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Auditing - The Auditing Group and Validations.com GMP - GLP - GCP Part 11 Audits
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About Us / Contact Us. Software and Part 11. P Auditing - Remediation - Validation - Training. Boot Camp Training Seminar - All Inclusive! Training - Continental US - $5,995.00. Training - International - $7,995.00. 3 day intense Boot Camp Includes:. Travel, Hotel and Expenses*. Binders for 10 persons*. Certificates for 10 persons*. Additional Attendees $25.00 each,. Enhance your training experiance by having an optional Pre-Training GMP Audit conducted! 21 CFR Parts 210/211 Drug GMPs. GMPs - The Basics.
auditing.com
Auditing - The Auditing Group and Validations.com GMP - GLP - GCP Part 11 Audits
http://www.auditing.com/gcpaudits.htm
About Us / Contact Us. Software and Part 11. Good Clinical Practice Audits. The Auditing Group, Inc. (TAG). Has extensive experience assisting clients in the pharmaceutical, biotechnology, and medical device industries in all phases of Clinical Practices from Auditing to Training. US FDA - WHO - EMeA - GMP - GLP - GCP. From Feasibility, Phase I through IV, and then commercialization, The Auditing Group, Inc. has the expertise and background to support your projects. Audit Services for;. Laboratories &nda...
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Auditing - The Auditing Group and Validations.com GMP - GLP - GCP Part 11 Audits
http://www.auditing.com/part11audits1.htm
About Us / Contact Us. Software and Part 11. P Audits - Remediation - Validation - Training. 21 CFR Part 11 and Computer System Validation Audits. Assuring compliance with 21 CFR Part 11 regulations requires detailed examination and evaluation across systems, products, processes and functions within your organization. The Auditing Group has the perspective, objectivity, experience, expertise and services to help ensure your Company's compliance. Pre-Clinical and Clinical Research. The Auditing Group' aud...
auditing.com
Auditing - The Auditing Group and Validations.com GMP - GLP - GCP Part 11 Audits
http://www.auditing.com/glpaudits.htm
About Us / Contact Us. Software and Part 11. Good Laboratory Practice Audits. FDA - OECD - CLIA. The Auditing Group, Inc. has the laboratory expertise to assist with all of your inspection requirements. GLP Audits in support of:. Good Manufacturing Practices;. US FDA - WHO - EMeA - GMP - GLP - GCP. Drug - Medical Device - Biologics - Laboratory - Part 11 - Validation - Food - Nutraceutical. Not sure if your company can pass a GMP, GLP, GCP, Quality Systems, -. Part 11 and QSR Part 820 audit?
auditing.com
Auditing - The Auditing Group and Validations.com GMP - GLP - GCP Part 11 Audits
http://www.auditing.com/gmpaudits.htm
About Us / Contact Us. Software and Part 11. Good Manufacturing Practice (cGMP) Audits. FDA - WHO - EMeA. Drug, Medical Device, Laboratory, Clinical, Nutraceutical, and Biotech. Industries. The Auditing Group, Inc. (TAG). US FDA - WHO - EMeA - GMP - GLP - GCP. The interpretation and application of current Good Manufacturing Practice (cGMP) is critically important in order to meet the expectations and requirements of your customers as well as the US Food and Drug Administration (FDA). US Parts 210/211 and...
