온디맨드 웨비나

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온디맨드 웨비나

임상시험은 아주 복잡하고 빠르게 바뀌고 있는 중입니다. 이런 환경에서 정보는 가장 큰 경쟁력입니다. 실제 임상시험을 진행하는 것만큼 임상시험의 글로벌 트렌드를 빠르게 파악하는 것도 중요한 상황입니다.

메디데이터는 임상시험을 위한 다양한 솔루션 뿐만 아니라, 정보도 함께 제공합니다. 국내외 전문가들이 전하는 인사이트와 트렌드를 통해 임상시험의 글로벌 추세와 방향을 알아보실 수 있습니다.

 

2021 Medidata Webinar – Decentralized Clinical Trial AtoZ – 분산형 (비대면) 임상시험의 글로벌 트렌드와 적용사례

지금 보기

7월 7일, 메디데이터에서는 최근 가상 임상시험을 넘어 Hot Topic으로 급부상하고 있는 “Decentralized Clinical Trial (DCT)” 즉, “분산형 임상시험”에 대해 Medidata 웨비나를 진행하고자 합니다.

단순한 가상 임상시험이 아닌 Decentralized Clinical Trial (DCT)이 가지는 의미와 필요성 그리고 글로벌 트렌드에 대해서 이야기하고, 메디데이터에서 DCT를 위해 제안할 수 있는 솔루션들과 Accreditated 파트너인 DreamCIS에서 실제 메디데이터의 솔루션을 사용한 고객 사례도 소개하고자 합니다.

  • The Next Clinical Operations: Accelerating Trial Decentralization 김희영, Senior Solution Consultant, Medidata
  • [Case Study] Virtual Clinical Trials with Rave ePRO
  • A. ePRO Build-Up Best Practice 홍성백, IT Director, DreamCIS
  • B. Smarter Operation for Virtual Clinical Trials 손지원, CR Executive Director, DreamCIS

2021 Medidata Webinar – AI와 빅데이터 및 시뮬레이션을 활용한 항암연구의 뉴패러다임

지금 보기

6월 16일, 메디데이터에서는 항암 연구를 진행하고 계시거나 준비하고 계신 제약사 또는 바이오벤처 고객분들을 모시고 Medidata 웨비나를 진행하였습니다.

항암연구에 특화하여 “AI와 빅데이터 및 시뮬레이션을 활용한 항암연구의 뉴패러다임”라는 주제로 메디데이터에서 제안 드릴 수 있는 “시뮬레이션 기반의 항암 타겟물질 발굴”부터 “AI와 빅데이터를 활용한 임상디자인, 합성대조군”에 대해서 이야기하였습니다.

  • Challenge becomes the new strategy(feat. Big data) 김나현 PhD., Acorn AI, Medidata Korea
  • [Case Study] 딥러닝 딥오믹스를 이용한 방사선 저항성 종양 치료제 발굴 및 최적화 사례 김영훈 PhD., CEO, 파미노젠

BIOVIA Webinar – “의약품 제조업체 데이터 완전성(Data Integrity)” 식약처 가이드라인 대응방안

지금 보기

5월 12일 BIOVIA에서는 최근 빈번하게 발생하는 데이터 신뢰성 이슈, 2020년 10월에 발표된 식약처의 “의약품 제조업체 데이터 완전성 평가지침”으로 인해 혼란스러워하는 고객께 도움을 드리고자 웨비나를 진행하였습니다. 고객이 가장 힘들어하고 어려워하는 부분을 해결할 수 있도록 꼭 필요하고 도움이 되는 주제를 선정하여 웨비나를 구성하였으니 꼭 들어보시기 바랍니다.

  • “의약품 제조업체 데이터 완전성 평가지침” 알아보기 – 박영록 Solution Consultant, Biovia
  • QA팀의 데이터 완전성 대응 방안 – 이호상 Solution Sales Specialist, Biovia
  • QC팀과 생산팀의 데이터 완전성 대응 방안 – 박영록 Solution Consultant, Biovia

2021 Clinical Study Cafe – 물질발굴부터 임상연구까지 : 통합플랫폼 전략

지금 보기

메디데이터에서는 임상을 진행하고 계시거나 준비하고 계신 중소 제약사 또는 바이오벤처 고객분들을 모시고 Medidata Clinical Study Café를 진행하였습니다.

금번 행사에서는 길고 복잡한 신약 개발 단계를 위한 “A Unified Platform approach to Life Science (물질발굴부터 임상연구까지 : 통합플랫폼 전략)”이라는 주제로, 신약 개발의 전 과정에서 통합 플랫폼이 주는 최고의 가치를 소개하였으니, 실질적이고 유용한 정보를 얻어가시기 바랍니다.

  • From Discovery to Clinical Research: the unquestioned success in drug development(신약개발의 성공: 물질발굴부터 임상연구까지) – 이준용, Head of Sales
  • Study conduct:the one-stop approach to clinical trial excellence(탁월한 임상시험 운영을 위한 원스탑 솔루션: EDC & RTSM) – 이효백, Solution Consultant
  • Highway to fast enrollment and performance: Acorn AI (빠른 등록률과 기관 성과를 위한 지름길, Acorn AI) – 김나현 PhD., Acorn AI
  • 바이오 신약개발기간 단축을 위한 분자모델링 시뮬레이션 및 디지털 혁신 방법 – 이호상, Solution Sales Specialist, BIOVIA

NEXT+: Medidata NEXT Korea 2020과 새로운 세션까지 추가!

지금 보기

Medidata NEXT Korea 2020을 놓치셨던 분들, 다시 듣고 싶으신 분들 또는 영어 세션을 듣고 싶으신 분들을 위해 준비했습니다. ​NEXT Korea를 통해 기존에 소개해 드렸던 세션들과 함께 NEXT Global의 세션들을 추가로 모두 공개합니다.​

  • 데이터 수집 및 관리 (Data Capture and Management)
  • 임상 운영 및 관리 (Clinical Operation)
  • Acorn AI와 혁신적인 데이터 분석
  • 가상 임상시험 (Virtual Trials)
  • 데이터와 규제

바이오벤처를 위한 웨비나 시리즈: 성공적인 임상시험을 위한 스마트한 결정

지금 보기

바이오벤처에게 꼭 필요한 실무 팁! CRO 선택부터 관리, FDA와 같은 규제 기관과 커뮤니케이션하는 방법 그리고 임상시험에 운영과 관리에 필요한 여러 분야의 주제들로 글로벌 전문가들이 꼭 필요한 정보를 공유합니다.

  • FDA는 여러분의 친구입니다: FDA와 올바르게 소통하는 방법
  • 임상시험 시간을 단축하기 위한 5가지 방법
  • 성공적인 CRO 선택을 위한 5가지 기준
  • 그 외 다수

Reboot Clinical Trials: 코로나19 시대의 변화된 임상시험 환경 및 대응 전략

지금 보기

이 웨비나에서는 메디데이터의 각 영역의 전문가들이 COVID-19 상황에서 전세계 임상 시험의 현황 및 영향에 대해 살펴보고, 환자의 안전성과 임상 데이터의 품질을 유지하면서 임상시험을 지속할 수 있도록 뉴노멀 시대의 임상시험에 대한 인사이트를 드립니다.

  • 코로나 19 가 전 세계 임상 시험에 미치는 영향 및 메디데이터의 전략
  • 코로나 19 시대의 모니터링의 변화 1 : Risk Assessment, Central Monitoring
  • 코로나 19 시대의 모니터링의 변화 2 : The possibility of remote monitoring
  • 코로나 19 시대의 무작위배정 및 임상시험약 공급 관리 : RTSM
  • 코로나 19 시대의 비대면 대상자 중심의 임상시험 : Virtual trials

코로나19 시대에서의 모니터링의 변화: Medidata Remote Source Review

지금 보기

이 웨비나에서는 Remote Monitoring을 위해 꼭 필요한 Remote Source Review에 대해 Medidata의 전문가가 소개와 함께 데모를 진행합니다.

  • Medidata Remote Source Review 소개
  • 데모 및 기능 소개

The Emerging Role of RWE: Longitudinal Patient Insights to Bridge the Clinical and Real World

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This webinar covers how longitudinal patient insights (LPI) can de-risk your clinical trials, lower the costs of follow up studies, and enhance insights.

Budget to Payments: Unify Your Clinical Trial Financial Tools to Streamline Processes

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Join this webinar to engage in the following conversations:

  • Clinical trial financial management elements and connecting the dots with unification
  • Gaining transparency of the full investigator grant budget and payments process and eliminating roadblocks
  • Obtaining the right experts for investigator grant budget and payments processes

Utilizing Patient Centric Solutions to Address Patient Burden in Rare Diseases

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In this webcast, our speakers discuss why it’s so important to include the rare disease patient perspective when developing clinical trials, including:

  • Unique burden patients with rare diseases face in clinical trials
  • Understanding the importance data plays for the patient in trial, and why data return is critical for these patient populations
  • How the design studios Infuse the patient voice in solution design
  • What a patient design studio operates like

Modernizing Data Management in the D-Clinical Age

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Watch this webinar to learn:

  • How to bring trials to patients today by enabling the collection of digital streams from all sources
  • How to discover new technology and processes needed to speed drugs to market
  • How in this new age of D-Clinical, data management can transform clinical trials

Imaging AI and Machine Learning – Beyond the Hype

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Watch this webinar to learn:

  • How AI needs to be focusing in specific areas, as past efforts (IBM Watson) to do everything, have failed
  • How to narrow down imaging problem statements that will generate better results
  • How AI and Machine Learning can function as “guide rails” for radiologists
  • Areas that AI and Machine Learning can increase efficiency (thus saving money) and improve quality (thus saving lives)

Clinical Trial Flexibility & Customization Needs Required by Biotechs & Next Generation Therapies

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After watching this webinar, viewers will:

  • Understand the unique needs of small and midsize biotech companies when conducting oncology studies
  • Recognize the need for an adaptive and responsive CRO amidst the current landscape and increased demand within the growing biotechnology industry
  • Understand CRO best practices for understanding and adapting to the specific needs of small and midsize biotechs
  • Tailor operational and technological approaches to planning, launching and conducting studies for a growing market

Improving Access to Clinical Trials for Rare Disease Patients Through Registries

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Watch this webinar and learn:

  1. Introducing registries as a tool for rare disease patients
  2. Using registries to help rare disease patients become empowered, educated, and engaged regarding clinical trial opportunities

Looking Beyond the Current Trend of Virtual Trials

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Watch this webinar to learn how to leverage many virtualization technologies into a unified approach to trial virtualization and what’s next for virtual clinical trials.

Optimizing Efficiency and Effectiveness with a Data-Driven Clinical Trial Management System (CTMS)

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Watch this webinar and learn:

  • How a data-driven approach to clinical trial management enables effective and efficient oversight of trial activities
  • Strategies for taking a risk-based quality management approach to clinical trial management
  • How the right CTMS can enable better workflows and tighter collaboration across clinical operations teams

Understanding the Novel Challenges in Rare Disease Clinical Development: Perspectives from Experts

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Medidata recently conducted an in-depth market research study with Industry Standard Research to understand how the challenges impacting biopharma and CROs who are conducting rare disease research. Watch this on-demand webinar to learn about:

  • The challenges faced by those working in the rare disease space
  • Their perspectives on how well current technology meets these challenges and what improvements they would like to see in technology or analytics
  • Insights into current or up-and-coming trends in rare disease clinical development

How Five COVID-19 Technology Innovations are Reducing Risk in Clinical Trials

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During COVID-19, regulators and sponsors show pragmatism and flexibility in terms of mitigating challenges in the current climate. The combination of digital distribution, innovation, and flexibility enabled the clinical trial community to expedite drug development during the COVID-19 pandemic while also minimizing risks to patient and trial success. Watch this on-demand webinar to explore how new and reimagined technology innovations are addressing the impact of COVID-19.

Tackling the Challenges in Development and Clinical Adoption of Advanced Therapies

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Watch this webinar to hear about the perspectives of key stakeholders on the challenges in designing Advanced Therapy Medicinal Product (ATMP) clinical trials with small patient populations, reimbursement uncertainty, and long term prospects for the commercialization of advanced therapies

[Webinar Series] The Changing Landscape of Clinical Trials

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Traditional ways in which clinical trials are being conducted are being put to the test and having repercussions across the clinical trials landscape as COVID-19 continues to disrupt the world.

Watch this series of on-demand webinars where we discuss this rapidly changing situation, what you can do to manage trials more effectively and the role that technology can play to work together to vastly simplify trial management.

Next Virtual Event: Pharma & Biotech

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Watch Medidata’s Virtual Conference On Demand where experts discuss:

  • Risk Assessment, Central Monitoring, and RTSM
  • Patient Centricity by Design: The Path to Patient-Centric Solutions
  • Enabling Clinical Trials in a Pandemic: Continue Treating Patients and Minimize Risk

NEXT Virtual Event: Medical Device & Diagnostics

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Watch Medidata’s Virtual Conference On Demand where experts discuss:

  • eConsent – A Patient-Centered Approach Towards Improving the Informed Consent Process
  • RTSM and Medical Device Trials: Realizing the Power of a Unified Platform
  • Virtual Human Modeling: The Living Heart
  • Connecting the Next Generation of Patient Data and Devices with Deep Analytics

NEXT Virtual Event: CRO

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Watch Medidata’s Virtual Conference On Demand where experts discuss:

  • eConsent – A Patient-Centered Approach Towards Improving the Informed Consent Process
  • RTSM and Medical Device Trials: Realizing the Power of a Unified Platform
  • Virtual Human Modeling: The Living Heart
  • Connecting the Next Generation of Patient Data and Devices with Deep Analytics

[MassMedic Series] The New World: Connecting the Next Generation of Patient Data and Devices with Deep Analytics for Commercial Success

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Watch this webinar to learn about a use case on the process of building the standardized, multi-faceted dataset to enable deep real-world data analysis for pre-surgical population management, surgical treatment patterns, and post-operative outcomes assessment.

[MassMedic Series] RTSM & Remote Monitoring: Realizing Quality while Mitigating Study and Site Risk for Medical Device Trials

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Watch this webinar to hear Medidata experts discuss the challenges in device supply management and remote monitoring to realize quality while mitigating study and site risk during these challenging times.

[MassMedic Series] Reconsidering Trial Design Medical Device Companies to Ensure Data Capture in the Challenging COVID-19 Era

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Watch this webinar to learn about considerations for adjusting data collection strategies in the middle of ongoing studies, plus trial virtualization, and how the move to decentralization will only accelerate in a post-COVID-19 world.

Virtualizing Clinical Trials: The Impact of Technology on the Patient Journey

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Watch this webinar to hear about the patient’s journey and the impact of virtualizing technologies such as direct to patient trial supply management (IMP), eConsent, and other remote data capturing tools all integrated on a unified platform.

COVID-19 and Clinical Trials: Support Risk Mitigation and Recovery Plans With Data and Analytics

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Watch this webinar to learn about key considerations for managing clinical trials during these turbulent times and how industry-wide trial metrics and analytics can support:

  • Situation tracking by geography and therapeutic area
  • Impact assessments and scenario analyses at trial and portfolio level
  • Identification of leading indicators of recovery

Transforming Clinical Development and Discovery with Multi-omic Data in the Era of Precision Medicine

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Watch this webinar to hear industry experts discuss key challenges, propose best practices, and share success stories illustrating how incorporating translational omics data into clinical development yielded novel insights and improved patient/study outcomes.

Maximizing the Benefits of a Unified Clinical Data Capture and Management Platform

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Watch this webinar to see how leveraging multiple solutions on a unified platform streamlines processes, drives operational efficiency, eliminates reconciliation, and provides faster data insights.

Driving Quantitative Image Analysis for Early Phase Clinical Trials with Medidata and Medpace

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Watch this webinar to hear experts from Medidata and Medpace discuss the role of Quantitative Imaging Biomarkers in clinical trials.

End of Study Hacks: The New Digital Age

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Watch this webinar to learn how Sponsors and CROs are challenging the status quo by developing new models to improve end of study compliance and productivity.

COVID-19: A New Era Transforming the Clinical Trial Landscape

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Watch this webinar to learn about the changing regulatory environment with respect to clinical trials in COVID-19 world, the impact of COVID-19 on trials, trial participants, sponsors, partners, and solutions to support this challenging new era.

Clinical Trials in a Post Pandemic Era

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Watch this OnDemand webinar on the future of Clinical Trials in a Post Pandemic Era moderated by Professor Stan Kachnowski, Director of the Digital Health Strategy program at Columbia Business School.

Medidata Office Hours Series

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AS COVID-19 continues to spread, Sponsors and CROs are struggling to continue trials while maintaining patient safety and data integrity. Watch these On-Demand webinars to hear Medidata’s panel of experts discuss trial virtualization, remote consent, and rapid eCOA deployment models that will help maintain the forward momentum of your clinical trials.

Declutter the Data in your Clinical Trial: Mitigate Risk Before it Becomes an Issue

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In this webinar, you’ll hear a discussion and Q&A Chat on how to find errors, trends, and anomalies in data—through a number of statistical algorithms and tests that do not require programming—while integrating this process as part of your risk process improvement.

Clinical Trial Data Meets the Real World: Bridging the Experimental and Post-Launch Worlds

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In this webinar, you’ll hear about key considerations and best practices when combining clinical trial data with real world data to power big data analytics.

Medical Devices and Advanced Analytics: Delivering on the Promise of Connected Data

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Watch our webinar and Q&A session where we will demonstrate how Acorn AI’s Connected Patient Platform can bring insight into the vast stores of video, imaging, and electronic surgical notes created by the new generation of robotic, precision, and surgical devices.

Unleash the Power of an Integrated Imaging/EDC Platform

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In this webinar, you’ll discover what an integrated solution looks like and how it could power up your trial by reducing time and eliminating errors on data reconciliation and double data entry.

CIOs’ Perspectives: Driving Clinical Trial Innovation with a Unified Platform

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In this IT-focused webinar, you’ll hear about the need for a platform approach to clinical research, the rationale for switching from disparate systems to a unified platform, and the benefits that could be realized with a unified platform.

Synthetic Controls: Best Practices and Regulatory Perspectives

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With fewer than 10% of compounds successfully achieving Phase 1 to FDA approval status1, researchers are increasingly seeking data and methods to address key challenges.

In this 1-hour session, you will hear from former FDA leaders and industry experts.

1Source: Clinical Development Succes Rates 2006-2015, BIO Biomedtracker, Amplion

Improving Clinical Trial Quality with Best Practices for E-Clinical Technology

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The increasing challenges of clinical research are well-known; growing trial complexity, more data sources and data points, disparate systems, manual processes and more. Watch this on-demand discussion on the new strategy for managing clinical trial technology.

A Paradigm Shift to Realize Intelligent Clinical Trial Oversight

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The usual approach of adding technology and headcount to manage today’s clinical trials is not sustainable or scalable. Learn how Rave CTMS delivers expected efficiencies and more importantly, enables you to be effective.

How and Why Celgene Adopted Medidata Rave eCOA

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This incredibly informative webinar delves deeply into Celgene’s adoption of Medidata eCOA solution. If your company is looking to adopt a new eCOA solution or have issues with your current one, this webinar is a must watch.

Applying Unified E-clinical Technologies to Streamline Study Conduct

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In this webinar, Medidata will conduct an interactive demo of our intelligent platform for life sciences—exploring our broader EDC, RTSM and ePRO capabilities—and show how adopting one platform can help unify your data and workflows across study execution, allowing for rapid study startup, more streamlined execution with cleaner data, and the elimination of unnecessary reconciliation efforts.

Improving Patient Centricity with Edge Design Optimizer

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In this demo webcast, see firsthand how Rave Design Optimizer can help you improve trial execution by identifying opportunities to optimize protocol design and bolster or reinforce patient retention strategies, leading to a more patient-centric trial.

Fast Track Your Early Clinical Development Lifecycle

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Discover how early-stage solutions can give you the competitive edge you need to accelerate your clinical development lifecycle.

The New Model for eCOA: Modernizing Technology, Process and Science to Change The Game

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Join industry experts from Medidata and Syneos Health as they discuss a long-awaited new path forward to the implementation of eCOA with a solid foundation of technology, service and science.

Global Site Payments; How Clear is Your Financial View?

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Now more than ever, clinical trial sponsors and CROs share a common burden – accurate budgeting, financial planning, and timely planning. Learn how to improve financial health, fuel innovation and increase compliance with the Medidata automatic payment solution.

Utilizing a Technology-first Approach to Maximize Brand Value & Gain Competitive Advantage

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In this webinar, we highlight some of these approaches and demonstrate how data and analytics can be used to gain a competitive advantage and create differentiation.

The Promise of Real-World Data: Using Technology to Enable the Standardization, Transparency, & Replicability of RWD Research

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Watch this webinar to learn how the use of technology for deploying data and analytic standards can be utilized to meet this challenge, by facilitating the standardization, transparency, reproducibility, and replicability of RWD research.

Unified Platform Defined

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Learn the five characteristics of a unified platform and how each benefits clinical research both for a single trial and across your suite of research efforts.