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GMP Aud |
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Training Services - In house / Webinars |
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consultants and traininers are
has extensive experience within the FDA regulated
industries working under the various standards (cGMP,
cGCP, cGLP, Systems) with one goal, to provide
reliable auditing, validation, consulting, training,
and quality assurance services that efficiently
provide the assistance needed to help our clients
succeed.
At TAG,
stand behind all of our audits, training services,
site remediation and validation projects, even in
times of ‘for-cause’.
It is
our objective to become your partner in your quality
initiative! |
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Not
sure if your company can pass a
GMP, GLP, GCP, Quality Systems, -
Part 11 & QSR Part 820 audit?
Get an independent assessment of your quality and regulatory
readiness today!
Or call 856-596-2333
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GMP, GCP, GLP, QS and Part 11 / Systems Audit
21 CFR Part(s) 11, 210/211, 820, ICH Q7
Food and Supplement GMP Audits
Mock FDA - EMEA Audits
Pre-Site Inspections - 'For-Cause'
Quality Assurance Audits
Quality System Audits - Part 820
SOPs, Quality Assurance and Standards Audits
GMP - Good Manufacturing Practice Audit
GCP - Clinical Audits - Regulatory Audits
Equipment Validation Documentation Audit
Software / Systems Validation Audits
Part 11 / Annex 11 Compliance
Vendor & Supplier Audits -
CMOs, Laboratories, API Manufacturers
CROs, Investigators, Monitors, and Study Sites
Database Audits, SAS, CMMS, eDC, eCFR, Safety
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Project Management Services
Gantt and Timeline Development
Template Implementation
SOP Development
Development
Part 11 Initiatives
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