Archive for the ‘ExL Events News’ Category
The FDA has taken significant strides to improve REMS in terms of patient safety and access. At the 11th Risk Evaluation & Mitigation Strategies Summit, you will have the opportunity to hear firsthand from the FDA to analyze the patient perspective in regards to specific diseases and their treatments, along with the risks and burdens that are critical to patients.
View the full agenda!
Discuss Patient-Focused Drug Development (PFDD) and Potential Relationships to REMS
Sara Eggers, Operations Research Analyst, U.S. FOOD & DRUG ADMINISTRATION — CDER
Emily Freeman, Ph.D., Director, Risk Management Sciences, ABBVIE
Our adept speaking faculty will deliver insights into…
Friends and colleagues over at PharmaLeaders shared their experience attending ExL Events’ GDPR Update for Global Organization. Dealing with the General Data Protection Regulation (GDPR) since it came into effect in May 2018 is a clear focus for every organization in the industry. That’s why PharmaLeaders agrees that our conference was time and focus well-spent.
U.S. companies who do business with EU residents will be a direct subject to GDPR, as their customers exist under the protections of GDPR. These collaborators and contractors, such as CROs running clinical studies, are required to seek contractual commitments to…
ExL is excited to announce our 3rd European Clinical Quality Oversight Forum, taking place 25–26 February 2019 at the Hilton London Canary Wharf in London, UK.
Download the brochure now!
Click here to register!
David Fryrear, Senior Director, Research and Development Quality Assurance, ABBVIE
REGULATORY UPDATE: MHRA INSPECTIONS
Understand What to Expect During an MHRA Inspection and Know How to Best Prepare
Paula Walker, Inspectorate Unit Manager for GCP/GPvP/GLP, MHRA
GCP RENOVATION – MODERNISATION OF ICH E8 AND E6
Evaluate the Revision of ICH E8 and E6 to Address Evolved Quality Concepts and Critical to Quality Factors
Melissa Mudrick, Vice President and Global Head,…
Ibis Reproductive Health leads the Oral Contraceptives (OCs) Over-the-Counter (OTC) Working Group, which aims to bring the pill OTC, ensuring it’s affordable, covered by insurance, and available to people of all ages. The working group’s statement of purpose (92 organizations and 35 individuals, including the American College of Obstetricians and Gynecologists and the American Academy of Pediatrics) serves as the foundation for its work.
Free the Pill is the working group’s public campaign to educate and engage key audiences in its work to bring a birth control pill OTC in the United States. Learn more about the…
As the chairperson of the 15th Clinical Performance Metrics & Analytics Summit, I would like to invite you to join me in Philadelphia on December 6–7, 2018, for this innovative and collaborative event. More than ever, this year’s Summit will bring together sponsors, CROs, and sites to discuss the importance of using clinical trial performance metrics/key performance indicators to drive decision-making and evaluate the success of those decisions.
ExL, in conjunction with FiercePharma Marketing and Digital Pharma, is delighted to present the 2nd Pharma Marketing Forum — a two-day, educational event, taking place February 25–26, dedicated to showcasing the ways pharmaceutical marketing continues to evolve and the strategies marketers can use to be proactive and innovative in this industry.
BROCHURE NOW AVAILABLE
Senior executives from Teva, Otsuka, UCB, GSK, Roche, and more will be sharing their insights during innovative sessions and 5+ hours of designated networking time.
This holistic event will include comprehensive discussions around all aspects of the pharmaceutical marketing industry with various detailed case studies and interactive panel…
As the chair of the 3rd New Product Planning Summit, I would like to invite you to join us in Boston on December 12–13 for this innovative and collaborative event. This forum is the premier meeting place for attendees to exchange insights and best practices from across the life science industry to optimize the structure and quality of your new product planning groups.
Join me for this two-day event that will discuss how to develop a viable product differentiation strategy, value propositions using clinical endpoints and patient-reported outcomes that can impact payer communications, and go-to-market strategies ahead of a…
Regulatory & Technical Needs of Life Science Usability Pros Met at Human Factors Engineering & Usability Studies Summit
After long delays, 2019 will see the release of new usability standards harmonizing the expectations of FDA and international regulators. What should you expect from these new standards, and how can you begin preparing in advance?
ExL’s 4th Annual Human Factors Engineering & Usability Studies Summit, taking place February 4–5, 2019, in San Francisco, CA, is the only West Coast conference completely devoted to the regulatory and technical needs of life science usability professionals! Our faculty of industry leaders will share all-new analyses not found anywhere else, so save your seat today!
The 3rd Healthcare Ad-Tech & Programmatic Strategy Summit, taking place December 5–6 in Philadelphia, is a not-to-be-missed program covering top strategies to enhance your audience engagement and virtual advertising.
Over the course of one day, attendees will learn:
Using digital marketing in a compliant and effective manner
Balancing privacy concerns with a marketing agenda
Utilizing blockchain as a healthcare professional
Our featured speakers include:
Melissa Rossi, Associate Director, Consumer Media, NOVARTIS
Heidi Padilla, Director, Customer Engagement, GLAXOSMITHKLINE
Kimberly Brenny, Corporate Marketing Director, MEDTRONIC
Orchard Richardson, VP and Managing Director, IAB DATA CENTER OF EXCELLENCE
…and MUCH MORE! Download the brochure to see what you can gain from attending.
The GDPR Update for Global Organization, taking place December 6 in Philadelphia, is a not-to-be-missed program covering the new GDPR regulations specific to clinical trials and clinical research.
Over the course of one day, attendees will learn:
How to establish a strong internal and external SOP to ensure compliance
Preparing for potential data breaches or concern
Navigating GDPR from a global perspective to ensure intelligible consent
…and MUCH MORE!
Download the brochure to see what you can gain from attending.
If you are working in data protection, this is a MUST-attend event. Register by October 26 to take advantage of Early…
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