ComplianceOnline

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.

Recorded/CD
Writing an Investigative Case Report | Findings and Recommendations

Writing an Investigative Case Report | Findings and Recommendations

  • Speaker: John E Grimes
  • Product ID: 704837
  • Duration: 90 Min
This training program will discuss how to synthesize an abundance of investigative information into a concise, thorough, accurate, and unbiased report. It will also offer pointers on creating an easy to read, professional looking document. Attendees will learn to effectively organize case reports.
CD/Recorded
$199
Recorded/CD
Creating and Maintaining an Effective and Efficient Technical Training Programs

Creating and Maintaining an Effective and Efficient Technical Training Programs

  • Speaker: Ginette M Collazo
  • Product ID: 704373
  • Duration: 90 Min
This training program will analyze key elements of training programs in regulated environment. It will also list key performance indicators related to training and offer best practices for developing technical training programs to improve their effectiveness.
CD/Recorded
$249
Recorded/CD
Exporting to Canada Procedures and Documentation

Exporting to Canada Procedures and Documentation

  • Speaker: Jan Seal
  • Product ID: 703136
  • Duration: 90 Min
This training on export compliance will help you understand documentation and procedures to assist in expediting clearance of commercial goods through Canada Border Services Agency.
CD/Recorded
$149
Recorded/CD
TSCA Awareness Program for 2017

TSCA Awareness Program for 2017

  • Speaker: Joe Keenan
  • Product ID: 705251
  • Duration: 90 Min
This training program will clearly define all requirements of the Toxic Substance Control Act (TSCA). It will discuss best practices for developing TSCA written plans and TSCA training plans, as well as breakdown all components of the TSCA.
CD/Recorded
$199
Recorded/CD
AML Compliance and FinCEN Updates and its Implications

AML Compliance and FinCEN Updates and its Implications

  • Speaker: Armen Khachadourian
  • Product ID: 705185
  • Duration: 90 Min
The webinar will provide an overview of the currency and monetary reporting requirements imposed by the Bank Secrecy Act. It will also discuss red flags that pose present and future challenges for regulated businesses. Recognizing and investigating suspicious activities is the key in safeguarding an organization's financial system from illicit use and combating money laundering. Timely and accurate reporting will promote national security through the collection, analysis, and dissemination of financial intelligence to the proper authorities.
CD/Recorded
$0
Recorded/CD
Overhauling Outdated Credit Decisioning: Understanding and Best Practices

Overhauling Outdated Credit Decisioning: Understanding and Best Practices

  • Speaker: David Peterson
  • Product ID: 705187
  • Duration: 60 Min
In this training program, attendees will learn the 9 regulations governing payments risk and KYC/KYCC in which you may be out of compliance, as part of the process to overhaul outdated credit decisioning.
CD/Recorded
$0
Recorded/CD
Marketing and Advertising Compliance - The First UDAAP Hotspot

Marketing and Advertising Compliance - The First UDAAP Hotspot

  • Speaker: Kara Lamphere
  • Product ID: 703451
  • Duration: 90 Min
This webinar will explain Unfair, Deceptive, and Abusive Act or Practices (UDAAP), including different standards for advertising over the internet and social media. It will also provide practical solutions for avoiding the pitfalls and still create meaningful advertisements.
CD/Recorded
$249
Recorded/CD
Preventing and Detecting Fraudulent Vendor Disbursements

Preventing and Detecting Fraudulent Vendor Disbursements

  • Speaker: John E Grimes
  • Product ID: 704505
  • Duration: 90 Min
This training program will highlight various disbursement fraud schemes. It will also discuss preventing disbursement fraud by establishing a strong anti-fraud policy and understanding of the human factor.
CD/Recorded
$149
Recorded/CD
How Create a Value-added cGMP/ISO 13485 Internal/Supplier Auditing System

How Create a Value-added cGMP/ISO 13485 Internal/Supplier Auditing System

  • Speaker: Betty Lane
  • Product ID: 705165
  • Duration: 60 Min
This webinar will cover creating of a value-added an internal and supplier auditing program for compliance to FDA and ISO 13485 internal auditing requirements. It will include how to set up and manage the auditing system, as well as how to conduct audits, and document the results and any nonconformities. It will discuss the value of a good auditing program.
CD/Recorded
$0
Recorded/CD
Monitoring and Measuring Customer Satisfaction Using ISO 10004:2012

Monitoring and Measuring Customer Satisfaction Using ISO 10004:2012

  • Speaker: Daniel O Leary
  • Product ID: 703752
  • Duration: 90 Min
Medical device manufacturers need systems to implement regulatory requirements (meeting customer requirements and handling regulatory complaints) as well as a business processes to determine customer satisfaction. While the three systems are related, each serves a different purpose. You will learn how to implement a customer satisfaction process to complete theses three important aspects.
CD/Recorded
$0
Recorded/CD
Introduction to EU REACH for US Manufacturers

Introduction to EU REACH for US Manufacturers

  • Speaker: Jim Kandler
  • Product ID: 705190
  • Duration: 60 Min
EU REACH can be confusing and many in the US seek a more solid understanding of it. In this introductory webinar, participants will be introduced to the important terms and concepts of the directive. They will obtain a basic knowledge of what RoHS is about and if they need to learn more.
CD/Recorded
$179
Recorded/CD
What You Should Know About Export Requirements for FDA Regulated Products from US to Foreign Countries

What You Should Know About Export Requirements for FDA Regulated Products from US to Foreign Countries

  • Speaker: Rossano V Gerald
  • Product ID: 705186
  • Duration: 60 Min
When exporting outside the U.S., exporters must consider the Food and Drug Administration (FDA) provisions as it helps them understand what documents and procedures are needed in coordination with the transaction process. This training program will provide an in-depth explanation of FDA-regulated products that are exported from the United States to foreign countries. Also, it will address what export documentation must be used in the transportation of FDA-regulated products.
CD/Recorded
$0
Recorded/CD
Virtual Seminar: Regulatory Modernization in Canada and the US: An Overview of the Key Elements

Virtual Seminar: Regulatory Modernization in Canada and the US: An Overview of the Key Elements

  • Speaker: Felix Amiri
  • Product ID: 705182
  • Duration: 2.5 hrs
This 2.5 hours training will review the key elements of the new food regulations in Canada, the United States and the international marketplace. Get accustomed to new regulatory expectations and be prepared to develop relevant and productive compliance plans.
CD/Recorded
$0
Recorded/CD
GMP Training Practices to ensure Regulatory Compliance

GMP Training Practices to ensure Regulatory Compliance

  • Speaker: Henry Urbach
  • Product ID: 705077
  • Duration: 90 Min
By attending this webinar, you will gain a better understanding of the regulatory expectations for an effective and GMP-compliant training system. In this webinar your instructor will share with you what he has learned over the past decade of developing and delivering effective GMP training programs as well as from his 25 plus years of working in the Life Science industries.
CD/Recorded
$0
Recorded/CD
Comply With OFAC: Cuba Sanctions Regulations

Comply With OFAC: Cuba Sanctions Regulations

  • Speaker: Shaun Miller
  • Product ID: 705101
  • Duration: 90 Min
This training will review Office of Foreign Assets Control (OFAC) and the US Department of Commerce, Bureau of Industry and Security (BIS) respectively amended; the Cuban Assets Control Regulations (CACR) and the Export Administration Regulations (EAR) to further ease the US embargo against Cuba and authorize certain business activities with Cuba in targeted sectors.
CD/Recorded
$199
Recorded/CD
Evaluating, Selecting, and Contracting for Compensation/Payroll/HR (HRIS)/Benefits/Consultants/Software

Evaluating, Selecting, and Contracting for Compensation/Payroll/HR (HRIS)/Benefits/Consultants/Software

  • Speaker: Rob J Thurston
  • Product ID: 705166
  • Duration: 60 Min
This training program will take a closer at human resources administration and benefits administration. It will help attendees evaluate and find quality services, determine whether Software as a Service (SAAS), cloud-based or onsite implementation is best for your needs, and detail best practices to do a cost-benefit analysis.
CD/Recorded
$0
Recorded/CD
MDR Program conforming to New FDA Guidance

MDR Program conforming to New FDA Guidance

  • Speaker: Edwin Waldbusser
  • Product ID: 705149
  • Duration: 60 Min
FDA, in November 2016, issued a Guidance explaining and clarifying the existing MDR regulation. Many of the details of the MDR regulation were unclear and ambiguous and resulted in nonconformances. This new Guidance attempts to eliminate confusion.
CD/Recorded
$249
Recorded/CD
Affordable Care Act (ACA); Discrimination; Interpreter and More: Complying with Section 1557: OCR and CMS Hospital CoPs

Affordable Care Act (ACA); Discrimination; Interpreter and More: Complying with Section 1557: OCR and CMS Hospital CoPs

  • Speaker: Sue Dill Calloway
  • Product ID: 705151
  • Duration: 120 Min
Section 1557 of the Affordable Care Act (ACA) forbids discrimination based on sex, race, color, national origin, age and disability. It builds on longstanding and familiar federal civil rights laws but is the first law to prohibit discrimination on the basis of sex (which includes gender, gender identity and sex stereotyping) in covered health programs and activities. Sex discrimination also includes discriminatory treatment on the basis of pregnancy, false pregnancy, termination of pregnancy, recovering from pregnancy, childbirth and related medical conditions, sex stereotyping, and gender identity.
CD/Recorded
$0
Recorded/CD
Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based Approach

Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based Approach

  • Speaker: Joy McElroy
  • Product ID: 704306
  • Duration: 90 Min
This 90-minute training program is designed for people tasked with performing external audits for their organizations. It is also for those tasked with developing, maintaining and/or improving programs for manufacturing facilities. This includes individuals that have quality management system responsibilities for making general improvements in their organization’s performance specifically related to equipment, processes and documentation.
CD/Recorded
$169
Recorded/CD
OSHA 101 - Nuts and Bolts of a Safer Workplace

OSHA 101 - Nuts and Bolts of a Safer Workplace

  • Speaker: Michael Aust
  • Product ID: 705099
  • Duration: 60 Min
This training program will illustrate five effective personal actions to enhance a safer workplace and describe the four different phases of the safety maturity curve. It will explain the four most common deflections of a safe workplace and how to minimize their impact.
CD/Recorded
$0
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