10 CAM Mistakes and How to Avoid Them
Robert Machson
60 Min
Product Id: 704308
This training program will list common CAM mistakes and practical solutions that will save you money. If you are the owner or operator of leased property, a tenant, franchisee, attorney, paralegal, lease administrator or auditor, you want to make sure that you are not paying more than you ought to.
How to Spot a Potentially Violent Worker in the Workplace: Protect Your Workforce
Vanessa G Nelson
60 Min
Product Id: 704374
This training program on reducing and preventing workplace violence hazards will train attendees on spotting a potentially violent worker in the workplace. It will also enumerate OSHA requirements regarding violence in the workplace and discuss employer’s responsibilities and industry trends for workplace violence.
Accounts Receivable - Collection Techniques
Brian Shanahan
90 Min
Product Id: 704279
This training program will help attendees discover the importance of segmenting accounts based on size and payment behavior and then using the right collection technique with the right customers. The course will also offer an understanding of the best practices that should be deployed around each of these collection techniques.
FDA Inspection Lessons Learned: Lack of Trial Oversight
Janet Ellen Holwell
90 Min
Product Id: 704263
This training program will critically assess the number of major and critical 2012 inspection findings related to trial oversight. Attendees will learn to identify regulatory requirements for appropriate delegation of duties and investigator oversight.
Regulation V - Fair Credit Reporting Act
Kara Lamphere
60 Min
Product Id: 704290
This webinar will discuss the Regulation V – Fair Credit Reporting Act(FCRA) in details and explain attendees what types of marketing are allowed, requirements of affiliate marketing, and disclosures required with regard to consumer credit report. Speaker will discuss about consumer credit report alerts and identity theft protections, as well as what an institution must do with these alerts.
California and Federal Requirements for Paid Sick Leave - Conflicts and Jurisdiction
Cathleen M. Hampton
90 Min
Product Id: 704363
This training program will provide an overview of the key intent for establishing paid sick leave programs and policies. It will also discuss the finer points of California law and how that relates to trends spotted all across America.
Using Analysis of Variance - A Practical Approach
Daniel O Leary
60 Min
Product Id: 703824
This training program will illustrate the underlying idea that makes ANOVA work. It will also offer an understanding of the data collection issues you should plan and how to get access to ANOVA in Excel.
How to Properly Monitor Process and Performance of Pharmaceutical Solid Dosage Equipment
Michael Levin
60 Min
Product Id: 704274
Among other key topics, this training program will focus on what can be monitored in mixing operations, wet granulation operations, dry granulation operations, compaction operations, and coating operations.
Preparing for FDA's Unique Device Identification Rule
Daniel O Leary
90 Min
Product Id: 702594
This 90-minute webinar will review FDA's draft regulations for UDI and describe the new requirements for labeling medical devices. It covers the new regulations in 21 CFR Part 830, the changes to Part 820, the Quality System Regulation; Part 801, Labeling; Part 803, Medical Device Reporting; Part 806 Corrections and Removals; and other regulations.
Making Sense of BSCs, Hoods, Isolators, RABs
Joseph Winslow
60 Min
Product Id: 704361
Attendees will come away from the training program with the tools they need to understand the various types of enclosures and how to select the correct type of enclosure for their process in order to meet regulations, protect the product, and ensure worker safety. The course is apt for personnel in FDA regulated industries who want to learn about what enclosure is best suited for their process and why.
Title 19 Customs Duties Parts 200 to End, Revised
Suzanne Richer
60 Min
Product Id: 704357
This training program will analyze the customs entry process and AD/CVD (Antidumping and Countervailing). It will also clarify reimbursement statements – what they are and how they work and regulations on AD/CBP/CVD.
Out in the Open: Protecting Your Privacy and Identity in the Digital Age on the Internet
Joseph Rosner
60 Min
Product Id: 704256
This privacy protection in the digital age training program will detail what the Internet of Things is and how it collects data and tracks you. It will further examine the risks attached to personal information and more.
CDISC Mapping Webinar Series: Comprehensive Training Package (5 Courses)
Sunil Gupta
7.25 hrs
Product Id: 704358
This comprehensive training program will discuss CDISC requirements to create SDTMs and ADaMs. It will also offer essential mapping and strategy concepts for creating and validating SDTM and ADaM variables in key CDISC datasets (DM, AE, ADSL, and ADAE).
Complimentary Webinar: Introduction to Managing Multiple Compliance Efforts Leveraging Common Controls
Craig Isaacs
60 Min
Product Id: 704123
This webinar is the compliance professional’s guide for a better, more efficient way to jumpstart their GRC strategy and manage compliance. If you feel like you are drowning in a sea of regulations that gets worse every day, learning how to harmonize those government and industry regulations will ease that stress.
Vendor Management - Building a Strong Questionnaire
Michael D King
60 Min
Product Id: 704119
This training program will highlight why a vendor questionnaire is the keystone your vendor management program is built on. The course will help ensure attendees get the whole picture and determine appropriate controls for information security and privacy.
ISO/IEC 27001:2013 - Breaking It Down to Understand and Implement
Michael C Redmond
90 Min
Product Id: 703977
This training program will guide attendees in implementing and complying with the requirements of ISO 27001:2013. ISO 27001 is an international standard published by the International Standardization Organization (ISO), and it describes how to manage information security in a company. The latest revision of this standard was published in 2013, and its full title now is ISO/IEC 27001:2013.
Employee Discharge and Documentation: Using Documentation to Control the Employment Relationship
Douglas Pilarski
120 Min
Product Id: 704036
This webinar will help managers establish best practices for managing their workforce using sound performance management techniques, especially documentation of poor job performance and code of conduct violations to best support terminations. Learn how HR can coach their executives and managers on how best to work through their performance management strategy.
Veterinary Drug Approval Process and FDA's Regulatory Oversight
Karl M. Nobert
60 Min
Product Id: 703971
This training program will provide attendees with an introduction to FDA’s veterinary drug approval process. It will also discuss key components of an appropriate animal field study needed to support new animal drug approval and explain how jurisdiction is split between various federal agencies in certain cases.
Be Ready for eMDR Going Live August 14, 2015
Rita Hoffman
110 Min
Product Id: 703972
This training program will discuss the basics of the Medical Device Reporting (MDR) regulation and review the process for preparing and submitting Electronic Medical Device Reports (eMDRs).
The Sunshine Act Reporting for Clinical Trials
Mukesh Kumar
60 Min
Product Id: 703883
This webinar will discuss the disclosure requirements for clinical investigators under the Sunshine Act. It will discuss the details of the processes; provide templates for reporting formats; and timelines for reporting.







