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Medical Flow Selector Device Training Courses Near Canada Quebec
40 training items found
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:Marcus Evans based inLondon, UNITED KINGDOM
Mastering all aspects of present-day marketing through highly practical workshops with real life examples and discussions with like-minded professionals. This series includes spin-off programmes tailored to help maintain a competitive edge whilst boosting success in the market. Selection of courses relevant for all marketing practitioners’ levels focusing on Marketing, Marketing ...
by:Kelmac Group based inLimerick, IRELAND
This course aims to provide learners who have an existing, basic knowledge of, or experience in, quality management in the Medical Device Industry and in the context of the requirements of ISO 13485, compatible with ...
by:Korea Testing & Research Institute (KTR) based inGwacheon, SOUTH KOREA
KTR operates a separate website (www.ktr.or.kr/edu) that provides education/training related tasks including introduction of training programs, applications for training, and education/training history ...
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 ...
by:Apex Quality Assurance based inHampstead, NORTH CAROLINA (USA)
Although the ISO 9001 requirements have been removed from IATF 16949:2016 and are published as a separate ISO standard, IATF 16949 is not a stand-alone standard and must be used in conjunction with ISO 9001, we offer courses that cover both the ISO 9001:2015 and IATF 16949:2016 requirements. Group exercises and case studies with examples from the automotive industry will be used to develop the ...
by:Smithers based inAkron, OHIO (USA)
This Course is provided to give product designers and developers an understanding of the underlying principles of medical device regulations and their requirements for medical device design and to then apply these requirements when identifying plastics materials that are suitable for use with medical devices. A detailed over view of the EU Medical Device Directive 93/42/EEC is given and the ...
by:Fizimed SAS based inStrasbourg, FRANCE
We place the utmost importance in our work with health care professionals. The Emy biofeedback Kegel trainer allows the patients you treat in your practice during pelvic floor therapy to continue their pelvic floor exercises at home. Discover our solutions that facilitate both your work and the daily lives of ...
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:Quality Management International, Inc. (QMII) based inAshburn, VIRGINIA (USA)
When medical device nonconformities occur, peoples' lives are often at stake. Consequently, the medical device industry is one of the most heavily regulated, and product and process compliance is a primary objective for all quality management systems for medical ...
Manufactured by:AbClo Medical based inMarkham, ONTARIO (CANADA)
The AbClo education course offers an in-depth understanding of the fundamentals and applications of AbClo in the healthcare industry. Designed for users at all levels, this one-week course includes 34 lessons and 2 quizzes to clarify AbClo's role in optimizing care delivery. By examining why and how AbClo functions, participants can recognize its potential to bridge existing healthcare gaps. ...
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 instruments, which are a part of the medical device industry. Like all our ...
by:EuroQuest based inAtlanta, GEORGIA (US) (USA)
This three-day program is designed for quality professionals with a knowledge of medical device manufacturing. The objective of the course is to teach, through lectures, workshops and exercises, how to plan, conduct and report internal audits that are compliant for the medical device industry. In so doing participants will review the new 2003 standard from an auditor’s perspective, ...
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)
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 ...
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:Osso VR, Inc. based inSan Francisco, CALIFORNIA (USA)
The leading virtual reality surgical training and assessment platform. Osso VR gives medical device companies and healthcare professionals radically better ways to share, practice and learn new skills and procedures using virtual reality. From rare to routine, simple to the most ...
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 ...
Manufactured by:Elite Biomedical Solutions, LLC based inCincinnati, OHIO (USA)
Training for biomedical equipment technicians to meet the growing needs of the medical equipment ...
by:COBBLESTONE, a Division of The Center for Professional Advancement (CfPA) based inEast Brunswick, NEW JERSEY (USA)
For products that claim a desired Sterility Assurance Level (SAL), proof of a defined SAL (specification) is achieved through the product’s sterilization and sterility assurance controls. Compliance Observations cited each year by the FDA on Form 483s that relates to Sterilization and Sterility Assurance processes shows that there are deficiencies associated with these key processes that ...