Join us September 12-13 for an unequaled look far beyond the paper functions of programs and into gauging pull- through and effectiveness at eliminating risk. No other event offers as much detail on effective communication with safety teams, selecting and cooperating with vendors, and keeping up with technological and regulatory changes that impact risk management and pharmacovigilance.

Women executives in pharma and healthcare who have climbed every obstacle to get to the top share their success stories to educate and inspire the next generation of leaders. This program challenges and guides attendees to empower women in leadership roles and continue to close the gender parity industry gap.

Virtual clinical trials, a reliance on telemedicine and remote monitoring have brought many changes to clinical trials. Adapting to the ever-changing landscape requires flexibility when crafting and modifying clinical trial agreements. DGE’s 3rd Clinical Trial Agreements Forum is designed to walk you through important changes impacting CTAs including incorporating cybersecurity language, more complicated indemnification, complexities of third party contracting and an increase in remote monitoring. The conference agenda provides insight into industry best practices and legal and technological trends impacting success plus ways to expedite contracting and study start up.

A strong omnichannel marketing campaign allows pharma to reach the right people, in the right place, with the right message. By prioritizing promotional spending based on previous impact and consumer data, marketers can truly optimize their investment. But do you have the technology and data necessary to make your marketing as successful as it could be?
 

Explore critical tracks at DeviceTalks West like, Innovation & Investment, Prototype & Product Development, Manufacturing & Supply Chain, Regulatory & Reimbursement and Better Tools & Technologies

Join us at DeviceTalks West in Santa Clara, CA on October 19th and 20th! Register here for your conference pass: https://cvent.me/rD9AbZ?RefId=MT

The old models for launches are undergoing disruptive transformation to accelerate speed-to-market. Medical Affairs has moved center stage and now plays a strategic role in launch preparations. To have faster drug and device launches with proven outcomes, DGE is hosting a two-day conference like no other! Join us October 20-21, 2022, for the Medical Strategy & Product Launch Readiness Summit, streaming online.

MSLs are vital to the success of drug and device development. As front-line customer facing scientific experts, MSLs must be fully prepared to educate and gather crucial insights from KOLs while providing scientific information and data throughout the product lifecycle

DGE’s 3rd  Next-Gen MSL Excellence Summit returns in-person to provide MSLs and field medical professionals with the tools and strategies essential to demonstrate value to stakeholders, dynamically engage thought leaders, and map out a path for career advancement.

DGE’s 6th Digital Strategy & Innovation for Medical Affairs Summit is the largest and most impactful industry event for transforming your medical affairs department into one that implements progressive policies and patient centricity.

A strong omnichannel marketing campaign allows pharma to reach the right people, in the right place, with the right message. By prioritizing promotional spending based on previous impact and consumer data, marketers can truly optimize their investment. But do you have the technology and data necessary to make your marketing as successful as it could be?
 

DGE’s Omnichannel Marketing Strategy Symposium provides you with the skills and strategies you need for orchestrating a personalized marketing approach that wins the competition for your customers’ attention!

The 3rd Human Factors Engineering & Usability Studies Congress is the proven industry-leading event specifically focused on the needs of medical device and combination product professionals responsible for avoiding use errors and medication errors while building a positive user experience. As your combination product matures, are you ready to address more involved questions of practical design, troubleshooting, and answering involved questions from regulators? This unique learning and networking forum will empower HF professionals to grow more confident in their skills, guide their teams toward the right insource/outsource decisions, and set new strategies for device software.

With more clinical trials switching to fully decentralized and hybrid models, the need for a collaborative information exchange is more important than ever. At the 7th Virtual Clinical Trials Conference, hear actual case studies from current decentralized trials and discuss the future state of clinical research from top industry experts at the forefront of clinical trial designs. Explore what is working successfully and what obstacles you can avoid in data compliance, regulatory compliance and novel submission methods.
https://informaconnect.com/medtech-summit-us/?vip_code=P22MTUSGHO
CONNECT WITH KEY BUYERS AT MEDTECH SUMMIT US 2022 IN CHICAGO Whether you’re increasing your company profile, launching a new product or focusing on new business development opportunities, collaborate with us to identify custom solutions to help you reach your goals.
 
December 6-8 , 2022 Please find your discount code and link below.

P22MTUSGHO

https://informaconnect.com/medtech-summit-us/?vip_code=P22MTUSGHO

Successful diversity and inclusion strategies have been correlated with greater company performance—it isn’t just good for society, it’s an essential business strategy. There has never been a more critical time than now for Pharma, Healthcare, and their allied industries to transform their company culture to be more diverse and inclusive. By putting a greater emphasis on diversity in the workplace and among your clinical trial participants, you can positively impact drug innovation and development, disease awareness, and clinical trial outcomes.
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