13 training found
ComplianceOnline Training
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Medical Devices
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Product Approval, Promotions & post marketing surveillance for Medical Device Companies - Best Selling Package Webinar
ComplianceOnline has created these courses individually through world renowned experts and combined them together to create a comprehensive training resource for companies to train their employees. You can store it as a library material and train all your employees in these compliance issues to get them ready to face any kind of compliance challenge and overcome it through expert advice and best ...
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EU Medical Device Regulations - Comprehensive Compliance Training Course
Medical devices cannot be shipped to Europe unless they are in full compliance with the European Medical Device Directive (MDD). The compliance requirements vary, depending on the classification of the device. It's not just the CE marking requirements that manufacturers and exporters have to worry about, but also the way the MDD is linked to the EU Clinical Trial Directive and ISO Certification on commercializing products. This pack of 5 best-selling ...
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Premarket Notification to Recalls - Comprehensive Medical Device Regulations Training Package
The following is a pack of 5 best-selling training CDs for regulatory professionals in the Medical Device industry. These courses provide information on how medical device companies can achieve compliance in the important stages of device development, marketing and maintenance. In today's complex regulatory environment, medical device manufacturers often find that the road to compliance can be filled with unseen perils that can lead to warning letters ...
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Medical Device Software Development & Management - Comprehensive Training Package (4 Courses)
This Medical Device Software Development & Management package training will have 4 courses which covers FDA's Medical Device Software Regulation, Medical Device Software Verification and Validation, IQ / OQ / PQ Approach and IEC ...
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Compliant Supply Chain & Manufacturing for Medical Devices - Comprehensive Training Package (5 Courses)
This comprehensive training package is aimed at helping medical device companies ensure that their supply chain controls and manufacturing processes comply with existing regulations. This comprehensive training package is aimed at helping medical device companies ensure that their As manufacturing becomes increasingly global, with responsibility for various parts of the final product vesting with multiple parties, regulatory compliance can be ...
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Validation for FDA and ISO 13485 Compliance: Pack of Two Courses
Computer system validation and risk-based verification and validation planning to meet US FDA and ISO 13485 ...
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Best Selling Medical Devices webinars
This pack of 4 courses contains some of our best selling Medical Device webinars which together cover the essential compliance challenges faced by Medical Device companies ...Pack of two courses: The essentials of Food and Drug Administration Medical Device Regulations: A primer for manufacturers and suppliers
This pack of 2 courses contains the essentials of FDA Medical Device regulations. In the United States, the US Food and Drug Administrates Medical Devices through several different regulations, the principle one is the Quality System Regulation 21 CFR 820 (QSR). Other regulations include Registration and Listing, Labeling, Medical Device Reporting, and Corrections and Removals (Recalls). This 3-hour course pack will give an overview of all the major ...
FDA Compliant Marketing/Promotions for Medical Device Companies - Best Selling Package Webinar
The following is a pack of 4 best-selling training CDs for sales, marketing & regulatory professionals in the Medical Device industry. These courses provide solutions for all critical challenges & questions faced by you and your team pertaining to regulations/compliance, best practices, etc. ComplianceOnline has created these courses individually through world renowned experts and combined them together to create a comprehensive training ...
EU Medical Device Regulations - Comprehensive Compliance Training Course
The following is a pack of 3 best-selling training CDs for regulatory professionals in the Medical Device industry. These courses provide information on how medical device companies can achieve compliance with the EU Medical Device Directive, obtain CE marking and fulfill ISO ...From Premarket Notification to Recalls - Comprehensive Medical Device Regulations Training Package
The following is a pack of 8 best-selling training CDs for regulatory professionals in the Medical Device industry. These courses provide information on how medical device companies can achieve compliance in the important stages of device development, marketing and ...
Medical Device Software Development & Management - Comprehensive Training Package (4 Courses)
This medical device software development, verification and validation training package of four courses covers wellIEC 62304 requirements and explains risk based approach for validation using validation protocols and GAMP®. Medical device software can make or break a device. Badly developed, non-compliant software can compromise a device's safety and reliability. These four webinar recording CDs cover not just the IEC 62304 requirements for medical ...
Compliant Supply Chain & Manufacturing for Medical Devices - Comprehensive Training Package (8 Courses)
This comprehensive training package of 8 courses is aimed at helping medical device companies ensure that their supply chain controls and manufacturing processes comply with existing ...