Categories Web-based Seminars

Business Ethics Training This Business Ethics training course introduces students to the fundamentals of business ethics. Students learn about the decision-making process to solve ethical dilemmas, understanding barriers and consequences when making ethical decisions, and the process for blowing the whistle when unethical situations arise. Course activities also cover identifying common managerial ethical issues, being  more...

How to Factually Evaluate Critical Supplier Performance and Risks Manufacturers and distributors are choosing to source significant amounts of materials and components from global suppliers and are creating substantial risks within their supply chains. Companies are discovering that sourced-material disruptions can and often do, result in dramatic and unfavorable impacts to material delivery reliability, total material cost and received material quality.  more...

How to Calculate the Impact on Total Factory Costs from a One Percent Change in Planned Load ... are included in variable, semi-fixed and fixed cost categories overcoming myths of accounting for variable costs. a How to differentiate escapable from non-escapable costs the role variable margin plays in product focused decision making. a How to take the incremental fixed cost reductions to enterprise valuation. Won't you join us for this FREE webinar on  more...

Adverse Event Reporting for Dietary Supplements and OTC Drugs - Webinar By GlobalCompliancePanel Since passage of the Dietary Supplement & Nonprescription Drug Consumer Protection Act in Dec. 2007, FDA requires reporting of serious adverse events for dietary supplements and OTC drugs. Manufacturers and importers of products in these categories often have questions about what constitutes a serious adverse event and about Adverse Event reporting requirements that this Webinar will be able to  more...

Calibration and Qualification in Analytical Laboratories - Webinar By GlobalCompliancePanel ...nt o Allocating Analytical Instruments to USP Categories * Allocating Analytical Instruments to USP Categories Areas Covered in the Session: * Operational lab equipment requirements for calibration and qualification * Most common inspection problems * USP Chapter : Analytical Instrument Qualification * Development of an effective equipment  more...

HIPAA Business Associates How the regulations have changed and what you need to do for compliance now - Webinar By GCPanel ...nforcement penalties * Learn about the new violation categories * Learn about being prepared for a HIPAA Compliance Audit Agenda: * Old Ways, New Ways - Changes to the Rules o Origins of Changes to Business Associate Rules o New Definitions of Business Associates o Contractors of Business Associates * New Requirements and Changed  more...

HIPAA Breach Notification What to do to prevent breaches and what to do when they happen to you - Webinar By GCPanel Overview: The new HIPAA Breach Notification Rule required by the HITECH Act within the American Recovery and Reinvestment Act of 2009 went into effect September 23, 2009, requiring all HIPAA covered entities and business associates to follow a number of steps to be in compliance. * The HIPAA Breach Notification Rule has been in effect since September 23, 2009 and most organizations are not  more...

Medical Device Recalls How to Manage Them and Recent Trends - Webinar By GlobalCompliancePanel ...n place. FDA classifies medical device recalls into three categories, representing the potential risk to public health: Class I, II, and III. Areas Covered In the Seminar: * Create and use a recall operational procedure and what should it contain * Understand what are effectiveness checks * What happens in a medical device recall and your responsibility * Learn why a  more...

Introduction to Operational Risk - Webinar By GlobalCompliancePanel ... will be able to: PART ONE * Identify the major categories of Risk according to Basel * List the seven major categories, 20 categories, and 40 subcategories of operational risk * What to look for in taking a holistic and systematic approach to op risk * Comprehend the major qualitative and quantitative tools used in op risk * Understand how self assessments,  more...

Medical Device Classification - Webinar by GlobalCompliancePanel ...found in Annex IX of the MDD. Devices fall into four risk categories (I, IIa, IIb, and III). The risk class of the device determines the available conformity paths the manufacturer may use to affix the CE mark. This webinar explains the risk classification and conformity paths using the MDD version in effect after March 2010. The Canadian Medical Device Regulations (CMDR) classifies devices  more...

Managing Product Medical Device Recall Efficiently and Effectively - Webinar by GlobalCompliancePanel Recall means the correction or removal of a device for human use where FDA finds that there is a reasonable probability that the device would cause serious, adverse health consequences or death. It is an action taken to address a problem with a medical device that violates FDA law. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective  more...

Update on Unique Device Identifier for Device Manufacturers FDA is reconsidering whether some form of unique device identification (UDI) is warranted for medical devices, given the potential of UDI to help reduce medical errors, facilitate recalls, and other issues identified from above but also improve inventory control, improve reimbursement, and reduce product counterfeiting. Once your device is approved, ongoing regulatory requirements fall largely  more...

GETIIT Business Objects Business Objects is the primary supported query tool used to provide access to the Data Warehouse. Business Objects presents the data in three hierarchical collections or categories: universes, classes, and objects. You will be learning in this program how to develop and deploy the universe and objects using Business Objects.  more...