Archive for the ‘ExL Events News’ Category
The 3rd Product Complaints Forum, taking place March 25–26 in Philadelphia, is a not-to-be-missed program covering top strategies to enhance your entire complaints processing system. Early Bird Pricing Ends THIS Friday, February 8!
Over the course of two days, attendees will:
Discuss hot-button issues within Pharma/Biotech and Medical Device industry-specific sessions
Master the key industry regulation changes and requirements anticipated globally for 2019–2020
Learn optimal procedures for trending, reporting, and complaint handling procedures
Explore organizational tactics that will ensure smooth transitions between complaints, recalls, and quality systems
ExL Events is pleased to announce that the agenda has been released for the 6th Promotional Review Committee Compliance & Best Practices — Midwest, taking place May 15–17, 2019, at the Kimpton Hotel Palomar Chicago. Join industry experts at the ONLY VENUE for sharing expertise on review committee composition and leadership methods.
BROCHURE IS NOW AVAILABLE
With so many perspectives and tight deadlines, promotional review committees are tough to manage, even under the best circumstances. More frequently, PRC professionals are facing new and uncertain challenges coming from interpersonal disagreements, unclear leadership responsibilities, staff turnover, and ever-evolving…
The 2nd Pharma Marketing Forum is just a few weeks away! Co-presented by FiercePharma Marketing and Digital Pharma, our program features industry leaders with senior-level experience from Humana, Pfizer, Google, Roche, BMS, Walgreens, and many other organizations! Don’t miss out on the chance to learn from experts who continue to evolve in the fast-changing and innovative industry. Click here to view the agenda!
Cozi Namer, Healthcare Industry Development Lead, GOOGLE
Judy Berei, Excedrin Global Brand Lead, GSK CONSUMER HEALTHCARE
Claudia Bujold, Vice President, Marketing, REATA PHARMACEUTICALS
Holly Campbell, Deputy Vice President, Public Affairs, PhRMA
Kimberly Coleman Clotman, Senior Director, Marketing, NABRIVA THERAPEUTICS
Alexis Denny, Director of Government Affairs, PKD FOUNDATION
Shira D’Erasmo, Head of Communications, HUMANA HEALTHCARE…
In order to properly navigate through the obstacles of medical device regulations, sponsor organizations must identify specific reports for adverse events related to the device and also relay any safety issues in regards to the device.
For this reason, ExL Events is excited to announce that Michael Drues, President of Vascular Sciences, and Richard Arriaga, Sr. Director and Head of Case Processing at Pfizer, are co-chairing the Medical Device Safety & Reporting Summit on March 25–26 in Philadelphia. Michael and Richard will guide through two full days with an expert speaking faculty discussing proactive methods to ensure device safety while remaining compliant with established regulations…
If you plan on improving your TMF document management and your TMF’s inspection readiness, then the four courses of the TMF Institute — Frankfurt are your best resource in Q1 to strengthen your skill set. The Early Bird discount is expiring — this is the last week to save €150 on registration! Register NOW!
Regardless of the level of achievement, position, title, or area of responsibility, every professional is responsible for Inspection Readiness. Each of the following courses at this institute is customised to meet the needs for professional growth and education of a particular audience in the TMF…
If you haven’t already reserved your seat for the Life Science Compassionate Access Summit, taking place March 18–19 in Philadelphia, the Early Bird deadline is quickly approaching — Register NOW!
Early Bird rates expire this Friday, February 1!
Signing up prior to the Early Bird’s expiration will give you access to a $200 discount on your registration. Join companies like UCB, Shire, and Retrophin to discuss the different outlooks and ethical approaches to compassionate use requests.
At this two-day, educational and networking event, attendees will be…
This is the last week to receive $200 off the standard registration rate for the 2nd Adaptive Clinical Trials Symposium, taking place March 18–19 in Philadelphia. Early Bird rates expire this Friday, February 1! Register NOW!
This event will encompass all that is adaptive design; that includes planning and managing an adaptive trial, FDA guidance and tips to navigate through the gray areas associated with an adaptive design, the role of interim analysis in adaptive design, and much more! Attendees will leave with effective…
Early Bird Pricing for the 10th Proactive GCP Compliance Conference Ends THIS Friday, February 1! REGISTER TODAY and learn from the following sessions, each mapped to their relevant section of ICH E6 R2, on March 18–20 in Philadelphia.
RISK IDENTIFICATION (ICH E6 R2 5.0.1 & 5.0.2)
Identify Critical Processes and Data, and Their Associated Risks
Cheryl McCarthy, RQAP-GCP, CQA, CBA, Associate Director, R&D Quality and Compliance, BIOGEN
RISK CONTROL AND COMMUNICATION (ICH E6 R2 5.0.4 & 5.0.5)
Define Quality Tolerance Limits and Effectively Communicate These Parameters
Celeste M. Gonzalez, B.S., CVT, RQAP-GCP, CCRP, Principal Specialist, Clinical Quality Assurance, BOSTON SCIENTIFIC
In a recent guest column over on Clinical Leader, Audrey Rossow (A Rossow Consulting, LLC) discussed her findings from job searches using the term “trial master file,” revealing the needed skills for managing an eTMF. You’d think that the listings she found would be quite similar, if not the same in regards to the requirements and skills needed to apply for these positions, but you’d actually be incorrect!
Rossow’s article breaks down the types of positions that come up in this search (including TMF Associate/Coordinator/Manager/Specialist, Clinical Project Associate, and more), and how these listings spelled out…
Before he takes that podium at our Medicare Conference 2019, Co-Founder of BETTERDOCTOR and Chief Executive Officer of QUEST ANALYTICS, Ari Tulla, sat down with ExL Events to discuss provider-direct accuracy. Take a look!
READ THE INTERVIEW HERE
ExL’s Medicare Conference will arm attendees with methods and strategies to improve the quality, ratings, member engagement and health system alignment of your Medicare Advantage and/or Dual Eligibles program. Speakers representing health plans, regulatory agencies, and health systems will share experiences and…
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