Quality Control for Microbiological Media and Reagents
Todd Graham
60 Min
Product Id: 705060
This webinar will give you the tools you need to maintain a quality supply of media and reagents in a variety of microbiology laboratories. A thorough understanding of the variety of challenges necessary in maintain quality media and reagents will be brought to the fore. This will allow you to perform microbiology testing with confidence.
ISO 45001: Mitigation Essentials - Part 2
Michael Aust
60 Min
Product Id: 705076
This second training program in the series will review the structure of ISO 45001. It will discuss the mitigation process for the standard, the terminology associated with it, and its key requirements.
Performing an Effective Out-of-Specification Result Investigation
Charity Ogunsanya
90 Min
Product Id: 705064
This webinar will provide the basic understanding of how to conduct a compliant and effective out-of-specification (OOS) result investigation which is critical in preventing product recalls, voluntary and involuntary plant shut down, and FDA 483 findings or warning letter. It will also provide a basic mainframe for the Quality Assurance unit in the final disposition of the affected finished product as well as provide guidance for the different types of OOS investigational systems.
Subcontractor auditing (cGMP/Pharma/Med device industries)
Jan Warner
90 Min
Product Id: 705063
This course will describe the basic principles and requirements for building a supplier audit program. This webinar will provide a framework on which to build your subcontractor auditing program.
Interview Questions and Pre-Employment Screening What Every Employer Needs to Know - Title VII, ADA/ADAAA, PDL, GINA, I-9s and Affirmative Action
Janette Levey Frisch
120 Min
Product Id: 703948
This training program will offer an overview of anti-discrimination laws and affirmative action issued for federal contractors; illegal and ill-advised interview questions; pre-employment tests (skills, strength, medical tests) use of social media, criminal background checks; and more.
Packaging and Labeling for Commercial and Clinical Products
Peggy Berry
90 Min
Product Id: 704378
This training program will discuss optimizing your packaging design for commercial and clinical products and translating a protocol into effective packaging design. Attendees will learn how to implement an effective artwork change management system. Real-life case studies and dos/don’ts for packaging and labeling for commercial and clinical products will also be discussed.
NYS Department of Labor Proposed Salary Increases
Matthew W Burr
60 Min
Product Id: 705071
With the overtime changes in New York State, this training program will discuss areas in New York State where the change will take effect. It will also discuss future changes to the rate and potential federal changes to the overtime rule.
Confined Space Rules for Construction as per OSHA Final Rule
Michael Aust
60 Min
Product Id: 705069
In this interactive training session, attendees will obtain the latest and newest OSHA regulatory information and how it effects confined spaces at you construction site. The course will also help provide practical advice on how to implement practice contractor ‘vetting’ for hiring the best employees for your organization.
Corporate Governance and the Board of Directors' Role
Adam Kerns
60 Min
Product Id: 705067
This webinar will offer a comprehensive, in-depth review of the state laws affecting the corporate governance standards applicable to insurance companies and the board of directors’ role in those standards.
Strategies to Conduct a Successful Method Transfer according to FDA Expectations
Kim Huynh-Ba
90 Min
Product Id: 705059
This webinar discusses how to execute meaningful Method Transfers by selecting appropriate analytical performance characteristics and acceptance criteria, documentation of the transfer process and how to avoid failures.
Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations
Rachelle D Souza
60 Min
Product Id: 704906
This webinar will discuss FDA’s current recommendations on using electronic health records in prospective clinical investigations of human drugs, biologics, medical devices and combination products.
Effective Discipline and Lawsuit-Proof Termination: How to Remedy Performance and Conduct Problems While Minimizing Your Legal Risks
Susan Fahey Desmond
90 Min
Product Id: 705058
This training program will elucidate effective documentation techniques. It will discuss what documentation is needed to justify a termination decision and key record retention requirements. Attendees will learn how to fill out a performance appraisal and understand the essentials of a document retention program.
Implementing a Modern Pharmaceutical Quality System
Steven Laurenz
60 Min
Product Id: 705055
This presentation explores the basic concepts making up an ICH Q10 Quality System approach and steps to properly implement the concepts.
Business Email Compromise and Ransomware - Red Flags and Mitigation
Rayleen M Pirnie
60 Min
Product Id: 705038
The Internet Crime Complaint Center (IC3) reports that U.S. victims alone lost $18 million in 15 months to just a single form of ransomware. This training program will review the risks associated with various types of cyber fraud, and in particular, business email compromise (BEC) and ransomware. The session will also discuss documenting sound business practices to minimize exposure and loss and list what to present to your board of directors before an incident.
Importing into the United States in Compliance with U.S. Customs & Border Protection (CBP)
Jennifer Diaz
60 Min
Product Id: 702212
This U.S. Customs & Border Protection (CBP) compliance training will help you understand best practices when importing products into the U.S.
Overview of Penalties for Different OSHA Violations in 2017
Michael Aust
60 Min
Product Id: 704965
This training program addresses the increase in OSHA penalties. The new penalties took effect August 2, 2016. Any citations issued by OSHA on or after this date will be subject to the new penalties if the related violations occurred after November 2, 2015.
Introduction to Country of Origin
Randi Waltuck Barnett
90 Min
Product Id: 704193
This training program will discuss the historical background, legal framework, and overall concepts of origin. It will also highlight the difference between non-preferential and preferential origin and guide attendees in making origin determinations for imports and exports.
US Controls on Exports Abroad and Re-Exports: Understand the Regulatory and Administrative Concerns
Matilda Vasquez
60 Min
Product Id: 705010
This training program will offer an overview of the Foreign Trade Regulations, the 10 General Prohibitions of the Export Administration Regulations, Office of Foreign Assets Controls and the International Traffic in Arms Regulations. It will also offer insight into exports abroad, transshipment and re-export regulations and practices.
US Export Filing Requirements and the Proper Use of EAR 99
Grant Smith
60 Min
Product Id: 705004
Exports are governed by the Bureau of Industry and Security (BIS), under the US Department of Commerce. Exports are regulated by the type of export, the value of the export, and the destination of the export. These factors will help determine the documents needed, and the filings needed to legally export. This webinar training will cover US export filing requirements and the proper use of EAR 99. Failure to follow requirements can result in costly customs holds and or fines/penalties.
AML Risks in Correspondent Banking: What You Need to Know for 2017
Joe Soniat
60 Min
Product Id: 704997
Correspondent banking has become a hot topic with BSA AML over the past few years. With examination scrutiny on correspondent banking high, this training program will highlight why it is essential to know the risk and what to do when it comes to banking other banks.







