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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
Global and FDA Regulation of Electronic Cigarettes

Global and FDA Regulation of Electronic Cigarettes

  • Speaker: Azim Chowdhury
  • Product ID: 703849
  • Duration: 60 Min
The global regulatory environment for tobacco, e-cigarette and e-liquid products is rapidly evolving as legislators and regulators in the United States, European Union and Asia attempt to understand the health and safety concerns presented by these novel products, and develop appropriately tailored laws and regulations. This training course will present an overview of e-cigarette regulations in Asia, the European Union and around the world. It will also detail the key provisions of FDA’s deeming regulations.
CD/Recorded
$229
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Recorded/CD
Validation of Analytical Methods According to the New FDA Guidance

Validation of Analytical Methods According to the New FDA Guidance

  • Speaker: Dr. Ludwig Huber
  • Product ID: 703623
  • Duration: 75 Min
This webinar will elaborate the scope and content of the recent FDA guidance on validation of analytical methods. The webinar will also illustrate the lifecycle management of analytical procedures and train attendees on documentation requirements and verification of submitted methods.
CD/Recorded
$179
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Recorded/CD
Introduction to Tariff Classification: Are Your Products Classified Correctly?

Introduction to Tariff Classification: Are Your Products Classified Correctly?

  • Speaker: Reynaldo Roman
  • Product ID: 703889
  • Duration: 60 Min
This training program will discuss why the role of Harmonized System (HS) classification is crucial to the import process. The HS classification is a multipurpose, global classification tool developed and maintained by the World Customs Organization. It is used by customs agencies around the world to classify the products entering a country’s borders and forms the basis for the customs tariff of 179 countries. In fact, most countries consider the misclassification of products to be a trade violation; making tariff classification a major trade compliance issue.
CD/Recorded
$149
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Recorded/CD
Offensive Behavior and Harassment that Violates Title VII of the Civil Rights Act of 1964 - The Supervisor's Role

Offensive Behavior and Harassment that Violates Title VII of the Civil Rights Act of 1964 - The Supervisor's Role

  • Speaker: Kelly Rietow
  • Product ID: 703890
  • Duration: 60 Min
Employee complaints go with the territory when you are a manager. But how do you know when your complaints and concerns may indicate policy violations or illegal behavior? This webinar will help attendees understand the definitions of harassment and offensive behavior, protected classes, the supervisor’s role, and preventing retaliation.
CD/Recorded
$149
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Recorded/CD
Export Audit Compliance Focused Assessment

Export Audit Compliance Focused Assessment

  • Speaker: Rossano V Gerald
  • Product ID: 703881
  • Duration: 60 Min
This training program will address the export audit compliance procedures that will emphasize the appropriate documentation often used in the country market system and its product competitiveness research methods for conducting trade transactions. It will focus on identifying customers, such as the end users, distributors, and sales agents and examine the compliance procedures within foreign law justification. Finally, the webinar will address the sales documentation and other record-keeping compliance procedures that should be used by the exporter when dealing with customs for particular goods requirements for foreign business environment.
CD/Recorded
$149
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Recorded/CD
Investigating Internal Non Compliance Complaints for the General Counsel - FSLA, FMLA and USERRA

Investigating Internal Non Compliance Complaints for the General Counsel - FSLA, FMLA and USERRA

  • Speaker: Douglas Pilarski
  • Product ID: 703845
  • Duration: 120 Min
This webinar will help general counsel and senior HR executives work together to better understand internal complaint systems, and design, establish, and maintain an effective system for handling employee complaints in the workplace when associates charge that the employer has violated one or more of the laws that regulate the employer-employee relationship. The course will review three examples in this session - FSLA, FMLA, and USERRA.
CD/Recorded
$149
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Recorded/CD
Intersection of AML-OFAC Requirements with FATCA Requirements - FinCen, Customer Onboarding & More

Intersection of AML-OFAC Requirements with FATCA Requirements - FinCen, Customer Onboarding & More

  • Speaker: Steven G Lewis
  • Product ID: 703668
  • Duration: 60 Min
This session will explore the different requirements of FATCA, AML, OFAC and how to avoid breaking these regulatory requirements. You will understand how to deal with all the differing requirements and developing a Customer Due Diligence strategy to deal with such scenarios.
CD/Recorded
$149
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Recorded/CD
Health Canada’s Enforcement of the Regulatory Requirements for the Manufacture, Advertising and Sale of Pharmaceuticals, Medical Devices and Natural Health Products

Health Canada’s Enforcement of the Regulatory Requirements for the Manufacture, Advertising and Sale of Pharmaceuticals, Medical Devices and Natural Health Products

  • Speaker: Sara Zborovski
  • Product ID: 703830
  • Duration: 60 Min
The introduction of Vanessa’s Law in late 2014 has significantly changed the enforcement landscape, providing for the possibility of higher penalties than ever before in Canada. This training program will offer an overview of the new law and its potential impact on industry.
CD/Recorded
$229
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Recorded/CD
U.S. Import of FDA Regulated Products: Understanding the Entry Process

U.S. Import of FDA Regulated Products: Understanding the Entry Process

  • Speaker: Reynaldo Roman
  • Product ID: 703230
  • Duration: 60 Min
This trade webinar will explain the complex US entry process so companies that import FDA regulated products will benefit from a better understanding of how the process works. It will discuss factors and actions that can lead to an import shipment being delayed or not allowed entry into the USA.
CD/Recorded
$229
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Recorded/CD
Selection and Use of (Certified) Reference Material in Analytical Laboratories

Selection and Use of (Certified) Reference Material in Analytical Laboratories

  • Speaker: Dr. Ludwig Huber
  • Product ID: 702550
  • Duration: 75 Min
This training on using certified reference material in analytical laboratories will cover FDA and international requirements for selection, purchasing, testing, storage and use of (certified) reference material.
CD/Recorded
$179
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Recorded/CD
Managing Multiple Free Trade Agreements

Managing Multiple Free Trade Agreements

  • Speaker: Rossano V Gerald
  • Product ID: 703829
  • Duration: 60 Min
This training program will discuss appropriate import documentation, procedures for record-keeping and the U.S. customs regulations for filing and recording import documentations. It will provide import compliance materials that examine U.S. Customs and Border Protection regulations for record-keeping that can be used in the international logistic arena.
CD/Recorded
$50
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Recorded/CD
Doing Business in Canada - Canada's New Food Safety Regime

Doing Business in Canada - Canada's New Food Safety Regime

  • Speaker: Sara Zborovski
  • Product ID: 703573
  • Duration: 60 Min
This food safety webinar will provide an overview of the Safe Food for Canadians Act, and will highlight some of the key elements we are likely to see in the regulations and expected to impact imports and exports. These regulations are scheduled to be introduced in draft in the Fall, with implementation targeted for mid-2015.
CD/Recorded
$229
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Recorded/CD
How to Audit-Proof Your Physician Contracts

How to Audit-Proof Your Physician Contracts

  • Speaker: Kevin McPoyle
  • Product ID: 703226
  • Duration: 90 Min
This training on healthcare compliance will teach the attendees best practices for conducting a self audit of financial relationships with physicians. It will help you understand the key legal implications of Stark and Federal Anti-Kickback statutes.
CD/Recorded
$229
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Recorded/CD
Illegal Insider Trading: A Working Knowledge of Recent Developments

Illegal Insider Trading: A Working Knowledge of Recent Developments

  • Speaker: Aldo Martinez
  • Product ID: 703805
  • Duration: 90 Min
Although arguments exist on both sides regarding whether illegal insider trading should be deemed illegal or not, today it is globally recognized as a tool to perpetrate a fraud and is a direct threat to investors and therefore the capital raising process used by publicly traded companies. To ensure you, your employees and your financial institution are not fined, jailed or forced to close, it is imperative that you understand what to look for when identifying possible money laundering on accounts within your institution.
CD/Recorded
$149
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Recorded/CD
The EEOC Today in the New Economy - Title VII, ADEA, ADA, GINA and PDA

The EEOC Today in the New Economy - Title VII, ADEA, ADA, GINA and PDA

  • Speaker: Deirdre Kamber Todd
  • Product ID: 703827
  • Duration: 60 Min
Discrimination claims are at a historical all-time high. With claim after claim, the EEOC is busier than ever. For employers, this means that every termination, every demotion can land you in front of the EEOC. You need to know how to work within the EEOC’s system and within the new laws and regulations that the EEOC oversees.
CD/Recorded
$149
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Recorded/CD
2015 Labor and Employment Law Update

2015 Labor and Employment Law Update

  • Speaker: Diana Chomichuk
  • Product ID: 703777
  • Duration: 60 Min
Being well-trained is the first-line priority for defense in a working world where errors and omissions are costly. This course will update attendees on current labor and employment laws and help ensure better compliance.
CD/Recorded
$149
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Recorded/CD
The HIPAA Audit Program for 2015 - New Focus, New Process

The HIPAA Audit Program for 2015 - New Focus, New Process

  • Speaker: Jim Sheldon-Dean
  • Product ID: 703551
  • Duration: 90 Min
This webinar will discuss HIPAA audit and enforcement regulations and processes for 2015 and how they apply to covered entities and business associates. Attendees will learn how to prepare for HIPAA audit to avoid fines and penalties for HIPAA violations.
CD/Recorded
$149
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Recorded/CD
Deviations: What are they? Do you need to report?

Deviations: What are they? Do you need to report?

  • Speaker: Sarah Fowler Dixon
  • Product ID: 702394
  • Duration: 60 Min
This webinar will help you clearly understand, classify and determine what deviations to report in clinical studies. It will also explain, in detail, the terminology applied to deviations.
CD/Recorded
$229
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Recorded/CD
The Tools the HR Executive Needs to Build an Internal Complaint System that Gets Results!

The Tools the HR Executive Needs to Build an Internal Complaint System that Gets Results!

  • Speaker: Douglas Pilarski
  • Product ID: 703746
  • Duration: 60 Min
This webinar will help HR executives design, establish, and maintain an effective system for handling employee complaints in the workplace based on proven best practices that gets results.
CD/Recorded
$50
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Recorded/CD
FDA’s Deeming Regulation, the Continuum of Risk and Modified Risk Tobacco

FDA’s Deeming Regulation, the Continuum of Risk and Modified Risk Tobacco

  • Speaker: Azim Chowdhury
  • Product ID: 703809
  • Duration: 60 Min
This webinar will offer participants an understanding of the Tobacco Control Act, modified risk tobacco products and how FDA’s Deeming Regulation for currently unregulated products should be tailored for tobacco products depending on where they fall under the continuum of risk.
CD/Recorded
$229
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