NOBLITT & RUELAND
Noblitt & Rueland specialize in technical FDA including quality systems, submissions, design control, risk management, and software.
NOBLITT & RUELAND
Industry:
Consulting Risk Management Software
Address:
Irvine, California, United States
Country:
United States
Website Url:
http://www.noblitt-rueland.com
Status:
Active
Contact:
+1-949-398-5222
Email Addresses:
[email protected]
Official Site Inspections
http://www.noblitt-rueland.com
- Host name: 108-179-232-88.unifiedlayer.com
- IP address: 108.179.232.88
- Location: Houston United States
- Latitude: 29.8284
- Longitude: -95.4696
- Metro Code: 618
- Timezone: America/Chicago
- Postal: 77092
More informations about "Noblitt & Rueland"
Medical Device Regulatory Consulting & Training | Noblitt
Noblitt & Rueland has over 25 years of experience helping Medical Device manufacturers with FDA & International Regulatory and Compliance issues. From Consulting services by experts …See details»
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Noblitt & Rueland is the leading medical device consulting firm specializing in technical FDA & international regulatory issues including Quality Systems, Submissions, Design Control, Risk …See details»
Medical Device FDA & International Training | Noblitt & Rueland
Entire product teams and companies can be trained at one time assuring the understanding and efficient implementation of new processes, philosophies, requirements, and regulatory …See details»
Noblitt & Rueland - Crunchbase Company Profile & Funding
Noblitt & Rueland specialize in technical FDA including quality systems, submissions, design control, risk management, and software.See details»
Medical Device FDA & International Consulting - Noblitt & Rueland
Get expert medical device regulatory & quality consulting. Check out our consulting services & training courses and take advantage of our 25+ years experience.See details»
Medical Device Regulatory Training Course List - Noblitt & Rueland
Learn about FDA investigations & enforcement from a 30 year veteran of FDA and Investigations. Impact of Usability, IEC 62304, & SaMD. Learn what FDA expects for a compliant Complaint …See details»
Noblitt And Rueland Company Profile - Dun & Bradstreet
Find company research, competitor information, contact details & financial data for Noblitt And Rueland of Tustin, CA. Get the latest business insights from Dun & Bradstreet.See details»
FDA Quality System Regulation & Inspections - Device Training
This course will provide an understanding of FDA’s Quality System Regulation (QSR), 21 CFR 820, for medical device manufacturers and how it impacts all departments and personnel …See details»
Noblitt & Rueland - Overview, News & Similar companies
View Noblitt & Rueland (www.noblitt-rueland.com) location in California, United States , revenue, industry and description. Find related and similar companies as well as employees by title and …See details»
Auditing Services for Medical Device Quality Systems - noblitt …
At Noblitt & Rueland, we offer comprehensive medical device quality system (QMS) audits to help you achieve and maintain compliance with FDA 21 CFR Part 820, ISO 13485 and MDSAP …See details»
Description of Training & Consulting Services | Noblitt & Rueland
Understand how Noblitt & Rueland can help you with our consulting and training services.See details»
Noblitt & Rueland: Contact Information
Give us a call or send us an e-mail. We will be happy to discuss your needs and how we can assist you.See details»
Design Control Compliance for FDA & ISO - Noblitt & Rueland
Overview: FDA investigators are inspecting and pursuing enforcement activities for non-compliant Design Control violations. FDA has published that 68% of firms inspected had potential design …See details»
Auditing Techniques for Medical Device Quality Systems-Training
Auditing Quality Systems for FDA & ISO Compliance - Training Course. Virtual & On-site available. Train your team to perform vendor & internal audits.See details»
IEC 60601-1 3rd Edition & Certification Requirements - Noblitt
Understanding of IEC 60601-1 and what has changed with the amendments. How to meet usability (IEC 60601-1-6) and alarm (IEC 60601-1-8) requirements. Review of EMC …See details»
Software Verification & Validation - Medical Device Training
FDA has released a revised guidance document on software which impacts medical device manufacturers. This course will help you understand software verification and validation and …See details»
Risk Management, ISO 14971 & FDA - Medical Device Training
Understand ISO 14971 and how to implement to comply with FDA & ISO / EN / MDR / IVDR requirements. How to implement Risk Management as part of Design Control. Differences …See details»
Noblitt & Rueland: Consulting Opportunities
Are you an independent, experienced medical device consultant or service provider? Send us your information to explore project opportunities.See details»
ISO 13485 International Medical Device Quality System Training
Overview: This course will discuss the ISO 13485:2016, explain the differences between and what needs to be modified in a FDA (21 CFR Part 820) compliant Quality System in order to be …See details»
FDA Electronic Recordkeeping & Signatures - 21 CFR Part 11
FDA has published the “Scope and Application” guidance as related to 21 CFR Part 11 in addition to the withdrawal of multiple Part 11 guidance and compliance policy. It is important for …See details»