Medical Device Training Courses Available In In Iran
30 training items found
by:NetZealous LLC based inFremont, CALIFORNIA (USA)
Having started out as a training provider for this segment; NetZealous has accumulated total knowledge of the medical devices industry. With its long experience and in having several leading names in the medical devices industry on its panel, NetZealous covers all areas of medical devices ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
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 ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
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 ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
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 ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
This comprehensive training package of ten courses is aimed at helping medical device companies gain a thorough understanding of the top 10 regulations that they should comply ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
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 ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
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 ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
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 ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
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 ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
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, ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
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 ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
Conducting clinical trials in a rapidly evolving electronic environment presents a unique challenge to the medical device industry where not only quality (GLP/GMP) plays an essential role – but collecting accurate, maintaining viable data (GCP) as part of continuous process improvement (while mitigating risk) is an essential and critical component of the ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
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 ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
This Water system compliance training will give you a comprehensive knowledge about water system compliance with relation to Microbial Quality Problems, Microbial Testing, Endotoxin control, Sanitization, Water system validation. Water can be a major source of microbial contamination in the manufacturing systems for Medical Devices, Diagnostics, Pharmaceuticals, ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
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 ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
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, ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
Many regulated companies have not brought their old products up to current FDA standards and are not in total compliance. This webinar defines the criteria to be used for medical products design history file remediation. For example companies should be compliant to 14971:2007. Design History Files need to be updated to meet current standards. The FDA expects risk management to be ...
Manufactured by:Winncare Group based inPresteigne, UNITED KINGDOM
The 2007-47 European Directive amended Directive 93-42 by introducing 2 new important concepts for medical devices (MD): the medical device user profile, the user environment for the aforesaid ...
Manufactured by:Sisu Global Health based inBaltimore, MARYLAND (USA)
During this training you will gather knowledge about Heamfuse as a product as well as been given the tools for Sales Learning and Common Objections in the medical device Sales Field. ...
by:NetZealous LLC based inFremont, CALIFORNIA (USA)
Surgical instruments, given the nature of their use, are extremely important devices of the medical industry. That they come with the highest and most stringent quality standards goes without saying. Our in-depth experience in the medical devices industry makes us the ideal provider of trainings on any aspect of surgical ...