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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
Employee Fraud Detection and Prevention

Employee Fraud Detection and Prevention

  • Speaker: Peter Goldmann
  • Product ID: 702440
  • Duration: 90 Min
This 90-minute webinar will summarize current and emerging cyber-threats and provide latest insights and advice from experts on how to protect your organization from individuals - both inside and outside of your organization.
CD/Recorded
$99
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Recorded/CD
Meaningful Safety Metrics - What Every Safety Professional Should Know

Meaningful Safety Metrics - What Every Safety Professional Should Know

  • Speaker: Michael Lawrence
  • Product ID: 702432
  • Duration: 60 Min
This webinar will guide you in establishing the right safety metrics for your organization. You will learn about steps you can implement to improve your organization's safety performance.
CD/Recorded
$149
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Recorded/CD
Validation and use of Excel spreadsheets in FDA regulated environments

Validation and use of Excel spreadsheets in FDA regulated environments

  • Speaker: Alfonso Fuller
  • Product ID: 701327
  • Duration: 60 Min
This FDA validation training will describe methods for planning and executing spreadsheet validations that satisfy FDA requirements.
CD/Recorded
$299
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Recorded/CD
Procure to Pay (P2P) Metrics and Dashboards

Procure to Pay (P2P) Metrics and Dashboards

  • Speaker: Chris Doxey
  • Product ID: 702370
  • Duration: 60 Min
This session will provide a roadmap for the implementation of key metrics that can be used in formulating a P2P Dashboard. Attendees will learn how to actually use metrics and trends to develop areas for business process improvement.
CD/Recorded
$149
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Recorded/CD
Developing and Implementing Golden Parachute Agreements

Developing and Implementing Golden Parachute Agreements

  • Speaker: Michael Melbinger
  • Product ID: 702363
  • Duration: 90 Min
This 90-minute webinar will provide practical tips on how you can develop and implement Golden Parachute Agreements that fulfill tax code and federal securities law requirements, pass investor and media scrutiny, and avoid potentially high stakes litigation.
CD/Recorded
$149
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Recorded/CD
Best Practices for Maintaining an IND and IDE Application with FDA

Best Practices for Maintaining an IND and IDE Application with FDA

  • Speaker: Mukesh Kumar
  • Product ID: 702254
  • Duration: 60 Min
This webinar on IND and IDE Application management will help you understand the current FDA requirements for IND and IDE application post initial approval to proceed with the clinical trial.
CD/Recorded
$229
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Recorded/CD
Good Documentation Practices for GXPs

Good Documentation Practices for GXPs

  • Speaker: Anne E Maczulak
  • Product ID: 701320
  • Duration: 60 Min
This webinar on Good Documentation Practices will review the FDA requirements for documenting data in preclinical and clinical studies and manufacturing activities.
CD/Recorded
$229
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Recorded/CD
Archiving GLP Records: How Archiving Makes or Breaks the Audit

Archiving GLP Records: How Archiving Makes or Breaks the Audit

  • Speaker: Anne E Maczulak
  • Product ID: 701505
  • Duration: 60 Min
This webinar on archiving GLP records will discuss the options for managing large archiving facilities to small facilities with one-room archives. You will receive practical tips on how to correct mistakes that agencies have cited regarding archiving.
CD/Recorded
$349
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Recorded/CD
3-hr Virtual Seminar- Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada

3-hr Virtual Seminar- Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada

  • Speaker: David Lim
  • Product ID: 702240
  • Duration: 3 hrs
This 3-hr virtual seminar will discuss the requirements and compliance in medical device adverse event reporting and medical device surveillance/vigilance system in the US, Europe and Canada. It is designed to help the audience with their global compliance in adverse event reporting and surveillance/vigilance system during pre- and post-marketing.
CD/Recorded
$249
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Recorded/CD
Webinar: When Do You Need a 510K?

Webinar: When Do You Need a 510K?

  • Speaker: Charles R. McConachie
  • Product ID: 702249
  • Duration: 90 Min
This 90-minute webinar will help you understand the 510K process including some history about 510ks versus PMAs and give you the necessary information to know when to file a 510k, as opposed to a PMA, or to not file any 510K of a new or existing medical device.
CD/Recorded
$50
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Recorded/CD
OSHA Recordkeeping: Recent Recordkeeping Interpretations

OSHA Recordkeeping: Recent Recordkeeping Interpretations

  • Speaker: William Principe
  • Product ID: 702225
  • Duration: 90 Min
This 90-minute OSHA Recordkeeping training class will incorporate the lessons learned from OSHA’s recent Interpretation Letters into the existing OSHA recordkeeping analysis as well as OSHA’s current Frequently Asked Questions. In this interactive program, OSHA recordkeeping scenarios will be used so that the rules articulated in the recent Interpretation Letters can be applied to real-life factual situations that arise in your work environments.
CD/Recorded
$119
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Recorded/CD
How to Write SOPs: Tips on Writing the Perfect Document to Impress the FDA

How to Write SOPs: Tips on Writing the Perfect Document to Impress the FDA

  • Speaker: Mukesh Kumar
  • Product ID: 701913
  • Duration: 60 Min
This webinar on SOPs will instruct you in creating, managing and implementing adequate SOPs that can impress even the FDA inspectors.
CD/Recorded
$299
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Recorded/CD
Introduction to FDA Good Documentation Practices

Introduction to FDA Good Documentation Practices

  • Speaker: Chris Whalley
  • Product ID: 700127
  • Duration: 60 Min
This FDA Good Documentation Practices training will introduce and explain the concept of Good Documentation Practices, and provide real-world examples of how to, and how not to, use GDPs.
CD/Recorded
$299
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Recorded/CD
Collection of Applicant Flow Data, Data on Hiring Process Flow, and Use of it in an Affirmative Action Plan

Collection of Applicant Flow Data, Data on Hiring Process Flow, and Use of it in an Affirmative Action Plan

  • Speaker: Joe Gross
  • Product ID: 702165
  • Duration: 90 Min
This 90-minute webinar on creating an Affirmative Action Plan will show how you can collect Applicant Flow data, track information from the hiring process and use it to build Affirmative Action Plans.
CD/Recorded
$199
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Recorded/CD
Documentation and Discipline: Solutions to Successful Outcomes

Documentation and Discipline: Solutions to Successful Outcomes

  • Speaker: Marna Hayden
  • Product ID: 702147
  • Duration: 60 Min
This webinar on Documentation and Discipline will cover discipline policies, standards of conduct, and the process of counseling and progressive discipline, up to and including terminations. It will also cover legal aspects of discipline and discharge.
CD/Recorded
$399
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Recorded/CD
How to Document Employment Decisions Properly So It Will Stand Up in Court

How to Document Employment Decisions Properly So It Will Stand Up in Court

  • Speaker: Susan Fahey Desmond
  • Product ID: 702161
  • Duration: 90 Min
This 90 minute webinar on legal HR documentation will address why documentation is important in every employment decision you make. Learn from real life lessons, from actual court cases, of how documentation helped an employer to win its case and how wrong documentation ensured a loss.
CD/Recorded
$399
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Recorded/CD
Full day Virtual Seminar: Drug Master Files - Understanding and Meeting your Global Regulatory and Processing Responsibilities

Full day Virtual Seminar: Drug Master Files - Understanding and Meeting your Global Regulatory and Processing Responsibilities

  • Speaker: Robert J Russell
  • Product ID: 702039
  • Duration: 6 hrs
This DMFs (Drug Master Files) training will discuss the current review and enforcement climate within FDA and the manner in which drug master files (DMFs) are reviewed by FDA personnel. Besides the US, the use of DMFs in the EU, Japan, Canada and Australia will also be discussed. Similarities and differences to the U.S. system will be highlighted.
CD/Recorded
$1099
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Recorded/CD
Little-Known Risks of Personnel Files

Little-Known Risks of Personnel Files

  • Speaker: Joe Gross
  • Product ID: 701965
  • Duration: 60 Min
This webinar will explain the different types of Personnel Files. Attendees will learn about the types of personnel files that need to be separated from other types, and those that require separate security measures.
CD/Recorded
$449
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Recorded/CD
The FDA's final Medical Device Data System (MDDS) rule and its implications for currently regulated and unregulated vendors and providers

The FDA's final Medical Device Data System (MDDS) rule and its implications for currently regulated and unregulated vendors and providers

  • Speaker: Tim Gee
  • Product ID: 700959
  • Duration: 65 Min
The presentation will consider potential impacts of the rule on regulated and unregulated vendors, and providers. This session will survey the market affected by the proposed rule, and define the common components and capabilities of these systems.
CD/Recorded
$299
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Recorded/CD
Fundamentals of OSHA Injury and Illness Recordkeeping with Key Interpretations

Fundamentals of OSHA Injury and Illness Recordkeeping with Key Interpretations

  • Speaker: Bill Taylor
  • Product ID: 701910
  • Duration: 80 Min
This OSHA injury and illness recordkeeping webinar will explain how to determine work relatedness and determine which cases are recordable on the OSHA form 300. It will also explain key and recent OSHA recordkeeping interpretations.
CD/Recorded
$545
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