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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
Selection and Auditing of Analytical Contract Laboratories: Best Practices for Pharmaceutical Scientists

Selection and Auditing of Analytical Contract Laboratories: Best Practices for Pharmaceutical Scientists

  • Speaker: Daniel Norwood
  • Product ID: 705169
  • Duration: 90 Min
This webinar on selection and auditing of analytical contract laboratories will guide the participants to understand the process of CRO selection for analytical testing. Attendees will gain knowledge on the basic principles of quality auditing of a CRO; including audit planning, scheduling, conducting an audit, and the audit report process.
CD/Recorded
$249
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Recorded/CD
Military and USG Construction - the Differences Between OSHA and EM-385

Military and USG Construction - the Differences Between OSHA and EM-385

  • Speaker: John J Meola
  • Product ID: 705507
  • Duration: 60 Min
This webinar will discuss the major differences and distinctions between the USACE EM 385 and OSHA and how you can interpret and navigate both systems to assure a successful and accident free job.
CD/Recorded
$0
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Recorded/CD
Stability and Shelf Life of Medical Devices

Stability and Shelf Life of Medical Devices

  • Speaker: Stephanie Cooke
  • Product ID: 705485
  • Duration: 90 Min
This webinar will cover all relevant regulatory requirements (CFR, FDA, ISO, ASTM and European) for establishing the stability and determining the shelf-life of medical devices. Attendees will gain a better understanding of the design control process for designing medical devices.
CD/Recorded
$0
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Recorded/CD
Compliance Department Restructuring with the New Regulatory Demands

Compliance Department Restructuring with the New Regulatory Demands

  • Speaker: Carlo Chalhoub
  • Product ID: 705454
  • Duration: 60 Min
This webinar addresses recent changes in the compliance environment. It will also discuss the process for evaluating compliance department structure and the goals of compliance restructuring.
CD/Recorded
$0
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Recorded/CD
Is your Export Control Program Up to Standard? A How-to on Conducting a thorough Self-Assessment

Is your Export Control Program Up to Standard? A How-to on Conducting a thorough Self-Assessment

  • Speaker: Suzanne Bullitt
  • Product ID: 703205
  • Duration: 60 Min
This training on Export Administration Regulations (EAR) compliance will provide the attendees best practices for developing an export control program for conducting a thorough self assessment.
CD/Recorded
$149
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Recorded/CD
Develop a Device Master Record that can assist with Device History Record Review

Develop a Device Master Record that can assist with Device History Record Review

  • Speaker: Mary Nunnally
  • Product ID: 705328
  • Duration: 60 Min
This webinar provides a basic understanding of the records required to fulfill requirements of both US FDA 21CFR 820 and ISO 13485:2016 for establishment and maintenance of a Device Master Record. It will further discuss the responsibilities of various development team members such as R&D/engineering, operations, quality assurance, project management and executive management.
CD/Recorded
$0
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Recorded/CD
OSHA for Medical and Dental Offices

OSHA for Medical and Dental Offices

  • Speaker: Kelly D Ogle
  • Product ID: 705416
  • Duration: 60 Min
This webinar will discuss the most frequently found safety hazards in medical and dental offices, the OSHA requirements and standards that apply, and how to ensure compliance.
CD/Recorded
$0
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Recorded/CD
Equal Employment Opportunity (EEO) Beyond the Basics: Key Concepts and Principles

Equal Employment Opportunity (EEO) Beyond the Basics: Key Concepts and Principles

  • Speaker: Mary Gormandy White
  • Product ID: 705483
  • Duration: 60 Min
This webinar will focus on what supervisory and HR professionals at all levels need to know about EEO regulations and requirements, including protected characteristics, workplace harassment, retaliation and more.
CD/Recorded
$0
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Recorded/CD
The Past Isn't in the Past: Effecting Sound Employment Background Checks

The Past Isn't in the Past: Effecting Sound Employment Background Checks

  • Speaker: Jacquiline M Wagner
  • Product ID: 705489
  • Duration: 60 Min
This webinar will discuss the various laws covering background checks, common types, requirements for conducting background checks and more. It will also provide best practices to ensure compliance with the regulatory requirements.
CD/Recorded
$0
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Recorded/CD
Novel Foods Regulation in the European

Novel Foods Regulation in the European

  • Speaker: Vicente Rodriguez
  • Product ID: 705495
  • Duration: 60 Min
Learn what foods or food ingredients are considered 'Novel Foods'. Learn about novel foods applications, pre-marketing authorization procedures and the assessments required to demonstrate safety.
CD/Recorded
$0
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Recorded/CD
Good Manufacturing Practices for Active Pharmaceutical Ingredients (APIs)

Good Manufacturing Practices for Active Pharmaceutical Ingredients (APIs)

  • Speaker: Stephanie Cooke
  • Product ID: 705486
  • Duration: 90 Min
This webinar will cover ICH Q7, Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients (API). Attendees will gain a deeper understanding of the importance of GMPs for APIs, apply these principles in their current roles in order to better manage quality, make improvements, solve problems and make decisions.
CD/Recorded
$179
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Recorded/CD
ECCN & CCL - Classification, Exceptions, Documentation, License Requirements & More

ECCN & CCL - Classification, Exceptions, Documentation, License Requirements & More

  • Speaker: Suzanne Bullitt
  • Product ID: 704054
  • Duration: 60 Min
This webcast will provide an overview of U.S. Export Classification Control Numbers (ECCN) and making license determinations via the Commerce Control List (CCL).It will explain the “How to” classification breakdown and the considerations for commodity jurisdictions (CJs).
CD/Recorded
$179
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Recorded/CD
Wage and Hour Issues in the Age of Remote Work

Wage and Hour Issues in the Age of Remote Work

  • Speaker: Judith Bevis Langevin
  • Product ID: 705480
  • Duration: 60 Min
This webinar will focus on the federal wage and hour laws that apply to remote work. It will provide tips on how to manage remote work and best practices for responding to claims and audits related to remote work.
CD/Recorded
$179
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Recorded/CD
Exporting to Mexico Webinar Series 3: INCOTERMS Review and INCOTERM Common Practices in Mexico

Exporting to Mexico Webinar Series 3: INCOTERMS Review and INCOTERM Common Practices in Mexico

  • Speaker: Linda B Sarabia
  • Product ID: 704222
  • Duration: 60 Min
This third training program on exporting to Mexico will elucidate what are INCOTERMS, buyer and seller obligations, the global logistics process, INCOTERMS groups, documentation necessary to support the INCOTERM use and the Mexican customs criteria on INCOTERMS.
CD/Recorded
$229
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Recorded/CD
AES to ACE: Exporting from the U.S.A (ACE account, Documentation, Licensing, etc.)

AES to ACE: Exporting from the U.S.A (ACE account, Documentation, Licensing, etc.)

  • Speaker: Kimberly Daniels
  • Product ID: 705423
  • Duration: 90 Min
This webinar will discuss export product specifications, the changes from AES to ACE, how to apply for and manage an ACE account, fix issues with your ACE access, set-up your shipping documents in compliance with existing rules and regulations and more.
CD/Recorded
$179
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Recorded/CD
Exporting to Mexico Webinar Series 2: How to Settle Disputes with Mexican Customs

Exporting to Mexico Webinar Series 2: How to Settle Disputes with Mexican Customs

  • Speaker: Linda B Sarabia
  • Product ID: 704218
  • Duration: 60 Min
The second part of this exclusive Mexican customs training program will discuss Mexico import/export HTS codes, non-tariff barriers compliance, documentation compliance, customs administrative processes and more.
CD/Recorded
$229
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Recorded/CD
Implementing the new standard for product recall: AS/ISO 10393

Implementing the new standard for product recall: AS/ISO 10393

  • Speaker: Steve Hather
  • Product ID: 705478
  • Duration: 60 Min
This webinar will help you how to improve the effectiveness of recalls and enhance consumer safety, as well as protecting the company’s reputation.
CD/Recorded
$0
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Recorded/CD
NEW NACHA Rule: Third-Party Sender Registration - Are you Prepared?

NEW NACHA Rule: Third-Party Sender Registration - Are you Prepared?

  • Speaker: Donna K Olheiser
  • Product ID: 705469
  • Duration: 60 Min
Learn what a Third-Party Sender (TPS) is and how this impacts you. Take this training to understand how to determine if you have a Third-Party Sender relationship, the initial, basic registration information to submit to NACHA and the additional registration requirements if requested.
CD/Recorded
$199
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Recorded/CD
Using Records to Identify Root Causes of Non-Compliance

Using Records to Identify Root Causes of Non-Compliance

  • Speaker: John Fetzer
  • Product ID: 705345
  • Duration: 60 Min
This webinar will discuss the use of records to identify root causes of non-compliance in GLP or ISO 17025 compliant laboratory.
CD/Recorded
$0
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Recorded/CD
Duty Drawback in Canada - What you Need to Know

Duty Drawback in Canada - What you Need to Know

  • Speaker: Fabiola Ferrusquia
  • Product ID: 705468
  • Duration: 60 Min
Learn the options that the Duty Drawback in Canada can offer you to offset the expenses you have already incurred. We'll discuss conditions to be met, documentation requirements and more using practical examples.
CD/Recorded
$0
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