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Medical Product Training Courses Available In In Asia Middle East
9 training items found
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 ...
Manufactured by:Tulip Medical Products based inSan Diego, CALIFORNIA (USA)
Tulip team members are available to demonstrate products and to train you and your staff in the use of the Tulip Master Collections for new patient applications such as Tulip TRUE NanoFat™ for under-eye discoloration, scar revision, and non-surgical facial tightening and brightening. ...
Manufactured by:Tecme based inAgustín Tosco, 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 ...
Manufactured by:TSK Group based inVancouver, BRITISH COLUMBIA (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 ...
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)
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)
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 ...
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 the way the MDD is linked to the EU Clinical Trial ...