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Pharmaceutical - QMS & FDA Regulations

Pharmaceutical Training and Consulting Services

SAI Global delivers tailored and practical solutions to guide pharmaceutical companies in effectively applying and complying with the FDA cGMPs (21 CFR Parts 210, 211), ISO 9001 standards, Process Analytical Technologies (PAT) and the ICH guidance documents.

Our full-range consulting and training services will ensure that your company's quality system:

Is properly implemented
Provides controls
Produces consistency and quality
Manages and controls risks
Integrates and supports business processes and goals

Download your free copy of Quality Systems Approach to Pharmaceutical cGMPs.

Course Title	Course Schedule	At Your Location
Understanding and Implementing Quality Systems for the Pharmaceutical Industry	Schedule	Quote
Internal Auditor Training for FDA Regulated Industries (ISO 9001)	Schedule	Quote
RABQSA Certified Lead Auditor Training with Specific Reference to FDA Regulated Industries (ISO 9001)	Schedule	Quote
Process Mapping	Schedule	Quote
Understanding 21 CFR 210, 211		Quote
Executive Overview		Quote

Medical/Pharmaceutical Brochure

Download our medical/pharmaceutical business performance and regulatory compliance brochure.

Course Calendar

For a comprehensive listing of training dates and locations, view our online course calendar.

Want more information about our ISO 13485 - FDA Regulated Industries training program? Need ISO 13485 - FDA Regulated Industries on-site training or specialized support? Submit an ISO 13485 - FDA Regulated Industries inquiry, or call us at 1-800-374-3818.