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Home › Online Training ›  Documentation and Policy Management

Documentation and Policy Management Training - Live Webinars, Recordings & CDs

Learn the standards for documentation and management, maintain consistency with common law, regulatory requirements, ethical and current best practice requirements. On this page, browse a broad range of courses specially designed for you.
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Recorded/CD
Dietary Supplements Ingredient and Labeling Compliance

Dietary Supplements Ingredient and Labeling Compliance

  • Speaker: Marc Sanchez
  • Product ID: 702997
  • Duration: 60 Min
This webinar on dietary supplements will cover product ingredient reviews and FDA requirements for labeling your products in the US. You will learn how to avoid claims, what claims are permissible and how to remedy challenged claims.
CD/Recorded
$229
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Recorded/CD
Tax Levies and Creditor Garnishments Maintaining Compliance and Eliminating Problems

Tax Levies and Creditor Garnishments Maintaining Compliance and Eliminating Problems

  • Speaker: Vicki M. Lambert
  • Product ID: 702948
  • Duration: 90 Min
This HR regulations training will clearly explain how to handle tax levies and creditor garnishments efficiently and in compliance with the Federal and state requirements.
CD/Recorded
$149
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Recorded/CD
FDA and Social Media - How to Promote your Products Using Web 2.0 in Compliance with FDA and FTC Laws and Regulations

FDA and Social Media - How to Promote your Products Using Web 2.0 in Compliance with FDA and FTC Laws and Regulations

  • Speaker: Mark Gardner
  • Product ID: 702907
  • Duration: 90 Min
This webinar on FDA social media regulations will discuss the best practices utilized by medical device, drug and other FDA and FTC regulated industries when using social media channels, i.e., Web 2.0, like Facebook, Twitter, YouTube and LinkedIn to promote products.
CD/Recorded
$229
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Recorded/CD
Global Medical Device Laws and Regulations: US, EU, and Canada

Global Medical Device Laws and Regulations: US, EU, and Canada

  • Speaker: David Lim
  • Product ID: 702842
  • Duration: 90 Min
This training on global medical device regulations will discuss the regulatory framework for medical devices in US, EU and Canada. It will outline systematic methods to identify and meet regulatory requirements and streamline the regulatory process in these countries.
CD/Recorded
$50
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Recorded/CD
FDA's Revised 510(k) Process: The Medical Device Professional's Guide to Successfully Preparing 510(k) Submissions and Regulatory Compliance

FDA's Revised 510(k) Process: The Medical Device Professional's Guide to Successfully Preparing 510(k) Submissions and Regulatory Compliance

  • Speaker: Chris Cook
  • Product ID: 702963
  • Duration: 70 Min
This medical device 510(k) training will help you understand the basics of 510(k) submissions and discuss how to develop and execute an approval strategy ensuring the fastest possible path to market.
CD/Recorded
$229
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Recorded/CD
Understanding and Administrating COBRA: Avoiding Costly Conflicts with Government Agencies

Understanding and Administrating COBRA: Avoiding Costly Conflicts with Government Agencies

  • Speaker: Kenneth Sprang
  • Product ID: 702966
  • Duration: 60 Min
This COBRA (Consolidated Omnibus Budget Reconciliation Act) administration HR training course is designed to provide a comprehensive view of COBRA rule and it will also provide pragmatic tips on structuring and administering COBRA in your organization.
CD/Recorded
$50
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Recorded/CD
Must Have Enterprise Metrics for Financial Operations

Must Have Enterprise Metrics for Financial Operations

  • Speaker: Jon Casher
  • Product ID: 702961
  • Duration: 90 Min
This Must have Enterprise Metrics for Financial Operations webinar will cover the key performance indicators and metrics for your financial operations, issues encountered and effective usage of these key metrics for your business.
CD/Recorded
$50
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Recorded/CD
Interest Rate Risk Management - What the Regulators Want

Interest Rate Risk Management - What the Regulators Want

  • Speaker: Walt Tillman
  • Product ID: 702953
  • Duration: 90 Min
This webinar on Interest Rate Risk Management will highlight what the regulators expect community banks to do to effectively manage interest rate risk.
CD/Recorded
$149
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Recorded/CD
Medical Device Reporting for Manufacturers, Importers and Medical Device User Facilities

Medical Device Reporting for Manufacturers, Importers and Medical Device User Facilities

  • Speaker: Kosta Makrodimitris
  • Product ID: 702958
  • Duration: 90 Min
This webinar on Medical Device Reporting (MDR) will cover FDA requirements for importers, manufacturers and hospitals to report medical device adverse events. It will discuss current policies and guidances for Medical Device Reporting and provide update on upcoming regulations.
CD/Recorded
$149
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Recorded/CD
Advance HR Audit Techniques

Advance HR Audit Techniques

  • Speaker: Ronald Adler
  • Product ID: 702952
  • Duration: 60 Min
This webinar will provide advanced training in planning, executing, and reporting HR audits. Critical HR audit issues will be review including developing an HR audit plan, identifying audit stakeholders, critical employment practice areas, and analyzing key performance and risk indicators.
CD/Recorded
$149
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Recorded/CD
3-hr Virtual Seminar: Learning the OSHA Recordkeeping Analysis

3-hr Virtual Seminar: Learning the OSHA Recordkeeping Analysis

  • Speaker: William Principe
  • Product ID: 702168
  • Duration: 3 hrs
This 3-hr virtual seminar will show how OSHA analyzes record-keeping scenarios, applying the recordkeeping regulations, Frequently Asked Questions, and Interpretation Letters.
CD/Recorded
$299
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Recorded/CD
Common Import Compliance Problems

Common Import Compliance Problems

  • Speaker: Michael Laden
  • Product ID: 702878
  • Duration: 90 Min
This customs and trade compliance training will review a number of common issues and problems related to compliance with U.S. import laws and strategies or solutions for mitigating those issues.
CD/Recorded
$50
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Recorded/CD
Creating a Quality Assurance Program for (Clinical) Research Sites

Creating a Quality Assurance Program for (Clinical) Research Sites

  • Speaker: Amanda Shepler
  • Product ID: 702855
  • Duration: 60 Min
This clinical research QA training will provide practical advice for clinical research sites on when and how to get started with building their quality assurance program. A table of contents of the most critical SOPs will be provided.
CD/Recorded
$149
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Recorded/CD
MSRB Rule G-14: Reports of Sales or Purchases (RTTR) and FINRA Rule 6700: Trade Reporting and Compliance Engine (TRACE)

MSRB Rule G-14: Reports of Sales or Purchases (RTTR) and FINRA Rule 6700: Trade Reporting and Compliance Engine (TRACE)

  • Speaker: Kimberly McManus
  • Product ID: 702876
  • Duration: 60 Min
The MSRB and FINRA compliance training will teach you all of the complicated aspects of RTTR (Reports of Sales or Purchases) and TRACE (Trade Reporting and Compliance Engine) in a way that is laid out for ease of understanding and learning.
CD/Recorded
$149
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Recorded/CD
Asian Medical Device Laws and Regulations: China, Hong Kong, Japan and Korea

Asian Medical Device Laws and Regulations: China, Hong Kong, Japan and Korea

  • Speaker: David Lim
  • Product ID: 702841
  • Duration: 90 Min
This training on Asian medical device regulations will discuss the regulatory framework for medical devices in China, Hong Kong, Japan and Korea. It will outline systematic methods to identify and meet regulatory requirements and streamline the regulatory process in these Asian countries.
CD/Recorded
$229
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Recorded/CD
Country of Origin Marking for U.S. Imports

Country of Origin Marking for U.S. Imports

  • Speaker: Michael Laden
  • Product ID: 702849
  • Duration: 60 Min
This Country of Origin Marking for US Imports webinar will cover the requirements for marking imported goods and materials with the country of origin and conforming with U.S. Customs & Border Protection (CBP) rules.
CD/Recorded
$149
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Recorded/CD
What you Need to Know to Successfully Market and Sell an Over-the-Counter Drug Product in the United States; and Strategic Advice for Avoiding FDA Enforcement Action

What you Need to Know to Successfully Market and Sell an Over-the-Counter Drug Product in the United States; and Strategic Advice for Avoiding FDA Enforcement Action

  • Speaker: Karl M. Nobert
  • Product ID: 702840
  • Duration: 120 Min
This training on OTC drug marketing is intended to be a practice-based online workshop that will explain what you need to know to successfully market and sell an Over-the-Counter drug product in the United States; and provide strategic advice for avoiding FDA enforcement action.
CD/Recorded
$349
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Recorded/CD
Conventional Food Claims and Labeling

Conventional Food Claims and Labeling

  • Speaker: Bradley Johnson
  • Product ID: 702695
  • Duration: 90 Min
This webinar will cover how conventional food companies should label their products for the US market per FDA requirements, considerations avoid claims, building regulatory compliance into company programs for development and launch of properly labeled dietary supplements.
CD/Recorded
$229
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Recorded/CD
Dietary Supplements Labeling - Avoiding Claims that Invite Scrutiny and Penalties

Dietary Supplements Labeling - Avoiding Claims that Invite Scrutiny and Penalties

  • Speaker: Marc Sanchez
  • Product ID: 702807
  • Duration: 60 Min
This training will cover FDA requirements for labeling dietary supplements. It will show how you can avoid dietary supplement labeling claims by properly labeling your products for the US market per FDA requirements.
CD/Recorded
$229
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Recorded/CD
Dietary Supplement Adverse Event Reporting and Recordkeeping Requirements under the Dietary Supplement and Nonprescription Drug Consumer Protection Act

Dietary Supplement Adverse Event Reporting and Recordkeeping Requirements under the Dietary Supplement and Nonprescription Drug Consumer Protection Act

  • Speaker: Katherine Giannamore
  • Product ID: 702756
  • Duration: 60 Min
This webinar on dietary supplement adverse event reporting will explain the requirements under federal law as to when serious adverse event reports must be submitted to the FDA, what information and when it must be submitted. In addition, it will highlight the recordkeeping requirements under the law pertaining to all adverse event reports.
CD/Recorded
$229
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