Medical Products Training For Medical Equipment
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based in 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 ...
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based in USA
Medical device manufacturing is one of the most regulated sectors in which significant quality systems and product requirements must be satisfied. The regulatory requirements are intended to ensure that manufacturers consistently design, produce and place onto the market medical devices that are safe and fit for their intended purpose. The ISO 13485 standard is an effective solution to meet the ...
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based in 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 ...
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Manufactured by Tecmebased in ARGENTINA
Our progress is possible thanks to the joint work and commitment of professionals willing to share their knowledge and experience in order to train distributors and medical professionals. These training programs are backed by the highest quality standards, in order to guarantee the efficient and safe implementation of our ...
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Manufactured by Novair Medicalbased in FRANCE
Since 1977, NOVAIR designs, manufactures and markets solutions of production and distribution of medical gases. Today, we share our expertise via the development of training sessions dedicated to technical & biomedical services, as well as healthcare facility services in charge of the distribution and maintenance of medical gases supply systems. The program of those training sessions can be ...
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based in 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 ...
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based in USA
The following is a pack of 4 best-selling training CDs for sales, marketing & regulatory professionals in the Pharmaceutical 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 ...
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Manufactured by TSK Groupbased in CANADA
TSK aesthetic training partners offer aesthetic courses for all experience levels. TSK Laboratory offers you a unique opportunity to attend a highly-specialised medical aesthetic masterclasses led by multi-award-winning tutors and key opinion leaders. In these aesthetic training courses, elite tutors will share their in-depth knowledge and experience through one to one guidance and detailed ...
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based in 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 the way the MDD is linked to the EU Clinical Trial Directive and ISO Certification ...
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based in 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 ...
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based in USA
BSI's “Medical Devices CE Marking” three day course is designed to provide participants with the knowledge to assist their companies in getting products to market more quickly. Management personnel responsible for all aspects of CE marking medical devices as well as internal and external auditors will benefit from this course. Participants will gain knowledge of the requirements of ...
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