Refine by
Medical Flow Selector Device Training Courses Available In Iran
30 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: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: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 ...
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. ...
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: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: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: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:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
This package of 5 training courses is meant to give an exhaustive and in-depth understanding of the Japanese Pharmaceutical Affairs Law (PAL) including the 2005 revisions which are now in ...
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 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)
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 development paradigm. The complexity ...
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)
The main purpose of stability program is to evaluate a shelf life for a product to enter a market and before that determine a safe stability profile during clinical trial. There are many guidance which showcase the best practices how to achieve a successful stability program and then specific guidelines are formulated for a particular product ex – ICH regulatory guidance, QBD, PQS, ...
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)
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 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 ...