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Consulting and training for FDA, CGMP, CE Marking, 510k, PMA, hazard analysis, FDA 483, consulting and training services for all industries including Medical Device, Pharmaceutical, Diagnostic, Bio-Tech, and Software worldwide. | fda-cgmp.com Reviews
https://fda-cgmp.com
Regulatory Experts provides services for consulting, training, and certification/compliance with FDA CGMP, Canadian, and European regulations.
fda-cgmp.com
Free Quotes and low price guaranteed for small business package onlinetraining, Guaranteed Certification, Consulting, Training 60-90 days for, ISO9000, ISO 9001, ISO 14001, ISO 14000, AS9100, OSHAS 18001, CE Mark, QS 9000,HACCP, ISO 13485, ISO 16949, T
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Toll Free # 1-888-476-9103. Please select the Service desired). Please select time period for service). Please select / specify location). Please select the desired specific service). Please select the desired specific standards). Software Verification and Validation. FDA QSR/GMP, ISO 13485 Audit. DA QSR/GMP, ISO 13485 Implementation Assistance. Medical Device License Submissions. FDA 483 and Warning Letter (response and resolution support). Agent for Non-USA Firms. Medical Device Reporting (MDR).
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AS 9100 - Certification, Training, and Consulting , online courses
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9110, 9120 Standards and Information. 100% Success Rate60-90 days*. Frequently Asked Questions about AS 9100. Key Steps for AS 9100 Certification. Online Training Link (Quality University). What is AS 9100? AS 9100 is international standard for the Quality Management System for the aerospace and defense industry. When was the standard released? The standard was released in October 1999. Who released the standard? What is the latest standard for AS 9100? The latest version is AS 9100 Rev C. AS9006 still a...
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ISO 13485 Standard and Certification. 100% Success Rate60-90 days*. Frequently Asked Questions about ISO 13485. Key Steps for ISO 13485 Certification. Online Training Link (Quality University). What is ISO 13485? ISO 13485 is international standard for the Quality Management System for the medical device industry. When was ISO 13485 released? ISO 13485 was released in 2003. What is the latest standard for ISO 13485? The latest version is ISO 13485 2003. Who needs to get ISO 13485 certified? Where can I g...
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ISO 22000 Steps for Certification. 100% Success Rate60-90 days*. Frequently Asked Questions about ISO 22000. Key Steps for ISO 22000 Certification. Online Training Link(Quality University). What is ISO 22000? ISO 22000 is a food safety standard that applies to any aspect of food-related business. When was ISO 22000 released? ISO 22000 was released in 2005. Who released ISO 22000? ISO 22000 was released by the International Standards Organization. What is the latest standard for ISO 22000? For assistance ...
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ISO 10002 Steps for Certification. 100% Success Rate60-90 days*. Frequently Asked Questions about ISO 10002. Key Steps for ISO 10002 Certification. What is ISO 10002? ISO 10002 is a customer satisfaction standard that assists companies in strategically understanding and managing their customers’ complaints. When was ISO 10002 released? ISO 10002 was released in 2004. Who released ISO 10002? ISO 10002 was released by the International Standards Organization. What is the latest standard for ISO 10002?
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HACCP Steps for Certification. 100% Success Rate60-90 days*. Frequently Asked Questions about HACCP. Key Steps for HACCP Certification. Online Training Link (Quality University). HACCP is a preventative safety approach that applies to all steps of the manufacture of food and pharmaceutical products. When was HACCP released? HACCP was initially released in 1972. HACCP was first released by Pillsbury as a food canning safety inspection. Who needs to get HACCP certified? What are the certification steps?
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TS 16949 Standard and. 100% Success Rate60-90 days*. Frequently Asked Questions about ISO/TS 16949. Online Training Link (Quality University). TS16949 is an international quality management standard that applies to the automotive industry. TS16949 was released by the automotive industry in an attempt to ensure the quality of products presented by automotive companies. Who needs to get TS16949 certified? What are the benefits of achieving TS16949 certification? What are the certification steps? ISO Accele...
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Consulting and training for FDA, CGMP, CE Marking, 510k, PMA, hazard analysis, FDA 483, consulting and training services for all industries including Medical Device, Pharmaceutical, Diagnostic, Bio-Tech, and Software worldwide.
FDA Regulatory Experts Group. FDA-REG provide consulting and training services for meeting requirements for all industries including Medical Device, Pharmaceutical, Diagnostic, Bio-Tech, Software, FDA, and CGMP for countries worldwide. A leader in consulting, training, development, verification, certification, auditing, translation services, for the following:. Software Verification and Validation. FDA QSR/GMP, ISO 13485 Audit. DA QSR/GMP, ISO 13485 Implementation Assistance. Agent for Non-USA Firms.
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Helping You Be Compliant and Profitable Until Year 2100 and Beyond. Highlights of completed FDA regulatory compliance projects - cGMP audits, remediation of FDA regulatory compliance critical gaps and simultaneous process and product quality improvement with no out-of-pocket expenses for medical device, pharmaceutical, biotechnology and life science companies. FDA Quality Systems Regulatory Compliance Audit of Class II Medical Device Product Line. Line clearance, foreign find, cGMP, FDA Approval or marke...
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Do you have a. Send us a Message! Compliance Consultants is a recognized leader in developing new medical devices and obtaining U.S. Food and Drug Administration "approval" for medical devices. We assist inventors world wide in developing new medical devices and shaping devices to fit through the FDA approval process. Why we are different. How we can charge less for more! Stamford, CT 06907 USA. Voice 203 329 2700 Fax 203 329 2345.
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