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Pharma Compliance Partners, LLC.

Pharma Compliance Partners, LLC. Collaborating with pharmaceutical companies and clinical service providers in the areas of quality assurance compliance, project management, clinical research and device monitoring, regulatory affairs (submissions, review, and strategy) and operations. 21 CFR Part 820. 21 CFR Part 11. Vendor audits (GMP, GLP, GCP). Clinical Study Report Audits/Reviews. Part 11 System Audits. Quality and Clinical Research Training. Clinical Monitoring - Drug and Device.

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Pharma Compliance Partners, LLC. | phrmacompliance.com Reviews
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Pharma Compliance Partners, LLC. Collaborating with pharmaceutical companies and clinical service providers in the areas of quality assurance compliance, project management, clinical research and device monitoring, regulatory affairs (submissions, review, and strategy) and operations. 21 CFR Part 820. 21 CFR Part 11. Vendor audits (GMP, GLP, GCP). Clinical Study Report Audits/Reviews. Part 11 System Audits. Quality and Clinical Research Training. Clinical Monitoring - Drug and Device.
<META>
KEYWORDS
1 fda gcp
2 ich gcp
3 eu directive
4 quality services include
5 investigational site audits
6 bioanalytical laboratory audits
7 general system/internal audits
8 pre inspection preparation
9 process implementation
10 project management
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fda gcp,ich gcp,eu directive,quality services include,investigational site audits,bioanalytical laboratory audits,general system/internal audits,pre inspection preparation,process implementation,project management,technical writing,medical writing,email
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Pharma Compliance Partners, LLC. | phrmacompliance.com Reviews

https://phrmacompliance.com

Pharma Compliance Partners, LLC. Collaborating with pharmaceutical companies and clinical service providers in the areas of quality assurance compliance, project management, clinical research and device monitoring, regulatory affairs (submissions, review, and strategy) and operations. 21 CFR Part 820. 21 CFR Part 11. Vendor audits (GMP, GLP, GCP). Clinical Study Report Audits/Reviews. Part 11 System Audits. Quality and Clinical Research Training. Clinical Monitoring - Drug and Device.

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judilhendricksdesign.com judilhendricksdesign.com

Judi L Hendricks Design - About JLH Design

http://www.judilhendricksdesign.com/about.html

Has been specializing in case report form design for the pharmaceutical research industry for over twenty years, both as a full-time member of Data Management research teams (1987-1997) and as a freelance design consultant (1997–present). Judi has worked with dozens of research firms studying medical indications ranging from asthma to infertility to oncology, giving her a wealth of experience from which to draw. With Katie Baum, and published several articles on the ArtClay. Also has a background in psyc...

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Pharma Compliance Partners, LLC.

Pharma Compliance Partners, LLC. Collaborating with pharmaceutical companies and clinical service providers in the areas of quality assurance compliance, project management, clinical research and device monitoring, regulatory affairs (submissions, review, and strategy) and operations. 21 CFR Part 820. 21 CFR Part 11. Vendor audits (GMP, GLP, GCP). Clinical Study Report Audits/Reviews. Part 11 System Audits. Quality and Clinical Research Training. Clinical Monitoring - Drug and Device.

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