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Upcoming Life Science Webinars

  Date Webinar Title Synopsis

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: Rob Nichols, Chief Commercial Officer, Director, Algorics
Giulia Zardi, Biostatistician, CROS NT

Oct 30, 2017 Efficiently Managing Your Drug Supply Beyond IRT LifeScience - Learn about the benefits of using a supply management tool that enables global inventory management across a sponsor’s entire portfolio starting from brite stock through destruction
Speaker: Brett Castano, Senior Architect, Project Management, endpoint Clinical

Oct 31, 2017 How Leveraging an Asia-Pacific Network Can Create Regional Efficiencies in Clinical Supply Management LifeScience - In this webinar, our featured speaker will explore how to leverage the major clinical supply centers of China, Singapore and Japan to support clinical trials within the Asia-Pacific region for both local and global study sponsors
Speaker: Daniel Gao, Site Director, Clinical Supply Services – Shanghai, Catalent

Nov 1, 2017 Key Takeaways from the New CSRC/FDA Meeting on Cardiac Safety and Cardiovascular Safety Issues in Oncology Drug Development LifeScience - In this webinar learn about the updates from the new CSRC/FDA meeting on cardiac safety and cardiovascular safety issues in oncology drug development to optimize your clinical trial.
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 Research Inc.
Bryan Clayton, Vice 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 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 8, 2017 Delivering Efficiencies via the Functional Service Provider Model for Investigator Payments LifeScience - The speakers will discuss some of the best practices and crucial elements for executing successful FSP engagements specifically for site payments
Speakers: Victoria Moore, FCCA Executive Director Global Business Finance, INC Research/inVentiv Health
Shaun Williams, Senior Director, Investigator Payments, INC Research/inVentiv Health

Nov 9, 2017 First-In-Human Studies – An Examination of the Evolving Regulatory and Clinical Practices LifeScience - In this webinar, INC Research/inVentiv Health experts will discuss the evolving regulatory and clinical requirements to ensure safety and compliance when conducting First-in-Human studies
Speakers: John Oldenhof, PhD, Executive Director, Clinical Pharmacology, Early Phase, INC Research/inVentiv Health
Richard Larouche, VP Medical Affairs, Early Stage Clinical Operations, INC Research/inVentiv Health
Clark Williard, Executive Director, Bioanalysis, Early Stage Bioanalytical Labs, INC Research/inVentiv Health

Nov 13, 2017 Conducting Early Phase Oncology Studies - Successfully Moving Through to Proof of Concept and Beyond LifeScience - This one-hour webinar will focus on strategic considerations for the molecule, including a brief review of the dynamic research landscape of oncology drug development, patient recruitment and product development aspects.
Speakers: Shankar Balaratnam, MBBS, MSc, MRCS, MFPM, Associate Medical Director, Simbec-Orion Group
Claire Barton, MA, MB, BChir, MRCP, PhD, FFPM, Orion Clinical Oncology Advisory Board Member
Chirag Patel, Director of Regulatory Affairs & Technical Writing, Simbec-Orion Group

Nov 14, 2017 A Vast Unmet Need: Challenges in Alzheimer’s Clinical Trials LifeScience - This webinar will review the current global pipeline of Alzheimer’s trials and their geographic locations, describe innovations in trial design, and promote consideration of optimal clinical trial processes, including preclinical patient populations, clinical assessments sensitive to the earliest disease-related changes, and biomarkers as outcomes of clinical trials
Speakers: Krista Armstrong, Vice President & Head of Neuroscience, Premier Research
Sebastian Turek, Project Director, Premier Research

Nov 14, 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 15, 2017 Rare Disease Disorders and CNS Drug Development – Paving the Way for Precision Medicine LifeScience - Topics include the shifting clinical development landscape, the history of treatment of rare diseases with CNS manifestations, operational lessons-learned in identifying, enrolling and retaining rare disease populations in clinical trials, and new approaches to deliver disease specific targeted therapies to the CNS
Speakers: James Vornov, MD, PhD, Vice President of Medical Affairs, Neurology, Medpace
Richard Scheyer, MD, Vice President of Medical Affairs, Neurology, Pharmacology, Medpace
Terence Eagleton, MBBS, BSc, Senior Medical Director, Rare Diseases, Medpace
Michelle Petersen, MS, Sr. Associate Director, Clinical Trial Management, Medpace

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 Center for the Study of Drug Development
Richard Young, Vice President, Veeva Vault EDC, Veeva Systems

Nov 17, 2017 Neuroprotective Treatment Strategies in Multiple Sclerosis LifeScience - The speakers will discuss the latest neuroprotective treatment strategies in multiple sclerosis (MS)
Speakers: Manuel Friese, MD, Professor of Neuroimmunology and Director of the Institute of Neuroimmunology and Multiple Sclerosis (INIMS), University Medical Center Hamburg-Eppendorf
Stephen Hess, PhD, Research Leader, Ion Channels, Evotec AG

Nov 17, 2017 Real World Evidence Across the Product Life Cycle: Regulatory and Payer Landscape LifeScience - This webinar will discuss how real world evidence is playing a larger role across the entire product life cycle, with a focus on late phase regulatory discussions and payer decision-making
Speakers: Jane Turner, Senior Principal, Real World Evidence, ICON
Guy Sherwin, Lead Consultant, EU Pricing and Market Access, Commercialisation and Outcomes, ICON

Nov 21, 2017 Multiplex IHC Immuno-Oncology Panel LifeScience - This webinar will discuss standardized profiling of the immune status based on spatial and functional characterization of the tumor microenvironment
Speaker: Dr. Svenja Lippok, Product Marketing Manager, Definiens AG

Nov 28, 2017 Removing Risk from Clinical Trial Management System (CTMS) Implementations

LifeScience - This webinar will demonstrate how organizations can mitigate many of the common risks and challenges of implementing CTMS systems by starting with a small, limited implementation
Justin Hunt, Director, CTMS Implementation Services, Bioclinica

Nov 29, 2017 Achieving Operational Excellence in the Lab

LifeScience - Join our webinar to find out how Bayer uses E-WorkBook to improve lab practices, increase laboratory efficiency and build a laboratory environment suited for business needs both now and in the future
Oliver Hesse, Director Lab Automation & Data Management, Bayer Healthcare LLC
Will Scott, Senior Consultant, IDBS

Nov 29, 2017 Techsol Oracle Argus Safety Cloud and E2B R3 Upgrade Accelerator for Emerging Biopharma Companies

LifeScience - The speakers will describe and demonstrate how emerging life science companies can take advantage of a market-leading safety solution - Argus Safety cloud
Speakers from Techsol Corporation:
Kim Pomphrett, Associate Vice President Client Partner
Sriram Varma, Head of Global Services
Satya Sagi, Founder & CEO

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

Nov 30, 2017 Born on eCOA: The New Standards of Deployment

LifeScience - This webinar will discuss the advantages of COA development directly on an electronic platform, completely eliminating the steps and cost involved with migration
Speakers: Catherine Aquadro, MD, Head of Thought Leadershi, Mapi
Donna Mongiello, RN, BSN, Vice President, Strategic Solutions, YPrime

Dec 4, 2017 Reinvigorating Kidney Disease R&D: Latest Innovations Aim to Address Vast Unmet Need LifeScience - This webinar will examine new and more advanced and personalized precision medicine approaches to kidney disease research, including both potential drugs and technologies
Speaker: Eric B. Grossman, MD, Vice President and Medical Director, Clinipace Worldwide

Dec 5, 2017 Deciphering the Complexity of the Acute Leukemia Immunological Microenvironment with 3D Biology™ Technology LifeScience - Learn more about how the combined analysis of SNV, mRNA, and protein expression on the nCounter system enabled a comprehensive characterization of the molecular landscape of leukemia cells
Speakers: Doug Hinerfeld, Ph.D., Principal Product Application Scientist, NanoString Technologies
Sergio Rutella, M.D., Ph.D,, Professor of Cancer Immunotherapy, John van Geest Cancer Research Centre, Nottingham Trent University

Dec 5, 2017 AImproving Regulatory and Operational Performance in Orphan Drug Development LifeScience -  This webinar will discuss the regulatory and operational nuances of orphan drug development, the benefits of early planning and engagement and how to operationalize their regulatory strategy
Speakers: Kimberly Glen, Executive Director, Rare Diseases, Premier Research
Nach Davé, Vice President, Global Regulatory Affairs, Premier Research

Dec 5, 2017 Effective Implementation of the Revised EMA First-in-Human (FIH) Guidance to Accelerate Your Early Clinical Development LifeScience - This webinar will cover the key aspects of the revised guidance in relation to early phase regulatory strategy
Speakers: Dr. Annelize Koch, MBChB, FFPM, Medical Director, Simbec Research
Dr. Simon Hutchings, MPharmacol PhD CHP, Director Scientific Affairs, Simbec Research

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

Dec 6, 2017 Global Medical Information System: Characteristics & Implementation Approach

LifeScience - The speakers will examine key characteristics of a global medical information management system and the critical factors that drive an optimized implementation and deployment strategy
Speakers: Saad Rahman, Head of Product Management, Techsol Corporation
Kevin Shea, Director Strategic Advisory, Techsol Corporation

Dec 7, 2017 US FDA Advisory Panel Meetings: Strategies to Maximize Success LifeScience - To better understand how to effectively prepare and plan for successful Advisory Panel meetings, NAMSA will present a webinar on strategies for working with the FDA for medical device manufacturers
Speaker: Chris Mullin, Director of Product Development Strategy, NAMSA

Dec 11, 2017 Clinical Supply Chain Management: Experience Matters

LifeScience - When the unanticipated problem comes up, having a strong supply manager on board with a background in clinical supplies and access to a network of other supply managers, can be the difference between missing milestones or moving the trial forward with little to no patient and trial impact
Speaker: Sylvia Tsengouras, Senior Clinical Supply Chain Manager, Fisher Clinical Services

Dec 13, 2017 A Comprehensive Endocrine Disruptor Screening Program: A VTG ELISA that Preserves the Fish

LifeScience - This webinar will describe the background associated with the development of this assay, how it can be used as a part of a comprehensive endocrine disruptorscreening program and future directions utilizing fish mucus samples to measure related endpoint proteins
Speaker: Reinhard Möller, PhD , Sales & Marketing Manager, TECOmedical AG

Jan 23, 2018 Schizophrenia Trials: Overcoming Methodological Challenges to Enhance Study Success LifeScience - This webinar will consider methodological improvements associated with recruiting patients into clinical trials, improving patient assessment and retention in trials, the use of cognitive biomarkers to guide decision making about the safety and efficacy of drugs and how to minimize the risk of placebo and practice effects in studies of schizophrenia
Speaker: Dr. Kiri Granger, Director of Neuroscience, Cambridge Cognition

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