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Regulation P - PRIVACY OF CONSUMER FINANCIAL INFORMATION

By: www.federalreserve.gov
Date: November 11, 2011

Abstract:

The US Federal Reserve Board’s Regulation P or Privacy of Consumer Financial Information (12 CFR 216) regulates the use of nonpublic personal information about consumers by financial institutions.

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Compliance Trainings

Pregnancy in the Workplace: Strategies to Protect Your Organization from Pregnancy Discrimination Claims
By - Christopher W. Olmsted
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How to Vet an IRB: Expose and Fix Problems Before They Threaten Your Trial
By - Madhavi Diwanji
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DMR & DHR - What Is Really Required
By - Daniel O Leary
On Demand Access Anytime

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Compliance Standards

Checklist for applying IEC 62304:2015 ''Medical Device Software - Software Life Cycle Processes''
Price: $330Add to Cart

A Software Engineering Kit – Composed of Templates for Key Software Engineering Process Plans
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ISO/IEC 20000-1:2011 “Information Technology – Service Management –Part 1: Service Management System Requirements”
Price: $330Add to Cart

Software Quality Kit
Price: $748Add to Cart

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FDA Regulations for Marketing OTC Drugs in the U.S.
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Effective Annual U.S. FDA CGMP Training
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CDISC Mapping 1: Specifications and FDA Requirements
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Extractables and Leachables in Early Phase Development
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Advanced Tax Return Analysis for the Banker
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1099 & W-9 Update - Complying with IRS Information Reporting Guidelines
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OSHA Recordkeeping for 2015: Beyond the OSHA 300 Summary
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Form I-9 and E-Verify, getting and staying compliant
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REACH and RoHS Compliance: Protecting Revenues with Advanced Compliance: 2-Day In-Person ...

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Preparing for FDA's New Import/Export Trauma in 2020: 2-Day In-Person Seminar by Ex-FDA Official

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Managing Domestic and Foreign FDA Inspections and the COVID-19 Impact: 2-Day In-Person Seminar...

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Quality Control Laboratory Compliance - cGMPs and GLPs: One and a Half Day Virtual Seminar

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Data Integrity: FDA/EU Requirements and Implementation: 2-Day Workshop

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21 CFR Part 11 Compliance for SaaS/Cloud Applications: 2-Day Virtual Seminar

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Supplier and Contract Manufacturer Management: 2-Day Virtual Seminar

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Project Management for Human Resources: 3-Day Certification Program

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General requirements for the competence of testing and calibration laboratories
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IEC 62304:2015 ''Medical Device Software - Software Life Cycle Processes''
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IEC 62304:2015 ''Medical Device Software - Software Life Cycle Processes''
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ISO 45001:2018 Gap Analysis Checklist
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Zero Acceptance Number Sampling Plan for Receiving, In-Process and Final Inspection
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Standard Operating Procedure: FDA Inspections
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AS9003 Comprehensive Quality System Kit for Inspection and Test Quality Control System
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ISO 45001:2018 Flowcharts in MS Visio, SmartDraw, and PDF
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Regulation P - PRIVACY OF CONSUMER FINANCIAL INFORMATION

Compliance Trainings

Compliance Standards