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Global Surgical Robotics Market Report 2021: Intuitive Surgical Dominated the Market by Holding 79.82% Market Share in 2020


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The global surgical robotics market is anticipated to grow with a robust CAGR of 10.2% during the forecast period, 2021-2031. The market for surgical robotics generated $5.46 billion in 2020, in terms of value and is estimated to reach $16.77 billion by 2031.
The global surgical robotics market is anticipated to witness tremendous growth over the forecast period primarily due to the increasing prevalence rate of chronic disorders, elevating global population coupled with the geriatric population, improving reimbursement policies, and public initiatives and funding to develop technologically advanced products. The market for surgical robotics (product type) is divided into three segments, namely, surgical systems, instruments & accessories, and services. ....

Laura Wood , Titan Medical Inc , Haptics Enabling Force Feedback , Vicarious Surgical Inc , Venus Concept Inc , Stryker Corporation , Medicaroid Corporation , Stereotaxis Inc , European Union , Surgical Inc , Meerecompany Inc , Zimmer Biomet Holdings Inc , Monteris Medical Corporation , Neocis Inc , Corin Group , Globus Medical Inc , Office Hours Call , Intuitive Surgical Inc , Biorobotics Corporation , Company Profiles , E St Office Hours Call , Curexo Inc , Asensus Surgical Inc , Virtual Incision Corporation , Medrobotics Corporation , Surgical Robotics Market ,

Global Healthtech CEO Connect: Software As A Medical Device In The U.S. And EU Recap | MoFo Life Sciences


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On Friday, March 26, 2021, over 180 attendees worldwide attended McKinsey & Company’s first Global HealthTech CEO Connect of 2021. The discussion focused on regulatory and legal considerations for software as a medical device (SaMD) in both the United States and Europe and specific use cases for digital therapeutics and other digital health products. Speakers included Morrison & Foerster partners Bethany Hills and Wolfgang Schönig as well as special guest Corey McCann, president and CEO of Pear Therapeutics, in a fireside chat at the end of the program. 
Globally, the convergence of software technology and life sciences creates a massive opportunity for growth, and the market for these products is growing exponentially. Both the U.S. Food and Drug Administration (FDA) and European regulators have focused on establishing a regulatory framework for oversight of SaMD. ....

United States , Corey Mccann , Morrison Foerster , Eu Commission , International Medical Device Regulators Forum , Health Schemes Di , European Union , Mofo Life Sciences , Mckinsey Company , European Court , German Federal Institute For Drugs , Digital Health Apps , Eligibility Of Digital Health Applications For Reimbursement , Drug Administration , European Commission , Medicare Coverage Of Innovative Technology , Clinical Decision Support Software Guidance , Certification Pilot Program , Mofo Life , Global Healthtech , Bethany Hills , Wolfgang Sch , Pear Therapeutics , Pre Certification Pilot Program , Medicare Coverage , Innovative Technology ,

FDAnews Announces Pharmaceutical Postmarket Surveillance: Latest Developments in the Era of COVID-19 Webinar March 18, 2021


FDAnews Announces Pharmaceutical Postmarket Surveillance: Latest Developments in the Era of COVID-19 Webinar March 18, 2021
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Is the pandemic making postmarket surveillance even more difficult? Two former FDAers explain how to comply. Register today.
WCG FDAnews
Pharmaceutical Postmarket Surveillance:
An FDAnews Webinar
Are you confident you’re compliant with current FDA postmarket adverse event reporting regulations? Postmarket surveillance can be difficult during the best of times. And in the COVID-19 era it’s become even more difficult.
Cynthia Schnedar, Executive Vice President of Regulatory Compliance at Greenleaf Health and former Director of the Office of Compliance for FDA’s Center for Drug Evaluation and Research (CDER) and Dawn Wynder, a Project Manager for FDAQRC and a former FDA Investigator, will ensure attendees understand how the FDA conducts its postmarket safety surveillance and what one must do to ensure postmarket ....

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