Happy Monday 6/12/23
Cloud Staffing Professionals would like to wish everyone a wonderful start to the work week! As you can see from our videos we are working tirelessly to ensure only the best quality on our end! Our staff does a wonderful job every week and should be commended for such. If you’re currently looking for your […]
New Design – 6/9/23
Hello, thank you for coming to the Website for Cloud Staffing Professionals! A veteran owned Life Sciences and Engineering company! We are pleased to announce that due to popular demand we are increasing our offerings to the IT industry! Our senior staff has inroads with many consultants and clients that have asked us on a […]
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December 9, 2019 – Global Regulatory Update
Saudi Arabia Saudi Arabia’s Saudi Food and Drug Authority (SFDA) has rolled out a single registration platform for all medical device market authorization, authorized representation, and related applications to be submitted to the regulator. The new system, Ghad, provides a single platform for submitting Medical Device Marketing Authorization (MDMA), Medical Device National Registry (MDNR), Saudi […]
Post-Market Surveillance
Medical device post-market surveillance (PMS) activities are described in the European Medical Device Directive (93/42/EEC) and are part of the Quality Management System (QMS) certification under EN ISO 13485:2016. However, resulting from various concerns surrounding PIP implants, PMS activities and oversight powers of Notified Bodies (NB) and Competent Authorities (CA) have been reinforced. Therefore, consequently, […]
FDA Guidance Documents
The US FDA has produced the A-List of Guidance Documents that CDRH intends to publish in FY2020. A-List: Prioritized Guidance Documents for FY2020 Final Guidance Topics Select Updates for Recommendations for Clinical Laboratory Improvement Amendments of 1988 (CLIA) Waiver Applications for Manufacturers of In Vitro Diagnostic Devices Recommendations for Dual 510(k) and Clinical Laboratory Improvement […]
