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ISO 13485
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#	Item
51	Rocky Mountain Regulatory Affairs Society presents Quality System Regulation Course Friday, May 15, 2015 8:00 am – 5:00 pm First created by RMRAS in 1997, this is the must-attend course for all personnel working in qua Add to Reading List Source URL: rmras.org Language: English - Date: 2015-05-26 17:27:21 Medical equipment Medical technology Quality management Auditing ISO 13485 Food and Drug Administration Regulatory affairs Quality management system Quality audit Medicine Technology Health
52	Medical technology Innovation for success – Customized solutions in medical technology Innovation for success Add to Reading List Source URL: www.cicor.com Language: English - Date: 2014-07-29 12:20:37 Quality management Medical device ISO 13485 Quality management system Traceability Quality assurance Reliability engineering Technology Medical equipment Medical technology
53	Monday, March 16, 2015 3:30 pm – 4:00 pm Registration and Networking 4:00 pm – 5:00 pm Add to Reading List Source URL: rmras.org Language: English - Date: 2015-05-26 17:27:21 Medical equipment Actuarial science Risk management ISO 14971 ISO 13485 Medical device Risk PM Denver Medicine Technology Medical technology
54	Job Title: Regulatory Affairs Specialist Location: Add to Reading List Source URL: www.acornregulatory.com Language: English - Date: 2015-04-23 10:35:15 Health Medical technology Pharmaceuticals policy Quality management ISO 13485 Global Harmonization Task Force Regulatory affairs Medical device Regulatory requirement Medicine Technology Medical equipment
55	Questionnaire for the Preparation of a Quotation Details of the Company Main site (address for the certificate) Company (Name and Legal Entity) Street Postal Code, Place Add to Reading List Source URL: www.mdc-ce.de Language: English - Date: 2015-05-29 10:56:30 Medical equipment Medical device Quality management ISO 13485 Medical Devices Directive Sterilization Quality management system Medicine Technology Medical technology
56	Antworten und Beschlüsse des EK-Med Konformitätsbewertung 3.9 B 20 Add to Reading List Source URL: www.mdc-ce.de Language: English - Date: 2013-10-31 06:25:43 Medical technology CE mark European Economic Area Medical device Notified Body Public key certificate Type approval Medical Devices Directive ISO 13485 Technology Product certification Medical equipment
57	Job Title: Regulatory Affairs Specialist Location: Add to Reading List Source URL: www.acornregulatory.com Language: English - Date: 2015-04-24 06:23:23 Health Medical technology Pharmaceuticals policy Quality management ISO 13485 Global Harmonization Task Force Regulatory affairs Medical device Regulatory requirement Medicine Technology Medical equipment
58	Press Release December 17th 2012 HEALTH \| INNOVATION \| FLUORESCENCE IMAGING \| REGULATORY APPROVAL Fluoptics announces the CE marking of its Fluobeam® system The Grenoble based start-up has also obtained the quality cert Add to Reading List Source URL: fluoptics.com Language: English - Date: 2014-03-19 03:50:12 Medical technology Health ISO 13485 CE mark Minatec Medicine Technology Medical equipment
59	Certificate of Registration QUALITY MANAGEMENT SYSTEM - ISO 13485:2003 This is to certify that: Oberg Costa Rica Ltda. Zona Franca Metropolitana Add to Reading List Source URL: www.oberg.com Language: English - Date: 2014-11-06 12:02:21 BSI Evaluation United Kingdom Reference British Standards IEC BSI Group
60	Certificate of Registration QUALITY MANAGEMENT SYSTEM - ISO 13485: 2003 This is to certify that: Weaver and Company 565 Nucla Way, Unit B Add to Reading List Source URL: www.weaverandcompany.com Language: English - Date: 2013-12-12 13:22:21 Public-key cryptography BSI Film speed Public key certificate Evaluation Reference United Kingdom British Standards IEC BSI Group