๐๐ง๐ญ๐ซ๐จ๐๐ฎ๐๐ข๐ง๐ ๐๐ฎ๐ซ ๐๐๐ฐ ๐๐จ๐ฌ๐ญ-๐๐๐ซ๐ค๐๐ญ ๐๐ฎ๐ซ๐ฏ๐๐ข๐ฅ๐ฅ๐๐ง๐๐ (๐๐๐) ๐๐๐ฉ๐จ๐ซ๐ญ๐ข๐ง๐ ๐๐ฎ๐ฉ๐ฉ๐จ๐ซ๐ญ ๐๐๐ซ๐ฏ๐ข๐๐
International Associates Limited is excited to announce our latest offering: Post-Market Surveillance (PMS) Reports. Ensuring compliance with ISO 13485:2016 and regulatory requirements such as UK MDR, EU MDR, and FDA QSR has never been easier.
๐๐ก๐ฒ ๐ข๐ฌ ๐๐๐ ๐ข๐ฆ๐ฉ๐จ๐ซ๐ญ๐๐ง๐ญ?
๐๐๐ ๐ฎ๐ฅ๐๐ญ๐จ๐ซ๐ฒ ๐๐จ๐ฆ๐ฉ๐ฅ๐ข๐๐ง๐๐: All medical devices must have a PMS plan, and regular PMS reports are crucial for maintaining compliance.
๐๐จ๐ฆ๐ฉ๐ซ๐๐ก๐๐ง๐ฌ๐ข๐ฏ๐ ๐๐ง๐ฉ๐ฎ๐ญ: Our PMS reports consider Field Safety Notices (FSNs), Field Safety Corrective Actions (FSCAs), new clinical literature, material reports, and safety bulletins.
๐๐จ๐ฐ ๐๐๐ง ๐ฐ๐ ๐ก๐๐ฅ๐ฉ ๐ฒ๐จ๐ฎ?
๐๐ฎ๐ฌ๐ญ๐จ๐ฆ ๐๐๐ ๐๐ฅ๐๐ง๐ฌ: Donโt have a PMS plan? We can create one tailored to your needs.
๐๐๐ญ๐๐ข๐ฅ๐๐ ๐๐๐ฉ๐จ๐ซ๐ญ๐ฌ: Provide us with your device details, and we’ll compile a comprehensive PMS report for you.
Ensure your devices meet all necessary standards with our expert support. Contact us today to discuss.
enquiry@ia-uk.com | www.ia-uk.com
Effortless and Effective PMS Reporting Solutions
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