What Industry Is Saying About Proposed Ethylene Oxide Sterilization Ban By MedTech Intelligence Staff Stakeholders warn that more EtO facility closures could have a catastrophic result. |
Featured Articles |
Quality and Software Issues Remain Top Reasons for Medical Device Recalls By MedTech Intelligence Staff The number of recalls also increased 21.5% this quarter, according to Stericycle’s Q3 2019 Recall Index. |
Top 3 Mistakes You Can Make When Adopting ISO 13485 By Jon Speer, GreenlightGuru Drop the checkbox mentality and embrace accountability and understanding. |
Ameing for Asia Asian Giants Gain Medical Robotics Foothold By Ames Gross, Pacific Bridge Medical Across the continent, governments and hospitals are purchasing robotics systems from abroad as well as developing the technologies themselves. |
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Featured Quote — Kumar Sharma, M.D., UT Health San Antonio |
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By Messe Düsseldorf The transition to digital in healthcare is happening at a fast pace. |
MEDICA 2019 Trends: By Dr. Lutz Retzlaff, Contributing Writer Topics from regenerative medicine to artificial intelligence to cannabis will be discussed. |
MedTech Deals Worth $15.8 Billion in Q2 By MedTech Intelligence Staff With 253 deals occurring during this year’s second quarter, the medical device industry experienced an 11% increase in deal activity versus its four-quarter average. |
Resource Centers |
Resource Centers are single topic focused micro-sites within MedTechIntelligence.com that are portals of information on medical device components and quality systems offering news, articles, white papers, case histories and videos. |
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Sponsored Resources |
EU MDR: REQUIREMENTS & IMPLEMENTATION THIS EVENT WAS RECORDED JULY 17, 2019 | On Demand Webcast This on-demand recording of the four-hour virtual event that took place July 17, 2019, conducted by leading experts on EU MDR requirements and implementation, provides concise insights into key aspects of the regulation to help companies understand and plan for the impending changes. The four hour webcast recording is $495.00 |
ADVANCED CAPA & ROOT CAUSE ANALYSIS THIS EVENT WAS RECORDED MARCH 26-27, 2019 CAPA is the most critical and challenging quality system requirement in terms of complex thinking and organizational processes. How do you verify effectiveness? How can you apply project management to CAPA? What are the right data and tools for identifying trends? How do you deal with significant but infrequent problems? Should you set deadlines for closing CAPAs, and what about CAPAs that never close? What are best practices for documenting and communicating CAPA results? Not a CAPA 101 course, this workshop recording brings together leading industry CAPA process owners to discuss approaches to the most difficult problems in CAPA and root cause analysis. |
Upcoming Events & Webinars |
February 4-6, 2020 - EU MDR Implementation Strategies |
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