Audit - 3 Day Onsite All Inclusive - International 4 Part 11 - Electronic Records/Electronic

Part 11 - Electronic Records/Electronic Signatures (ERES) with Scope and Application

- ICH Q10 - Pharmaceutical Quality System

Packaging or Holding Produce

The Auditing Group's 21 CFR Part 820 QMSR Audit Check List with correlations to 21 CFR Part 820 & ISO 13485

Audit - 3 Day Onsite All Inclusive - International 4 Part 11 - Electronic Records/ElectronicTurnkey Audits & Training includes Airfare, Travel Rates, Hotel, Expenses & Reports (1 Draft & 1 Final). GMP Audits Drug, APIs, Excipients (DS DP) Medical Devices Part 820 QMSR ISO 13485 Supplier Audits, CMOs, CDMOs, CROs, Systems Laboratory Audits GLP GCLP, Part 58 OECD 21 CFR Part 11 Compliance & Validation Audits Cosmetics GMP Audits & Certificates Dietary Supplement GMP Audits & Certificates Clinical, CROs, GCLP, Investigator Sites Audits 503b