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SGB Qa/Ra Consulting LTD
sgb qa/ra consulting was launched in 2017 to provide a complete range of services to meet the qa/ra compliance needs of medical device companies. we have over 25 years’ experience working with a range of medical device clients from start-ups to global multi-nationals on a wide range of projects including: mdd to mdr upgrade ivdd to ivdr upgrade iso 13485:2016 ce marking audit remediation market access: 510k submissions / mdsap / asean / canada / australia brexit preparation - eu authorised representative / uk responsible person internal auditing (iso 13485, iso 27001) fda warning letters / remediation software as a medical device (samd) digital health & cybersecurity udi (unique device identification) outsourced monthly qa/ra support bespoke remote / onsite client training
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Distrobird — Free Sales Engagement Platform
Sequences, cloud call center, shared inbox, form tracking and more — on a single platform. Double your sales team's output with fewer tools.
Create a sequence — it's free