![](/images/products/large/705550.jpg)
Successfully Negotiating The Labor Agreement
Gerry McLaughlin
90 Min
Product Id: 705550
In this webinar attendees will learn how to select the right management team and also understand the union team, to handle union pressure tactics, to come to an agreement.
![](/images/products/large/706058.jpg)
Technical Writing in an Industrial Environment
Robert Peoples
60 Min
Product Id: 706058
Attend this webinar to learn the logical, fast and simple process of how to easily write any document that your company requires. Explore how to organize collected information, write the document and address the comments from reviewers and approvers.
![](/images/products/large/703258.jpg)
How to Survive CBP Free Trade Agreement Verification
Donna L Shira
60 Min
Product Id: 703258
This U.S. Customs & Border Protection (CBP) compliance training will provide attendees tools to ensure they comply with rules and regulations applicable to Free Trade Agreement (FTA) and special trade program claims.
![](/images/products/large/705585.jpg)
Biocompatibility Testing; what you need to know
Mike Colvin
90 Min
Product Id: 705585
This Webinar is geared toward those who require a working knowledge of biocompatibility.
![](/images/products/large/706168.jpg)
Regulatory and Testing Requirements of Bacterial Endotoxin Testing (BET) using LAL
Carl Patterson
60 Min
Product Id: 706168
cGMP drug products rely on the bacterial endotoxin test as a critical release test for products based on the route of administration of the drug product. Having a good concept of this critical release assay, its application and importance to the manufacture of cGMP product is valuable as to avoid costly errors, batch disposal, expensive failure investigations and delays in the release of products that some manufacturers have undergone.
![](/images/products/large/706167.jpg)
Say what you do; Do what you say; and Prove it! Quality Management System Essentials
Susanne Manz
90 Min
Product Id: 706167
This webinar will help you to establish a Quality Management System (QMS) for Medical Device Companies. A well-structured QMS meets the requirements of the Quality System Regulations and is both effective and efficient. The regulations require that manufacturers “establish and maintain a quality system that is appropriate for the specific medical device(s) designed and manufactured”. In order to “establish” a suitable and effective QMS, medical device companies must be able to “say what they do, do what they say, and prove it”!
![](/images/products/large/703319.jpg)
How to Prepare a Customs Compliance Manual
Donna L Shira
60 Min
Product Id: 703319
This webinar will explain how to prepare a Customs manual that complies with CBP laws and regulations. Attendees will learn best practices for successfully passing an audit or becoming an Importer Self Assessment Program (ISA) member.
![](/images/products/large/706133.jpg)
Management of the Data Safety Management Committee for Clinical Trials
Yashar Salek
60 Min
Product Id: 706133
Join this webinar to receive instructions on the uses of, need for, setup of, and management of a Data Safety Management Committee for an FDA regulated clinical trial.
![](/images/products/large/706145.jpg)
How To Roll Out A POC Molecular Diagnostic
Todd Graham
60 Min
Product Id: 706145
Attend this webinar to learn about the considerations which must be kept in mind before performing PCR in the Point of care format. This webinar will make sure that healthcare facilities know what is necessary to perform these tests in a simple, yet powerful manner.
![](/images/products/large/704975.jpg)
HIPAA Planning for 2020 and Beyond - Protecting Patient Information Privacy and Security
Jim Sheldon-Dean
90 Min
Product Id: 704975
This HIPAA compliance webinar will discuss the issues in patient information privacy and security that healthcare organizations will face in 2020 and how to ensure compliance with HIPAA that will withstand incidents, audits, and investigations by HHS.
![](/images/products/large/706109.jpg)
3-hr Virtual Seminar: Coding Evaluation and Management Services to Survive an Audit
Carol Hoppe
3 hrs
Product Id: 706109
This webinar will help physicians and non-physician practitioners document efficiently and to effectively support evaluation and management (E/M) codes to survive a payer audit.
![](/images/products/large/704316.jpg)
CDISC Mapping 5: ADAM Models - ADSL, BDS and ADAE
Sunil Gupta
90 Min
Product Id: 704316
This training session is intended for anyone directly or indirectly responsible for the creation, content or validation of CDISC data sets, tables, and data lists used to support research, drug or medical device efficacy and safety in a regulatory submission. The program will provide effective and practical solutions to address real-world issues.
![](/images/products/large/706102.jpg)
Comparability Protocols For Approved Drugs
Peggy Berry
90 Min
Product Id: 706102
This webinar will address approaches to developing comparability protocols, including primary content considerations and timing of submission. The information obtained will enable completion of appropriate testing to make changes to the drug substance or drug product formulation, manufacturing facility, and container closure which can be designed to save time and money in the future.
![](/images/products/large/705218.jpg)
Understanding Appraisals and Appraisal Review Concepts for Lenders
Heidi Lee
90 Min
Product Id: 705218
This webinar training will break down common terms used in the appraisal industry as well as cover the economics of real estate markets: the impact of the principles of value, the forces of value, and real estate market life cycles.
![](/images/products/large/703211.jpg)
Risk Management of Source Water used in the Food Industry
Michael Brodsky
60 Min
Product Id: 703211
This training on source water protection will address the issue of source water protection and the potential impact on the food industry. Attendees will learn the best practices for the protection of source water and risk management from a microbiological perspective.
![](/images/products/large/705089.jpg)
Child Support and Garnishments - All You Need To Know
David Sanders
90 Min
Product Id: 705089
This webinar will enhance your knowledge by helping you understand the basics of garnishments, liens and levies, how to identify and define their various types, and how to calculate them. This webinar training will help you better understand the various techniques used by your company.
![](/images/products/large/706166.jpg)
The Transfer of Validated Methods
John Fetzer
60 Min
Product Id: 706166
This webinar will discuss the best practices of the transfer of validated methods including statistics of analytical methods, how to define universal methods, how to make the method operation uniform, training issues, and the use of transferring methods.
![](/images/products/large/705833.jpg)
2019 New Privacy Officer Training - Module 2
Nanette Awad
75 Min
Product Id: 705833
HIPAA Privacy Officer Training will provide a comprehensive overview of all ongoing activities of a Privacy Program related to the development, implementation, maintenance of, and adherence to the organization’s policies and procedures covering the privacy of, and access to, patient health information in compliance with federal and state laws and the healthcare organization’s information privacy practices.
![](/images/products/large/706160.jpg)
Developing Quality Objectives And Strategy for An Efficient And Effective QMS
Susanne Manz
90 Min
Product Id: 706160
This webinar will help you to develop strategy and objectives for an effective and efficient Quality Management System (QMS) for Medical Device Companies. A suitable and effective Quality Management System requires a thoughtful and methodical approach to create and execute. This webinar will help medical devices companies understand their current state and strategy for improvement. If you’ve had serious quality issues, compliance problems, or are dealing with the costs of an inefficient QMS, this webinar is for you.
![](/images/products/large/701407.jpg)
Avoid Documentation 'Time Bombs'
John E Lincoln
60 Min
Product Id: 701407
This documentation training will explain regulatory ramification of communication done through Lab books, SOPs, DHF, technical files etc and how to reduce it.