Webinars
Prototyping Randomization and Trial Supply Design
May 21, 2013
10:00 a.m.–11:00 a.m. ET / 15:00–16:00 UK Time
2:00 p.m.–3:00 p.m. ET / 19:00–20:00 UK Time
Join us for this complimentary webinar to learn how Medidata’s randomization and trial supply management (RTSM) solution Medidata Balance® allows for the ability to create interactive prototypes of both randomization and supply management scenarios that can be reviewed and optimized in real time, increasing the overall likelihood of study success.
- Speaker:
David Friend, Senior Business Consultant, Medidata Solutions
Using Technology to Optimize Oncology Trials
May 29, 2013
9:00 a.m.–10:00 a.m. ET / 14:00–15:00 UK Time
12:00 p.m.–1:00 p.m. ET / 17:00–18:00 UK Time
Join us for this one-hour complimentary webinar to hear real-life case studies and learn how today’s advanced technology can benefit cancer research organizations by providing trial efficiency, speed and data visibility.
- Speakers:
Rick Nelson, Vice President and General Manager, Oncology, inVentiv Health Clinical
Richard Young, Director, Regional Sales, EMEA, Medidata Solutions
Risk-Based Monitoring—Adopting a Targeted Approach
June 5, 2013
5:00 a.m.–6:15 a.m. ET / 10:00–11:15 UK Time
9:00 a.m.–10:15 a.m. ET / 14:00–15:15 UK Time
Join us for this free webinar where we will discuss a number of key decisions, processes and budget steps in adopting a risk-based monitoring strategy, focusing on success and failure criteria.
- Speakers:
Andy Lawton, Global Head of Clinical Data Management, Boehringer Ingelheim
Sally Osmond, EVP & General Manager, Cardiovascular & Endocrinology, Clinical Development Post Approval & Strategic Services, INC Research
Richard Young, Director, Regional Sales, Medidata Solutions
How CROs Can Optimize Site Budgeting, Contracting and Payments
June 6, 2013
10:00 a.m.–11:00 a.m. ET / 15:00–16:00 UK Time
2:00 p.m.–3:00 p.m. ET / 19:00–20:00 UK Time
Join us for this complimentary webinar to learn about the latest data-driven tools and techniques which help determine site cost forecasts and detailed grant budgets, as well as facilitate site negotiations and expedite payments. Please note this session is for CROs only.
- Speaker:
Frank Cattie, Vice President, Trial Planning Solutions, Medidata Solutions
Seminars
Optimizing Study Design and Protocol Development
June 11, 2013
South San Francisco, CA
10:00 a.m.–3:15 p.m. PST
We invite you to join us for this complimentary seminar as industry thought leaders discuss the latest industry research on study design and protocol development, delving into why up to a quarter of all procedures conducted during a clinical trial aren't associated with any of the study’s key objectives or endpoints, as well as what our industry can be doing to streamline the study design process.
Register
Optimizing Study Design and Protocol Development
June 12, 2013
Newport Beach, CA
10:00 a.m.–3:15 p.m. PST
We invite you to join us for this complimentary seminar as industry thought leaders discuss the latest industry research on study design and protocol development, delving into why up to a quarter of all procedures conducted during a clinical trial aren't associated with any of the study’s key objectives or endpoints, as well as what our industry can be doing to streamline the study design process.
Register
Improving Data Quality and Streamlining Operations Across the Clinical Lifecycle
June 18, 2013
Copenhagen, Denmark
08:00–14:00 CET
Join us for this seminar as Medidata and other industry experts investigate how a defined, strategic vision for simplifying the collection, management and utilization of clinical data will help us design and execute better trials, maximize on operational, financial and patient opportunities, and reduce trial timelines and costs.
Register
Improving Data Quality and Streamlining Operations Across the Clinical Lifecycle
June 20, 2013
London, UK
08:00–14:00 CET
Join us for this seminar as Medidata and other industry experts investigate how a defined, strategic vision for simplifying the collection, management and utilization of clinical data will help us design and execute better trials, maximize on operational, financial and patient opportunities, and reduce trial timelines and costs.
Register
Industry Events
34th Annual Meeting of the Society for Clinical Trials
May 19–22, 2013
Boston, MA
The Society for Clinical Trials, an international community of professionals from a variety of disciplines involved with the design, conduct and analysis of clinical trials, invites you to join this year’s annual meeting which will include renowned industry speakers, educational workshops and opportunities to learn from experts from around the world.
- Medidata expert Dennis Sweitzer will present, Randomization Metrics: Jointly Assessing Predictability and Efficiency Loss in Randomization Designs.
- Join Medidata expert Sean Neal as he presents, Minimizing Reconciliation Between Safety and Clinical Databases, during the “Safety and Regulatory Insights” session, as well as moderates the “Current Monitoring Practices” session.
Life Science Forum Basel
June 6, 2013
Basel, Switzerland
Medidata is a proud sponsor of this year’s Life Science Forum Basel (LSFB) conference, which attracts more than 100 industry peers to exchange ideas and provide a discussion platform for the communication of the latest developments in the pharmaceutical field.
- Medidata expert Richard Young will present, The Life of a Clinical Data Point: How Thinking of Data’s Role across the Entire Clinical Lifecycle Improves Data Quality and Streamlines Operations.
4th Annual Clinical Trials Summit 2013
June 7, 2013
Mumbai, India
Medidata is excited to exhibit with partner ParadigmIT at this year’s 4th Annual Clinical Trials Summit, where attendees will have the chance to learn, network and benchmark against the global top pharmas and local industry leaders on the best practices in talent, site, budget and performance management in clinical trials.
IATI Bio-Med Israel 2013 Conference
June 10–12, 2013
Tel Aviv, Israel
We are excited to participate in this year’s innovative IATI Bio-Med 2013 conference, which has enabled its participants to help plan the conference agenda and influence its content around biomedical, health care and life sciences topics. Stop by booth #21, where Medidata will be jointly exhibiting with Bioforum Ltd., to learn more about the Medidata Clinical Cloud™, our platform for end-to-end clinical development.
PhUSE Single Day Event
Beerse, Belgium
June 10, 2013
This PhUSE Single Day Event will focus around the theme of “Data Transparency and Submissions Standards.”
- Medidata expert Geoff Low will speak on Underpinning the Underpinning of CDISC—Using the Operational Data Model.
DIA 2013 49th Annual Meeting
June 23–27, 2013
Boston, MA
Once again, Medidata is excited to be a part of this year’s DIA Annual Meeting. Visit Medidata Solutions Booth #805 to learn more about the Medidata Clinical Cloud and how we’re driving the future of clinical trials. Be sure to check out the number of Medidata experts who will be participating in a number of tracks and sessions throughout the conference.
PhUSE Single Day Event
Basel, Switzerland
June 28, 2013
This PhUSE Single Day Event will focus around the theme of “Data Transparency and Submissions Standards.”
- Medidata expert Ian Sparks will present, Data in and out, ODM and WebServices Do the Hokey-Cokey.
If you would like to meet with our experts during one of these events, contact us.