I just entered Yoga Society's Giveaway to win a $50 Gift Card and a 4-pack of Face Masks! Help us both out by entering through this link. You get a bonus entry and I get 3 bonus entries! Hurry, giveaway ends soon. https://t.co/R7d1R3yS41 via @yogasociety_
When product development teams engage subject matter experts, it’s best to do so early and often. Get more insight on product development and regulatory from Kapstone Medical's CEO, John Kapitan at https://t.co/Emrv6JNmwC @OMTEC_BONEZONE#medicaldevices#regulatory
"Conduct research to find specific, appropriate information in regards to regulations that will impact your specific design." Get tips on keeping up with regulatory requirements from John Kapitan, CEO, Kapstone Medical. https://t.co/Emrv6JNmwC @omtec_bonezone#productdevelopment
"New regulations don’t always have to cause massive production delays." Learn more about keeping up with increased regulatory requirements from John Kapitan, CEO, Kapstone Medical. https://t.co/Emrv6JNmwC @omtec_bonezone#productdevelopment#regulatory#medicaldevices
With the new MDR, the redesigned European Database for Medical Devices (EUDAMED) system is expected to go live in March 2020. Find out what the new system will consist of at - https://t.co/PNDJ4NaaST. #MDR#EUMDR#medicaldevices
With the new MDR, EU commission recognized that it would need to greatly expand the capabilities of the European Database for Medical Devices (EUDAMED) for monitoring and data collection. Discover more at - https://t.co/PNDJ4NrLKr. #MDR#EUMDR#medicaldevices
The MDR states that “Manufacturers should play an active role during the post-market phase..." Find out what this means for device makers at https://t.co/frallboIeu. #MDR#EUMDR#medicaldevices
The new MDR was specifically updated to ensure that manufacturers do not passively wait for information to come to them. Discover more at https://t.co/frallboIeu. #MDR#EUMDR#medicaldevices
Are you ready to go further with your medical device idea? Find out how we can guide you through the new product development process at https://t.co/oFaSQMLAZ8. #productdevelopment#innovation#medicaldevices
It's time to remove all risks in your investment and take the necessary steps to successfully sell a safe medical device. Visit https://t.co/oFaSQMLAZ8 for more information. #productdevelopment#innovation#medicaldevices
Under clinical requirements, the new regulation requires clinical evaluation including the collection of clinical data readily available in the literature as well as ongoing clinical investigations. Find out more at https://t.co/3JB3HyE7BG. #medicaldevices#MDR#EUMDR
Minimize risks in your next medical device project with our five-phased new product development (NPD) process. Find out more at https://t.co/bOfVExWEDG. #productdevelopment#innovation#medicaldevices
The new Medical Devices Regulation (MDR) imposes a number of obligations on manufacturers. Here's what you need to know - https://t.co/3JB3HyE7BG. #medicaldevices#MDR#EUMDR
Under the EU's Medical Device Regulation, device makers face significant changes around clinical evidence requirements. Here's what you need to know - https://t.co/COVFbNIhjm. #MDR#EUMDR#medicaldevices
A taxing effort for companies that already have CE-marked devices in the EU is the need for portfolio reviews. Here are some key points about the importance of reviewing your product portfolio & technical documentation - https://t.co/MQf7qHMJoX. #EUMDR#MDR#medicaldevices