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Medical Device Manufacturer Training Courses
11 training items found
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 ...
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 ...
by:ComplianceOnline based inSan Jose, CALIFORNIA (USA)
This comprehensive training package of 7 courses is aimed at helping companies to be compliant and streamline the robust supply chain planning, processes, risk management etc by maintaining regulatory guidelines. Implementing Robust Supply chains for life-sciences companies are important now and growing in importance as device manufacturers outsource products and ...
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: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)
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, ...
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)
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 ...
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)
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)
The following is a pack of 4 best-selling training CDs for sales, marketing & regulatory professionals in the Medical Device 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 ...