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FDA Guidance on Warning and Precautions Labeling for Drugs and Biological Products

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

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

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Case Management Boot Camp: Strategies for Success in the Acute Care Setting and Beyond!...

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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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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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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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