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Archive for the ‘ExL Events News’ Category

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Advances in Drug Delivery Seminar in Boston!

In its seventh year, ExL’s Drug Formulation, Solubility & Bioavailability Summit (March 26–28, 2018, Boston) offers an exclusive, full-day seminar on Advances in Drug Delivery.


Advances in Drug Delivery Seminar Topics

Maintain Necessary Flexibility in the Clinical Testing and Production of Solid Dosage Tablets

Joachim Hoechel, Head, Clinical Pharmacology, BAYER

 

Panel: Achieve Breakthroughs in Oral Biologics Delivery

Moderator: Rakesh Dixit, Vice President, R&D, Global Head Biologics Safety Assessment, MEDIMMUNE

 

Encapsulation and Release of Peptides and Biologics at Higher Loadings Than W/O/W…

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AstraZeneca, Pfizer, Vifor Pharma and More Help Map Out the Best Action Plan for Your Next M&A and Partnering Deal!

At the European Due Diligence Summit for Life Sciences, being held 26–27 February in London, attendees will gain valuable insights from key decision-makers, investors, business development, licensing and alliance management experts from across the pharmaceutical and biotechnology industries. Engage with your peers in a unique learning format consisting of multiple panel discussions and never-before-heard case studies and discover best practices on both buy-side and sell-side transactions from due diligence leaders.


Sessions Built to Address the Challenges of M&A, Licensing and Partnering Deals:
Virtual Due Diligence and How to…

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DOWNLOAD THE BROCHURE for the FiercePharmaMarketing Forum

Download the brochure for the FiercePharmaMarketing Forum, taking place at the Crowne Plaza, Times Square in New York City on March 6–7, 2018, to learn more about successful strategies and best practices in the pharmaceutical marketing space. The significance of a pharmaceutical marketing strategy is paramount to the success of drugs and brands that are introduced to local and global markets. Given recent developments in trends, regulations, and methods, companies must constantly be innovating in order to produce results more effectively than their competition.

Designed by the editors of FiercePharma,…

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Final Week for Early Bird — Regulatory Paths for Expedited Drug Development Conference

Over the last two decades, there have been concerted efforts to increase harmonization across these regulatory bodies and eliminate unnecessary barriers that may delay or otherwise impede the efficient development and production of pharmaceuticals. However, relatively less attention has been paid to harmonization across the expedited pathways.

The Innovative Regulatory Pathways Summit, taking place January 29–30, 2018 in Arlington, VA, is the premier regulatory affairs conference dedicated to global strategies for expediting drug development.


CLICK HERE TO SAVE $200 OFF YOUR REGISTRATION
Andrew Storey, Vice President,…

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DOWNLOAD THE BROCHURE for the Inaugural Cannabis Partnerships Congress

We invite you to DOWNLOAD THE BROCHURE for the inaugural Cannabis Partnerships Congress, taking place March 12–13 at the Hilton San Francisco Airport Bayfront in San Francisco. The Cannabis Partnerships Congress brings together stakeholders involved in Cannabis-based scientific, medicinal, governmental, and research development as to fortify the therapies in a collaborative environment. With the continued enforcement of restrictive policies and regulations on research into the health benefits, it is important for those involved to understand the obstacles in order to enhance product development. This conference will showcase how to overcome legislative hurdles and current and planned cannabinoid…

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Recent Developments Related to Real-Time Benefit Verification

Have you been keeping up with the recent developments related to Real-Time Benefit Verification? Since the release of the brochure, recent news has emerged about one of the biggest pharmacies, CVS Health, that will now be providing real-time insight into medical costs.

Read more on these recent developments right HERE or HERE!

ExL Events’ Real-Time Benefit Verification and Electronic Prior Authorization Forum will discuss the implementation and innovation of real-time benefit verification and how to better enhance electronic prior authorization to…

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FDA Addresses the New Guidances at the 10th REMS Summit

Since the release of ExL Events’ 10th REMS Summit brochure, the FDA has released two guidances that amplify your need to attend the event that has every REMS professional talking. In light of these changes, we are excited to announce the expansion of the 10th Annual REMS Summit program to address the evolving REMS landscape!


TWO BRAND-NEW SESSIONS ADDED!
OVERVIEW OF RECENT FDA GUIDANCES IMPACTING REMS

Gita Toyserkani, Pharm.D., MBA, Regulatory Health Policy Analyst, Division of Risk Management, Office of Medication Error Prevention and…

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Brochure Available: 7th Drug Formulation, Solubility & Bioavailability Summit

When over 80% of APIs in development are poorly water-soluble, drug companies must increasingly rely on new formulation and delivery strategies to maximize bioavailability. ExL Events is proud to announce its 7th Drug Formulation, Solubility & Bioavailability Summit, taking place March 26–28, 2018 in Boston, MA.

We invite you to download the brochure for the leading industry event geared toward helping you identify the precise thresholds when enabled formulations are necessary, as well as determining which methods to use and how to predict and gauge their successes.

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Agenda Released for Disease Awareness Campaigns Forum!

ExL Events is excited to announce the industry’s only event dedicated to strategies for building disease awareness campaigns that educate patients and resonate with healthcare professionals. The Disease Awareness Campaigns Forum is taking place April 4–5, 2018 in Philadelphia. This intimate forum will bring together industry experts and senior-level executives to discuss patient and HCP engagement strategies to build effective disease awareness campaigns to disseminate educational information.

Download the brochure and be one of the first to review the sessions and leading marketing and patient…

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Ensure Inspection Readiness at the 7th Trial Master File Summit

The Trial Master File is the most crucial aspect of a clinical trial for a variety of reasons, and with the TMF industry constantly changing, it is imperative that you also consistently adapt to these developments. The 7th Trial Master File Summit will develop your professional skill set, wherewithal and savvy that you and your company must have to foster an inspection-ready culture while maintaining GCP and quality.

QUICK LINKS:  REGISTER  |  BROCHURE  |  WEBSITE

Register by this Friday, December 1, and mention Discount Code C945BLOG for 15% off registration.

The…

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