Explore the digital transformation of healthcare and how #MedTech companies are prioritizing digital engagement in #omnichannel strategies in order to achieve adoption, growth, and loyalty for their #medicaldevice or diagnostic. https://bit.ly/4d1ugnf Michaela Miller Nicola Partridge MSc
IQVIA MedTech
Medical Equipment Manufacturing
Global Partner for accelerating MedTech innovation
About us
IQVIA MedTech, part of IQVIA, is a global strategic partner for accelerating MedTech innovation. Leveraging our global presence and local expertise, IQVIA MedTech intelligently connects the right insights, streamlined technology and deep MedTech expertise to help enhance healthcare outcomes of the medical device and in vitro diagnostics industry. Our market leading and specialized solutions and services help boost product strategy with advanced data driven insights, optimize clinical success with accelerated trials and real-world evidence, streamline efficient pathways for regulatory approvals, ensure compliance with comprehensive cloud-based solutions and field recall, and maximize business performance with augmented team solutions along the complete product lifecycle. Learn more at iqviamedtech.com IQVIA (NYSE:IQV) is a leading global provider of information, innovative technology solutions, and contract research services.
- Website
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http://iqviamedtech.com
External link for IQVIA MedTech
- Industry
- Medical Equipment Manufacturing
- Company size
- 10,001+ employees
- Headquarters
- New York
- Founded
- 2016
- Specialties
- Medical Devices and Diagnostics, MedTech, IVD, Commercial, Full clinical Trials, Legal/Compliance/Risk Management, Recall, Global Data and Analytics, Consulting, Primary Market Research, Quality Management, Master Data Management, Regulatory Strategy, Consulting, Management, and Outsourcing (Technical, Clinical, Sales, Field, Inside Sales)
Updates
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As the MedTech industry is undergoing rapid change, IQVIA MedTech can help you to successfully navigate these evolving market dynamics. Check out our dedicated web page to learn more about our comprehensive solutions, and access our podcast series, full of insightful discussion with MedTech industry experts. https://bit.ly/3VZrYhw #MedTech #MarketDynamics
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Real World Data (RWD) can enhance the safety and effectiveness of medical devices, but the quality controls differ from those of traditional clinical studies. In our on-demand webinar, we delve into the specifics of the recently released FDA draft guidance that provides considerations for evaluating the relevance and reliability of RWD for regulatory decision-making. Watch now. https://bit.ly/4eVZrlv #RWD #MedicalDevices
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What do you do when you have 90 days to carry out a class II field action, no field presence, and you need a speciality skillset to get the job done? Don’t leave it to chance: make sure you’re always recall ready with IQVIA MedTech. Find out more. https://bit.ly/45Xux86 #MedicalDevice #Recall
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Looking to overcome challenges in validating and evaluating the safety of innovative medical technologies? See how IQVIA #MedTech leveraged the IQVIA Research Management platform to help a sponsor validate their investigational product for clinical use: https://bit.ly/4bRlbMR
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Many factors can slow down the adoption of your #medicaldevice — from lack of investment to low case volumes. Find out why it's important to understand healthcare systems and discover a real-life example of #MedTech adoption differences across countries: https://bit.ly/3XVyzMh
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Modernize your #MedTech marketing and transform digital multi-channel #customerengagement with an innovative solution from #IQVIA's Digital Enablement Center of Excellence that delivers personalized content to fit your #omnichannel marketing goals. https://bit.ly/3WdckiL
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As MedTech stocks continue to feel pressure from GLP-1 drugs for obesity, MedTech companies are increasingly tasked with articulating the value of their products. In our latest blog, IQVIA MedTech discusses current market shifts, and explains how IQVIA can offer crucial insights into the dynamics of GLP-1 markets and patient profiles at a global, national, and regional level. Read now. https://bit.ly/3LaJMkE #GLP1 #MedTech Authors: Christopher Ludwig and Michelle Edwards
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As manufacturers strive to meet new requirements in transitioning from the In Vitro Diagnostic Directive (IVDD) to IVDR, we provide critical insight to help you navigate the complexity of IVD regulations. Download our latest Insight Brief now. https://bit.ly/3VSbJCJ #IVDRTransition #IVDRegulations #MedicalDevices
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Only a few European countries are sufficiently advanced in their reimbursement policies for SaMD. In the third instalment of our ‘Reimbursement of SaMD in Europe’ series, IQVIA MedTech’s Dr. Aleksandar Petrović discusses pioneering countries with systematic pathways for reimbursement of digital health solutions, and considers national initiatives in leading countries such as France and the UK. Read now. https://bit.ly/45SnDkP #SaMD #MedicalDevices
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