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Regulatory Document Training Courses

4 training items found

NSR Online Training

NSR Online Training

by:RTP Environmental Associates, Inc.   based inGreen Brook, NEW JERSEY (USA)
NSRonline Plus is the premier online reference for information on the federal Clean Air Act New Source Review (NSR) program. NSRonline Plus is a subscription-based web service offering electronic access to the Advanced New Source Review Workshop course outline, which provides up-to-date information on the entire range of EPA policy documents (approximately 1,500 documents and 20,000 pages of ...
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Public Environmental Training

Public Environmental Training

by:OSE Training Group, LLC   based inGlenelg, MARYLAND (USA)
Our open enrollment public environmental training seminars are conducted in a small personal seminar format. You and your classmates will learn through presentations and open discussions. ...
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Premarket Notification to Recalls - Comprehensive Medical Device Regulations Training Package

Premarket Notification to Recalls - Comprehensive Medical Device Regulations Training Package

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 ...
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EU Medical Device Regulations - Comprehensive Compliance Training Course

EU Medical Device Regulations - Comprehensive Compliance Training Course

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 Directive and ISO Certification ...
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