50 Handbooks at $9
- Parts 210/211 Drug GMPs
OECD - General Principles of GLP Series 1
Canadian and European Medical Device Regulations
Electronic Signatures with Scope and Application
Audit and Training - 2 Day Onsite All-Inclusive Audit with 1 Day Training - U.S. 58 50 Handbooks at $9Turnkey 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