
Quality Planning Process and Procedure
Ronald Schoengold
60 Min
Product Id: 700665
This Quality Planning training/webinar will define the Quality policy and plan with the help of procedure, Manual and templates where manufacturer decides how to apply these regulatory guidelines in developing a plan that consistently delivers high quality products and services.
Overview of the Harmonized Tariff Schedule of the United States - Classifying Your Products for Customs Purposes
Paula Connelly
60 Min
Product Id: 700659
This Harmonized Tariff Schedule of the United States training/webinar will provide an overview of the structure of the HTSUS and how to use the HTSUS to determine the correct classification, duty rate, and possible quotas, restrictions or preferential duty rates that may be applicable to your product.

Sarbanes-Oxley, IT and Segregation of Duties
George Spafford
60 Min
Product Id: 700112
This segregation of duties (SOD) training/webinar in Sarbanes-Oxley and IT will provide an overview of the current interpretation of Sarbanes-Oxley and will talk about what risks that Sarbanes-Oxley is especially concerned with when it comes to segregation of duties.

Interviewing and Hiring in Compliance with Federal and State Laws
Marna Hayden
60 Min
Product Id: 700647
The HR Compliance training/webinar in Interviewing and Hiring will cover various interviewing techniques and the processes used to make effective selection decisions.

Validation of Potency Bioassays for Biologicals
Ana Menendez
60 Min
Product Id: 700201
This Validation of Potency Bioassays training/webinar for Biologicals provides logical approaches that should be implemented during early development to increase predictability and deliver rugged, compliant assays through Phase III and commercialization.

Overall Residual Risk and Risk Acceptability for Medical Devices
Edwin L Bills
60 Min
Product Id: 700622
This Residual Risk and Risk Acceptability webinar/training in medical devices will discuss how to meet this requirement and also how to determine what disclosures of risk need to be made in the instructions for use of the medical device and Proper evaluation of overall residual risk and the acceptability of this risk.

FDA's cGMPs for the 21st Century Initiative
Betty Jones
60 Min
Product Id: 700620
This FDA’s cGMPs training/webinar will provide and insider’s view FDA’s path to restructuring its regulatory oversight of manufacturing quality that is based on quality systems and risk management approaches.

AML requirements for non-bank financial institutions
Kenneth Barden
60 Min
Product Id: 700483
This webinar will focus on AML issues relevant to non-bank financial institutions, such as insurance companies, capital market intermediaries, pension funds, etc.

The FDA's Outlook for Quality in Device Manufacturing
James Harris(PhD)
60 Min
Product Id: 700645
This Device Manufacturing webinar provide a understanding of the GMP and Quality requirements for the design, manufacture, storage, distribution, and installation of Medical Devices including the requirements for complaint handling, and servicing.
The New Dietary Supplement Good Manufacturing Practices
John Suzuki
60 Min
Product Id: 700642
This New Dietary supplements webinar will highlight from a quality perspective the introductory requirements of these new CGMP regulations and examine methods and strategies for meeting these new requirements.
Producing Results in a Too-Much-to-Do World: Productivity and Time Management for the 21st Century
Matthew W Burr
60 Min
Product Id: 700640
In this Productivity and Time Management webinar/training you will learn some great new thinking in productivity management.

Failure Modes and Effects Analysis (FMEA) - An Effective Tool for Risk Management
Vinny Sastri
60 Min
Product Id: 700537
This Failure Modes and Effects Analysis (FMEA) Webinar will give an overview and elements of an FMEA. The analysis of data outputs will also be discussed.

Part 11 - Electronic Records and Electronic Signatures
Betty Jones
60 Min
Product Id: 700619
This Part 11 - Electronic Records webinar will provide an insider’s view FDA’s current thinking regarding the scope and application of Part 11 of Title 21 of the Code of Federal Regulations; Electronic Records; Electronic Signatures (21 CFR Part 11).

Introduction to statistical Design and Analysis of Experiments (DOE)
Lawrence Mucha
60 Min
Product Id: 700344
This statistical Design and Analysis of Experiments webinar will introduce DOE and process modeling.

Designing Regulatory - Compliant Clinical Research Data Management Systems
Dale Hunscher
60 Min
Product Id: 700562
This presentation covers the fundamental principles underlying the various compliance regulations and discusses their implications for system designers and integrators.

Risk Management - Beyond the Numbers
Roger Greenwald
60 Min
Product Id: 700624
This Risk Management webinar/training will describe enhancements to these techniques that can improve your relationships with customers and regulatory agencies, resulting in a reduced number of surprises during inspections.

Doing Business under the North American Free Trade Agreement, Understanding NAFTA
David Ross
60 Min
Product Id: 700496
This NAFTA webinar/training is designed for middle and upper management to help them understand these complex rules to avoid costly fines and penalties and delays in moving their products within North America.

How to Prepare for FDA Compliance
Betty Jones
60 Min
Product Id: 700618
This FDA compliance webinar provides FDA’s current thinking on modernizing the regulation of quality and manufacturing science through establishment of a new regulatory framework.
OSHA 300 Recordkeeping: How To Do It Right!
David Stumbo
60 Min
Product Id: 700576
This OSHA webinar will review the requirements for OSHA 300 record keeping, including the basic tenants of coverage, recording criteria, forms, and postings.

Global Terms of Sale: Understanding Incoterms 2000
David Ross
60 Min
Product Id: 700495
This module is designed for middle and upper management to help them understand the complexities and the financial impact on their international business