Medical Device Regulations
Articles & Whitepapers
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Why Sterile Packaging is Crucial for Medical Devices
Patients who need medical treatment often fear being exposed to harmful germs and unsanitary instruments. Just the thought of a healthcare provider using an unsterilized surgical device or needle is enough to make people feel queasy. As a result, patients find it reassuring to watch a clinician remove healthcare devices from sterile packaging before starting a procedure. Sterile packaging ...
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How Proper Packaging Improves the Shelf Life of Medical Devices
Medical devices are incredibly important in today’s world. They play a significant role in the treatment and prevention of various medical conditions. However, their effectiveness can be ...
News
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CELLINK Announces CELLINK Vivoink: Our First Medical-Grade Bioink
CELLINK, a global leader in bioprinting technologies, is proud to announce a pioneering innovation in the field of regenerative medicine and tissue engineering with the launch of CELLINK Vivoink, the first-ever medical-grade bioink specially ...
FDA Establishes New Medical Device Category: FDA Authorization Now Required to Market UV Robots to Healthcare Facilities
FARCO-PHARMA initiates sales in the U.S.
Is data drift an issue for medical AI models - and what can we do about it?
Portal Instruments appoints Dr. Veena Rao, PhD, as Chief Business Officer
Equipment & Solutions
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Showcase
Silver Alginate Dressings
Effective against bacteria such as E. Coli, Staphylococcus Aureus and Yeast (Candida Albicans). Our Silver Calcium Alginates fabric can be supplied in roll form, slit reels or cut pieces, packaged and sterile. various GSM available. High absorbency, High conformability, Antibacterial performance*, Strong dressing, Reduced fibre shed, various GSM and cut sizes available on request, Biodegradable ...
Upcoming Events
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Showcase
IVDR: our next Challenge?
In practice: The agenda will be built considering case studies and (project/regulatory) experience from the EBF community and presentations from a call for abstract (deadline for abstract submission: 15 March 2024). Meeting attendance will be limited to 60 delegates with a maximum of 3 delegates/company.