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Home › Online Training ›  Regulatory Affairs

Regulatory Affairs Training - Live Webinars, Recordings & CDs

Hundreds of regulatory affairs specialists each year use ComplianceOnline courses to learn skills and get a clear understanding of specific regulatory requirements needed to succeed in their role. On this page, you will find a broad range of courses specially designed for you. Whether you work in the pharmaceutical, medical device, and equipment, biotechnology, cosmetics, research, or regulatory agencies, or within legal, marketing, and scientific consulting firms, you can get acquainted with the regulatory requirements and guidance for your industry. With the knowledge you gain, you will learn how to apply the regulations in a compliant manner into the actual materials that your company manufactures. You will be in a better position to understand the risks your organization faces. You will get a robust understanding of compliance within the scope of your duties. With the knowledge you gain, you can evaluate current practices and make improvements where necessary. Join them!
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Recorded/CD
3-hr Virtual Seminar: New Changes to the HIPAA Regulations - What's about to go into effect and what else is on the way

3-hr Virtual Seminar: New Changes to the HIPAA Regulations - What's about to go into effect and what else is on the way

  • Speaker: Jim Sheldon-Dean
  • Product ID: 702181
  • Duration: 3 hrs
This 3-hr virtual seminar on the New Changes to the HIPAA Regulations will discuss the details of changes, how these changes will affect your organization and your Business Associates, new penalties and enforcement of HIPAA.
CD/Recorded
$599
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Recorded/CD
3-hr Virtual Seminar: SOX - Internal Controls for Accounts Receivable

3-hr Virtual Seminar: SOX - Internal Controls for Accounts Receivable

  • Speaker: Mike Morley
  • Product ID: 702163
  • Duration: 3 hrs
This 3-hr presentation covers specific issues affecting Credit and Accounts Receivable, including Credit Risk Management, the adequacy of provisions for Bad Debt, Collection Procedures, dependence on processes outside the credit department, and outside the company. This seminar will help Credit Professionals understand their responsibilities and duties so that they can be confident that their Credit and Accounts Receivable processes are Sarbanes-Oxley compliant.
CD/Recorded
$599
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Recorded/CD
Critical Issues to Consider in Planning for and Providing Telemedicine Programs

Critical Issues to Consider in Planning for and Providing Telemedicine Programs

  • Speaker: Yadin David
  • Product ID: 702093
  • Duration: 60 Min
This webinar on Telemedicine Programs will focus on critical issues to be addressed before joint program connecting remote and central locations is planned and implemented. New technical and regulatory developments like that of FDA on Medical Data Device Systems (MDDS) and its implications on the telehealth community will be discussed.
CD/Recorded
$499
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Recorded/CD
US FDA requirements for food contact packaging material compliance

US FDA requirements for food contact packaging material compliance

  • Speaker: Thomas J. Dunn
  • Product ID: 701958
  • Duration: 60 Min
This webinar will identify components of a valid letter of guarantee for the food processor and the determinations that food packaging supplier must make in issuing the guarantee, certifying that they comply with US FDA regulations.
CD/Recorded
$549
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Recorded/CD
Regulation of printing inks on food contact packaging materials in the US & EU

Regulation of printing inks on food contact packaging materials in the US & EU

  • Speaker: Thomas J. Dunn
  • Product ID: 701960
  • Duration: 60 Min
This webinar addresses new test methods for quantifying migration of Printing inks on food packaging materials into the packaged food and how they affect food safety law compliance.
CD/Recorded
$549
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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
ITAR Compliance: A Guide to the International Traffic in Arms Regulations

ITAR Compliance: A Guide to the International Traffic in Arms Regulations

  • Speaker: Michelle Schulz
  • Product ID: 701900
  • Duration: 60 Min
This webinar will help you Gain a better understanding of your responsibilities as an exporter under the ITAR. Learn about the laws governing defense articles and services, how to comply with the regulations, and develop an effective ITAR compliance program.
CD/Recorded
$299
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Recorded/CD
Food Recalls - Planning and conducting a Food Recall and Crisis Communication

Food Recalls - Planning and conducting a Food Recall and Crisis Communication

  • Speaker: Irwin Pronk
  • Product ID: 701108
  • Duration: 90 Min
This Food Recall training will help you create a robust process for planning and conducting a food recall and crisis communication. It will help each department anticipate their roles and responsibilities so your company’s response will be effective and swift.
CD/Recorded
$299
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Recorded/CD
360 Degree Approach to Health Information Privacy

360 Degree Approach to Health Information Privacy

  • Speaker: James Bone
  • Product ID: 702049
  • Duration: 65 Min
This Health Information Privacy Compliance training will provide an outline and roadmap for developing a risk-based approach to compliance.
CD/Recorded
$499
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Recorded/CD
New amendments of Critical parameters in Canadian Clinical trials

New amendments of Critical parameters in Canadian Clinical trials

  • Speaker: Calin Popa
  • Product ID: 701871
  • Duration: 60 Min
Learn about last changes in Canadian ethics regulations, understand how to apply the change in the day-to-day work.
CD/Recorded
$345
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Recorded/CD
Understanding the Final Regulations under the Americans with Disabilities Amendments Act

Understanding the Final Regulations under the Americans with Disabilities Amendments Act

  • Speaker: Susan Fahey Desmond
  • Product ID: 702011
  • Duration: 57 Min
This ADA Amendments webinar will help you clearly understand the EEOC's final regulations on The Americans with Disabilities Act and what it means to your company.
CD/Recorded
$499
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Recorded/CD
Good manufacturing practices for food contact packaging producers in the US and EU

Good manufacturing practices for food contact packaging producers in the US and EU

  • Speaker: Thomas J. Dunn
  • Product ID: 701959
  • Duration: 57 Min
This food safety webinar addresses components of Good Manufacturing Practices that packaging material suppliers should follow for adherence to both regulatory and voluntary standards protocols
CD/Recorded
$549
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Recorded/CD
The Pros and Cons of Alternative Working Arrangements and Regulatory Requirements in Implementing Such Programs

The Pros and Cons of Alternative Working Arrangements and Regulatory Requirements in Implementing Such Programs

  • Speaker: Susan Fahey Desmond
  • Product ID: 701939
  • Duration: 60 Min
Learn the regulatory requirements and legal ramifications of alternative working arrangements - flextime programs, job sharing, telecommuting, etc.
CD/Recorded
$549
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Recorded/CD
PPACA - Large Employer Penalties Overview

PPACA - Large Employer Penalties Overview

  • Speaker: Tony Gutierrez,Teresa C. Gutierrez
  • Product ID: 701883
  • Duration: 49 Min
CD/Recorded
$395
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Recorded/CD
FDA's Proposed Rule Regarding Device Establishment Registration and Listing: Procedure on How to Register and List

FDA's Proposed Rule Regarding Device Establishment Registration and Listing: Procedure on How to Register and List

  • Speaker: David Dills
  • Product ID: 701907
  • Duration: 76 Min
Learn about the proposed Device Establishment Registration and Listing rule and how to meet the FDA requirements and expectations.
CD/Recorded
$500
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Recorded/CD
Why You Need to Integrate Your Wellness Program with Your EHS Program

Why You Need to Integrate Your Wellness Program with Your EHS Program

  • Speaker: Jonathan Klane
  • Product ID: 701902
  • Duration: 93 Min
Learn how to integrate wellness and occupational health and safety (OHS) , understand the list of areas to merge, where to start, what qualifications work, who to benchmark.
CD/Recorded
$499
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Recorded/CD
Alternative Food Preservation: Pasteurization

Alternative Food Preservation: Pasteurization

  • Speaker: Dr. Tatiana Koutchma
  • Product ID: 701886
  • Duration: 60 Min
In this Food safety training learn about Food preservation, traditional heat treatment, emerging food processing technologies, pasteurization, shelf life extension, acid and low acid foods, US FDA and USDA regulations, Health Canada, new regulatory terms and definitions, novel foods, high hydrostatic pressure, ultraviolet light, microwave heating, pulsed electric fields.
CD/Recorded
$299
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Recorded/CD
How to prepare for Increased OSHA penalties in 2011

How to prepare for Increased OSHA penalties in 2011

  • Speaker: Christopher J. Miranda
  • Product ID: 701873
  • Duration: 60 Min
CD/Recorded
$349
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Recorded/CD
Zero-Injury Workplace Culture vs. Safety Culture

Zero-Injury Workplace Culture vs. Safety Culture

  • Speaker: Joe Keenan
  • Product ID: 704986
  • Duration: 60 Min
Creating a safety culture in the workplace takes time, patience, and is often a multi-year process. This training program will examine how organizations need to transition from the existing zero injury workplace culture to a more safety oriented culture. In the process, it will examine the pros and cons behind each process and also offer best practices to determine whether you are doing it right.
CD/Recorded
$0
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Recorded/CD
Conducting A Thorough Needs Analysis and Developing A Solid Compliance Training Program

Conducting A Thorough Needs Analysis and Developing A Solid Compliance Training Program

  • Speaker: Justin Muscolino
  • Product ID: 706224
  • Duration: 60 Min
Conducting a needs analysis is important since it ultimately feeds into the creation of your compliance training program. The steps you should follow can make a big impact on the program itself and, the compliance culture. In this webinar, we will go over the necessary steps and show how it impacts your compliance training program.
CD/Recorded
$0
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