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FAA Form - SUSPECTED UNAPPROVED PARTS NOTIFICATION

Date: March 18, 2010
Source: www.faa.gov

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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
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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
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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 ...

San Francisco, CA | Aug 6-7, 2020
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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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Quality Control Laboratory Compliance - cGMPs and GLPs: One and a Half Day Virtual Seminar

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FDA Recalls - Before You Start, and After You Finish : Virtual Seminar Seminar by Ex-FDA Official

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Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR: 2-Day...

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Ensuring Compliance with Advertising and Promotional Requirements for Drugs and...

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

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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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Measurement management systems - Requirements for measurement processes and measuring equipment
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Geometrical Product Specifications (GPS) - Geometrical tolerancing - Tolerances of form, orientation...
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Templates and Plans for Software Configuration Management Documents-Version 6.0
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Computer System Validation Master Plan
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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 Internal Audit Checklist, Procedure, and Forms
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Template for a Software Maintenance Plan - Fourth Edition
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Sarbanes Oxley Treasury Risks and Controls
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ISO 45001:2018 Flowcharts in MS Visio, SmartDraw, and PDF
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