{"id":236,"date":"2015-03-04T19:54:07","date_gmt":"2015-03-04T19:54:07","guid":{"rendered":"https:\/\/compliancems.com.au\/?p=236"},"modified":"2015-03-04T19:54:07","modified_gmt":"2015-03-04T19:54:07","slug":"australian-tga-medical-device-conformity-assessment","status":"publish","type":"post","link":"https:\/\/compliancems.com.au\/?p=236","title":{"rendered":"Australian TGA Medical Device Conformity Assessment"},"content":{"rendered":"<p><span style=\"color: #000000; font-family: Calibri; font-size: medium;\">As of recent, the TGA was the only Notified Body that can issue Conformity Assessments (CA) for Australian medical device manufacturers (intended to be sold in Australia). <\/span><br \/>\n<span style=\"font-family: Calibri;\"><span style=\"font-size: medium;\"><span style=\"color: #000000;\"> Finally, there has been a paradigm shift whereby the TGA will now accept conformity assessments from 3rd party Notified Bodies &#8211; what the Australian medical device industry has been pushing for for quite some time now has finally come to fruition.<\/p>\n<p>This means that Australian MD manufacturers will no longer require TGA Conformity Assessment to manufacture and sell medical devices here in Australia; European EC Certificates will now be accepted (class dependant).<\/p>\n<p>For more information on this regulatory change contact Compliance Management Solutions.<\/p>\n<p><\/span>About CMS: <\/span><\/span><\/p>\n<p><span style=\"color: #000000; font-family: Calibri; font-size: medium;\"> Compliance Management Solutions is an Australian based consultancy assisting organizations in TGA\/MDD | ISO 9001 (Quality) | 13485 (Medical Devices) | Cosmetics GMP ISO 22716 certification, registration and consultation. Our services include: <\/span><\/p>\n<p><span style=\"font-size: medium;\"><span style=\"font-family: Symbol;\">\u00d8<\/span><span style=\"font-family: Calibri;\"> Australian ARTG registration\/sponsorship\/consultancy (medical devices\/medicinal products) <\/span><\/span><br \/>\n<span style=\"font-size: medium;\"><span style=\"font-family: Symbol;\">\u00d8<\/span><span style=\"font-family: Calibri;\"> Implementation and maintenance of Management Systems (MDD\/ISO 13485\/Sterilization\/ISO 9001) <\/span><\/span><br \/>\n<span style=\"font-size: medium;\"><span style=\"font-family: Symbol;\">\u00d8<\/span><span style=\"font-family: Calibri;\"> Management Systems audits \u2013 (MDD\/ISO 13485\/Sterilization\/ISO 9001) <\/span><\/span><br \/>\n<span style=\"font-size: medium;\"><span style=\"font-family: Symbol;\">\u00d8<\/span><span style=\"font-family: Calibri;\"> 3rd Party Notified Body Certification Audits (MDD\/ISO 13485\/ISO 9001\/ISO 22716) <\/span><\/span><br \/>\n<span style=\"font-size: medium;\"><span style=\"font-family: Symbol;\">\u00d8<\/span><span style=\"font-family: Calibri;\"> Quotations for ISO transfer of certificate <\/span><\/span><br \/>\n<span style=\"font-size: medium;\"><span style=\"font-family: Symbol;\">\u00d8<\/span><span style=\"font-family: Calibri;\"> Risk Management <\/span><\/span><br \/>\n<span style=\"font-size: medium;\"><span style=\"font-family: Symbol;\">\u00d8<\/span><span style=\"font-family: Calibri;\"> Continuous improvement including Corrective\/Preventive Action <\/span><\/span><br \/>\n<span style=\"font-size: medium;\"><span style=\"font-family: Symbol;\">\u00d8<\/span><span style=\"font-family: Calibri;\"> Validation including (Process\/Equipment Qualification\/Sterilization) <\/span><\/span><br \/>\n<span style=\"font-size: medium;\"><span style=\"font-family: Symbol;\">\u00d8<\/span><span style=\"font-family: Calibri;\"> Machinery\/Equipment commissioning\/installation and troubleshooting <\/span><\/span><br \/>\n<span style=\"font-size: medium;\"><span style=\"font-family: Symbol;\">\u00d8<\/span><span style=\"font-family: Calibri;\"> Complaint handling <\/span><\/span><br \/>\n<span style=\"font-size: medium;\"><span style=\"font-family: Symbol;\">\u00d8<\/span><span style=\"font-family: Calibri;\"> Process Improvement using Lean Six Sigma methodologies <\/span><\/span><br \/>\n<span style=\"font-size: medium;\"><span style=\"font-family: Symbol;\">\u00d8<\/span><span style=\"font-family: Calibri;\"> Web based compliance management software <\/span><\/span><br \/>\n<span style=\"color: #000000; font-family: Calibri; font-size: medium;\"><br \/>\nCompliance Management Solutions<br \/>\nMelbourne, Australia<\/p>\n<p>E: gloizou@compliancems.com.au | M: 0433 12 42 66<br \/>\nW: <a href=\"https:\/\/compliancems.com.au\">www.compliancems.com.au<\/a><\/span><\/p>\n","protected":false},"excerpt":{"rendered":"<p>As of recent, the TGA was the only Notified Body that can issue Conformity Assessments (CA) for Australian medical device manufacturers (intended to be sold in Australia). Finally, there has been a paradigm shift whereby the TGA will now accept conformity assessments from 3rd party Notified Bodies &#8211; what the Australian medical device industry has been pushing for for quite some time now has finally come to fruition. This means that Australian MD manufacturers will no longer require TGA Conformity Assessment to manufacture and sell medical devices here in Australia; European EC Certificates will now be accepted (class dependant). For more information on this regulatory change contact Compliance Management Solutions.[&#8230;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[],"class_list":["post-236","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"_links":{"self":[{"href":"https:\/\/compliancems.com.au\/index.php?rest_route=\/wp\/v2\/posts\/236","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/compliancems.com.au\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/compliancems.com.au\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/compliancems.com.au\/index.php?rest_route=\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/compliancems.com.au\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=236"}],"version-history":[{"count":2,"href":"https:\/\/compliancems.com.au\/index.php?rest_route=\/wp\/v2\/posts\/236\/revisions"}],"predecessor-version":[{"id":238,"href":"https:\/\/compliancems.com.au\/index.php?rest_route=\/wp\/v2\/posts\/236\/revisions\/238"}],"wp:attachment":[{"href":"https:\/\/compliancems.com.au\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=236"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/compliancems.com.au\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=236"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/compliancems.com.au\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=236"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}