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Medic First Aid Cpr Training Training Courses In Usa California
13 training items found
by:Safety Unlimited, Inc. based inSimi Valley, CALIFORNIA (USA)
Nationally Registered EMRs (NREMR) are required to renew their certification every two years. NREMRs can recertify by either taking the cognitive examination or by completing continuing education. Our 16 Hour (F5) NCCP EMR Refresher provides all the continuing education needed for those currently certified by NREMT. We encourage you to reference the specific license renewal requirements for every ...
by:TeraRecon, Inc. based inDurham, NORTH CAROLINA (USA)
Train your entire team! Our classes are designed to foster efficient use of our products and are tailored toward specific roles within your organization. Classes are available for clinicians, technicians, super-users, referring physicians, and system administrators. ...
Manufactured by:ICU Medical, Inc. based inSan Clemente, CALIFORNIA (USA)
Smiths Medical is committed to advancing knowledge and improving care by providing education on clinical solutions, product training courses, and professional continuing education programs. The Smiths Medical Online Training Portal offers self-paced learning for healthcare ...
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:IMSM Ltd based inMalmesbury, UNITED KINGDOM
ISO 13485 specifies requirements for a Quality Management System for organisations required to demonstrate its ability to provide medical devices that consistently meet client and regulatory ...
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 integrated into ...
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 environment, medical device manufacturers often find that the road to compliance can be ...
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, with responsibility for various parts of the final product vesting with ...
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)
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 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)
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 ...
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 ...