founder, Jumo Health

Oct 19, 2017 Cardiovascular Imaging for Monitoring Safety: Visualizing Outcomes

LifeScience - The goal of this webinar is to discuss the application of cardiovascular imaging when monitoring safety in the development of new medical therapies
Speakers:
Tim Crowe, Director, Cardiovascular Imaging Services, Bioclinica
Bruce Lloyd, MD, Associate Medical Director and Director of Clinical Cardiology Services, Bioclinica

Oct 19, 2017 Treatment Allocation in Randomized Trials: Challenges and Best Practices LifeScience - This webinar will discuss the rationale for the various randomization methods, with illustration from real clinical trials and some considerations about the performance characteristics of the different methods
Speakers:Everardo Saad, MD, Medical Director, International Drug Development Institute (IDDI)
Linda Danielson, MS, Chief Operating Officer, Executive VP, International Drug Development Institute (IDDI)

Oct 23, 2017 Brexit – Separating Fact from Fiction LifeScience -  PCI Clinical Services and its Guests discuss Brexit and its impact on Clinical Trials in the EU and UK
Speakers: Dr. Fiona Withey, Managing Director, UK Clinical Services
Tristram Evans, Quality Director, PCI Clinical Services
Dr. Peter Clarke, SVP CMC, PsiOxus

Oct 24, 2017 Evolving Best Practices for Working with Authors of Scientific Publications – Authorship and Beyond LifeScience - Join the speakers to learn good publication practices that will help to streamline your interactions with scientific authors, while enhancing the quality, efficiency and effectiveness of industry-sponsored research projects
Speakers:
Surendra Sharma, MD, Medical Communications Leader, Spark Therapeutics
Janet Galliera, Executive Director Business Development, PubsHub, an ICON plc company

Oct 24, 2017 Human Whole-Genome Sequencing in the HiSeq X and NovaSeeq™ Era

LifeScience - In this webinar the presenters will give an overview of their large scale WGS library and sequencing pipelines, and improvements made for sequencing on HiSeq X platform and share their experiences on the NovaSeq platform
Speakers:
Robert Fulton, M.S., Director of Development, McDonnell Genome Institute, Washington University
HarshaVardhan Doddapaneni, Ph.D., Assistant Professor, Human Genome Sequencing Center, Baylor College of Medicine

Oct 26, 2017 Clinical Event Adjudication: Comprehensive and Efficient Dossier Review Using a Global On-Line Solution

LifeScience - This presentation will highlight the role electronic expert evaluation plays in improving the quality of endpoint assessments for cardiovascular outcomes. A detailed discussion on the Clinical Event adjudication process workflow will be shared
Speakers:
Lisa Chwieroth, Director of Clinical Event Committee (CEC) Operations, Bioclinica
Souhil Zaim MD, Head of Global Medical and Science Affairs, Bioclinica
Stephen D. Wiviott, MD, FACC, Cardiovascular Division, Brigham and Women's Hospital; Associate Professor of Medicine, Harvard Medical School

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

Oct 27, 2017 Simplify Your Research with A New Generation of High Resolution QTof Mass Spectrometer LifeScience - Current QTOF analyzers that provide resolution >30,000 and mass-to-charge error <5ppm, are generally well suited for HRAM in many aspects, including providing high quality data with no degradation in resolving power or accuracy, making it an excellent match for high resolution separation technologies
Speaker: Robert E. Haufler, Ph.D., Staff Scientist, SCIEX

Oct 30, 2017 Applying ICH GCP E6(R2) Guidelines to All Aspects of Clinical Trials LifeScience -  Key topics for this webinar include how Sponsors can conduct independent verification of the quality and integrity of the data collected from sites, minimize risk for patients, optimize costs through more efficient monitoring, detect trial misconduct, and meet regulatory requirements and follow guidelines related to taking a risk-based approach and interrogation of data 
Speaker: Mark Paul, President North America, CROS NT

Nov 1, 2017 Specific Cardiovascular Issues in Oncology Drug Development LifeScience - This webinar will provide specific recommendations that convey current thinking from regulatory, academic and industry perspectives, with a focus on practical solutions that can be readily implemented in the clinical development arena
Speakers: Polina Voloshko, MD, Chief Medical Officer, BioTelemetry Research
Daniel Goodman, MD, VP, Medical Director, BioTelemetry Research

Nov 1, 2017 Infectious Diseases in the Immunocompromised Host – A Dynamic Landscape with Challenges for Clinical Development LifeScience - This webinar will discuss infectious diseases in the immunocompromised host—with a focus on hematologic malignancies and hematopoietic cell transplantation patients—and the unique challenges for clinical development
Speakers: Hervé Momméja-Marin, MD, Senior Medical Director, Infectious Diseases & Vaccines, Medpace
Anibal Calmaggi, MD, Senior Medical Director, Infectious Diseases & Vaccines, Medpace
Gregory Hale, MD, Senior Medical Director, Hematology & Oncology, Medpace

Nov 2, 2017 The Journey from Passive to Active TMF with C.R. Bard, Inc. and Daiichi Sankyo LifeScience - As the industry continues its move from passive to active model, this webinar features two organizations who are currently on the journey to optimize their TMFs
Speakers: Julia Lombardo, EClinical Applications Manager, C.R. Bard
Jamie Toth, Director and Head of TMF Operations, Daiichi Sankyo
Jason Methia, VP, Vault Clinical, Enterprise, Veeva

Nov 3, 2017 Building Smart Biomedical Devices Using Glass, Lasers, Sensors, and Chips

LifeScience -  This webinar will explain where Glass Core Technology will lead out customers to new products with a higher level of integration and more innovative features that result in smart biomedical devices and other emerging technologies
Speaker: Steve Groothuis, Chief Technology Officer, Samtec Microelectronics

Nov 3, 2017 Simple and Cost-Effective Ways to Engage Patients Using eCOA and IRT Systems LifeScience - A case study will highlight effective use of an IRT system to support patient communications during a clinical trial involving chronic obstructive pulmonary disease
Speakers: Carrie Lewis, MS, Associate Director, Clinical Operations, Lupin, Inc.
Bryan Clayton, President, Strategic Solutions, YPrime

Nov 6, 2017 Drug Name Development: The Regulatory Changes to Know About & How to Prepare for a Successful 2018 LifeScience - This webinar will discusss securing drug name approvals from three major regulatory bodies: FDA, EMA and Health Canada
Speakers from Addison Whitney:
Brittany Scott, Creative Director; Betsy Lard, VP, Managing Director; Barbara Gerber, VP, Managing Director – London; Nancy Kirschbaum, Senior Director, Regulatory Strategy and Consulting

Nov 7, 2017 How to Build Customer Trust, Brand Protection and Sales Using Smart Packaging FoodSafety -  Brand owners are facing new challenges every year and must be able to adapt quickly to competitors, customer feedback, sales trends, brand reputation and trust issues. Discover how smart packaging can create competitive differentiation through consumer authentication and engagement
Speakers: Temogen Hield, CEO, DataDot Technology
Steve Delepine, VP of Business Development, DataTraceID Pty Ltd

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

Nov 15, 2017 Best Practices in Clinical Pharmacology Gap Analysis LifeScience - Viewers will learn how gap analysis can help ensure that development programs will contain all the elements needed to satisfy regulators and investors during all phases of drug development from Investigational New Drug (IND) to NDA
Speaker: Julie Bullock, Senior Director of Consulting Services, Certara

Nov 13, 2017 Conducting Early Phase Oncology Studies - Successfully Moving Through to Proof of Concept and Beyond LifeScience - This webinar will focus on considerations for small, young biotech when selecting a clinical research organisation (CRO) to take their molecule through to proof of concept and beyond
Speakers: Shankar Balaratnam, Associate Medical Director, Simbec-Orion Group
Claire Barton, MD, Orion Clinical Oncology Advisory Board Member

Nov 16, 2017 New Tufts Research: EDC Trends, Insights, and Opportunities LifeScience - Hear new research from Tufts Center for the Study of Drug Development on current and evolving EDC practices across the drug development enterprise
Speakers: Ken Getz, MBA, Director of Sponsored Research Programs & Research Associate Professor, Tufts Study for the Center of Drug Development
Richard Young, Vice President, Veeva Vault EDC, Veeva Systems

Nov 30, 2017 The Pharma Life Cycle: Plagued with Integration and Data Management Challenges, or Opportunities? LifeScience - Learn how to liberate complex data throughout the pharma life cycle to enable innovation as well as sound and timely decision-making
Speaker: Gary Palgon, Vice President, Healthcare and Life Sciences Solutions, Liaison Technologies

Dec 6, 2017 When is Central Imaging Needed in Clinical Trials? LifeScience - This webinar will summarize and highlight the various types of imaging and their role in the clinic and in research, with a perspective on the regulatory aspects that govern its use and practical aspects for pharma, biotech and contract research organizations
Speaker: Souhil Zaim, MD, Head of Global Medical and Science Affairs, Bioclinica

Click here for a list of On Demand Archives

Xtalks Life Science Webinars., 1235 Bay Street, Suite 802 , ON, Toronto, M5R 3K4, Canada
 
Copyright © 2016-2017 Honeycomb Worldwide Inc.