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NSF International

NSF Health Sciences partners with life science companies, big and small, to provide highly customized end-to-end services throughout the product lifecycle. From early development to commercial manufacture and distribution, our expert services will assist you to:

Ensure regulatory compliance
Implement effective quality management systems
Maximize the contribution of your people
Assure the highest levels of product quality and safety
Improve your competitive edge in the marketplace

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Courses

E-learning
Auditing and Quality Management
ISO Length Price Location Reviews
Australia Medical Device Regulations – a Comprehensive Overview 2 hours 399 USD Online
Brazil Medical Device Regulations – a Comprehensive Overview 2 hours 399 USD Online
Canada Medical Device Regulations – a Comprehensive Overview 2 hours 399 USD Online
Cleaning Qualification 1.5 hours 117 USD Online
Computerized Systems Validation 0.7 hours 117 GBP Online
European Union Medical Device Regulation – EU MDR 2 hours 399 USD Online
Global Medical Device Regulatory Requirements (Five-Course Bundle) 1,400 USD Online
GMP for Engineers 0.7 hours 117 GBP Online
GxP Inspection Management Lifecycle 1 hour 117 GBP Online
Human Error Prevention: Best Practices from Industry 1 hour 117 GBP Online
Interface of GMP with GCP Quality Management Systems 1 Lesson 117 GBP Online
ISO 13485:2016 – International Medical Device Quality Management System (QMS) Standard 2 hours 400 USD Online
4.0 (2)
Japan Medical Device Regulations – a Comprehensive Overview 2 hours 399 USD Online
MDSAP and Regulatory Transitions – the Basics Virtual Training 2 hours 199 USD Online
5.0 (19)
Microbiology: The Basics 0.7 hours 117 GBP Online
Pharmaceutical EU Legislation Update 1 hour 117 GBP Online
Self-Inspections - How to Make Them Add Value to Your Organization 3 Lessons 117 GBP Online
SOP Writing and Revision 1.5 hours 117 GBP Online
The Roles and Responsibilities of an RP 0.7 hours 117 GBP Online
U.S. FDA Medical Device Complaint Handling and Servicing – Plus ISO 13485:2016 Requirements 1.5 hours 300 USD Online
United States Medical Device Regulations – a Comprehensive Overview 2 hours 399 USD Online
Quality Control
Design Controls for Medical Devices and IVDS 2.5 hours 199 USD Online
5.0 (2)
European Union in Vitro Diagnostic Device Regulation – EU IVDR 399 USD Online
U.S. FDA Presubmission (Q-Sub) Program – Requesting FDA Feedback 2 hours 299 USD Online
U.S. Quality Systems & Combination Products 399 USD Online
U.S.FDA Medical Device Reporting Requirements 1.5 hours 299 USD Online

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Contact

NSF International

789 N. Dixboro Road
48105 Ann Arbor Michigan

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www.nsf.org

Reviews

Scott
(5)
Content was perfect, instructors very knowledgeable and gave great examples.
Karla
(4)
Very well organized and delivery was excellent!
Anonymous
(5)
Great course to take!
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Training reviews
Institute rating
(4.9)
Based on 23 reviews