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Archive for the ‘ExL Events News’ Category

MASS West 2019 Early Bird Pricing Expires This Week!

Don’t miss this last discounted opportunity to join your colleagues at MASS West 2019, taking place September 23–25 in San Diego, CA! This unique event addresses the strategic and operational challenges facing medical affairs, MSL managers, and field medical professionals, and provides attendees with takeaways designed to improve these functions. 

This is the last week for Early Bird pricing! REGISTER NOW

Reserve your seat and take advantage of these Early Bird savings of $200 and register your team by this Friday, August 16!

This is the leading industry event that provides practical insights and actionable solutions for…

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Co-Chair Message: 8th European TMF Summit

One of this year’s highly experienced co-chairs, PhlexGlobal’s Chief Strategy Officer, Karen Roy, has a message for the TMF community. Karen will join the expert speaking faculty and like-minded attendees of ExL’s 8th European TMF Summit as they combine forces and explore actionable lessons, replicable strategies, and vast networking opportunities. The three-day Summit features two workshops, 15 case studies, more than 35 speakers, and 10+ hours of networking with 150 peers who share the same responsibilities and challenges. I urge you to download the agenda and review all the speakers, tracks, and topics being offered.

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Chairpersons’ Message: 3rd Disclosure and Transparency for Clinical Data Summit

As chairpersons of the 3rd Disclosure and Transparency for Clinical Data Summit, we would like to extend an invitation for you to join us from across the industry to define standardization processes for trial disclosure and registry, provide best practices to balance commercial confidentiality and public access, and examine proven tactics that facilitate data sharing and preserves data usage while ensuring anonymization. We are excited to discuss the tools needed to maximize the benefits of clinical data from the inherent risks of clinical trials, all while complying with national and global disclosure compliance regulations.

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Lead Course Instructor, Jamie Toth, Discusses TMF Institute — Philadelphia

When I was asked to take part in the first TMF Institute held in 2018, I was thrilled! The idea of key courses on TMF topics held in an 8-hour, presentation-type session with group discussions and the opportunity for sharing best practices was exactly what the industry needed!

I am once again excited to be part of this valuable industry learning event at the TMF Institute — Philadelphia on August 12–13.

This year, I will be the lead instructor on the Ensure Compliant Documentation Course, where we will be discussing how to align processes with the work of TMF contributors to…

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JUST ANNOUNCED: The Digital Therapeutics Strategic Partnerships Summit

ExL Events would like to announce The Digital Therapeutics Strategic Partnerships Summit, taking place on November 4–5 in Los Angeles. With the rapidly developing landscape in the industry of digital therapeutics, we have brought together trailblazers from each stakeholder segment to take a deep dive into some of the industry’s most pressing topics.

Conference co-chairs, Joel Sangerman of Click Therapeutics and Ruchita Sinha of Sanofi Ventures, are just two of the expert leaders that comprise the speaking faculty. The Summit will feature real-world lessons learned through case studies, in-depth sessions, and diverse panel discussions directly from the people involved in some of the most successful strategic…

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Q&A – Medical device marketers highlight what’s next in the industry

ExL had the pleasure of speaking with several members of our speaking faculty, who’ll be on hand to present at this year’s 9th Digital Marketing for Medical Devices conference on August 5–7 in Minneapolis, MN. We asked each medical devices marketing professional how they think the industry has evolved, the challenges they continue to face and emerging technologies – topics that will be highlighted during the event. Download a copy of the program agenda to review.

Speakers Victorria Wytcherley, Senior Marketing, Digital Marketing Lead, PHILIPS, Liz Presson, Digital Media and Community Experience, OTICON MEDICAL and Nick Wanliss , Digital Marketing Specialist,…

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What Do Tom Cruise and TMF Management Have in Common?

RISKY BUSINESS.
Clinical trial document management is no joking matter! As a TMF professional, you understand the seriousness and weight held by compliant and complete study files. So, how does your organization identify risk within your TMF processes?

ExL’s Trial Master File Institute — Philadelphia features a full-day workshop focused on developing and executing strategic plans that can correct gaps in the completeness, non-compliance, and quality of your organization’s TMF processes. Lead instructor Donna Dorozinsky, President of Just In Time GCP, has prepared a robust workshop that will arm attendees with strategic approaches for correcting some of the most common…

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Chair Message: 9th CMO Quality Oversight and Risk Management Summit

Like you, I have had many opportunities to attend conferences, but I selectively decide to focus on events that will add immediate and long-term value to my organization and its evolution. I also want to ensure that events are aligned with my personal values as a leader.

For that reason, I have accepted the opportunity to Chair the 9th CMO Quality Oversight and Risk Management Summit this September in Boston, MA. This conference will help Quality professionals enhance the collaboration between sponsors and CMOs by understanding the complexities of risk management, quality systems, and stakeholder relationships.

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As…

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How Much Do You Know About Disruptive Technologies in TMF?

It is no secret that technology has improved the efficiency, Quality, and process of reporting in clinical trials. Given the ever-advancing nature of technology, one of the tracks at our 8th European TMF Summit focuses on disruptive technologies in the industry. Not only will the Summit cover some of the newest trends in digital advancement, but we will dive deep into multiple case studies from Novartis, Bayer, Novo Nordisk, and more to offer attendees an analysis of the tech innovations in TMF.
Featured Sessions
Novartis Case Study: Use AI for Document Migration and Document Management
Matthias Wittig, TMF Business Lead Consultant, ARCONDIS

Leverage…

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Are You Staying up to Date With All the Regulatory Tools and Changes for Submissions?

Given the constant evolution of U.S. and international regulations and guidance, submissions teams need to stay up to date with the necessary tools and technologies to be as efficient as possible. On July 9–10, the 3rd eRegulatory Submissions Summit will provide you with a better understanding of format requirements for eCTD and learn how organizations are staying compliant while working in this new format.

Download the Brochure Now!
Join your colleagues next month in Philadelphia, PA, and take advantage of…

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