Common Web-based Seminars

Data Integration for Data Mining with Talend Open Studio OS This course covers the many data integration procedures necessary to create a Customer Analytic Record (CAR) suitable for data mining operations. Talend OS is an Open Source tool; the client version is available for free download. The Talend company charges for the client/ server version of the tool and any support required for its installation and use. Data integration tools like Talend perform  more...

Introduction to Statistics Using Common Software Packages This course measurably increases your ability to interpret, conduct, & write comprehensive marketing reports using statistics while training using Popular Statistics software. The primary goal of the course is to be able to determine which analysis is appropriate given the question and type of data given. The course will focus on pragmatic business applications, interpretations, presentation, and  more...

Cancer in the Workplace - Best Practices and Tips for HR ...at medical issues and requests for leave of absence are a common nightmare for HR. Moreover, recent statistics suggest that cancer is one of the most debilitating illnesses that workers have. Yet many employees are able to continue working while receiving treatment. According to the EEOC, more than one million Americans are diagnosed with some form of cancer each year and aapproximately 40  more...

Learning to work as a Team This team buiding training course teaches students how to be effective team members. Students learn how to communicate effectively, adapt to various personality styles, overcome common problems, work on aspects of verbal and nonverbal communication, create a supportive team environment, understand the source of team conflict, and employ different conflict resolution styles. Course activities also  more...

MOC 6460 - Visual Studio 2008: Windows Presentation Foundation Training This WPF training class provides students with the knowledge and skills to build and configure a Windows Presentation Foundation (WPF) solution. The class is intended for application developers who know how to build Windows Forms applications, custom user controls in .NET Framework 2.0 and how to use the common features of the base class library.  more...

MOC 6461 - Visual Studio 2008: Windows Communication Foundation Training This WCF Training class provides students with the knowledge and skills to build and configure a Windows Communication Foundation (WCF) solution. This WCF class targets application developers who know how to build and consume Web services in Microsoft .NET Framework and how to use the common features of the base class library.  more...

Comprehensive JSP Training ...stom tag libraries that establish a portable standard for common processing tasks in JSP. JSTL is a major part of the new scriptless authoring style encouraged (and enabled) by the JSP 2.0 specification. This module covers all four JSTL libraries in depth: The core actions, which support JSP expressions for JSP 1.x containers, flow control for procedural processing in JSPs, and  more...

Java Swing Training ...table building simple or complex interfaces with the most common Swing controls and classes -- including buttons, lists, combo boxes, checkboxes and radio buttons, text controls, trees, and tables -- controlling multiple windows and dialogs, using panes to manage related interfaces, implementing popup menus, and using data transfer packages for clipboard and drag-and-drop implementations. The  more...

Administration of JBoss Application Server V4 Training This JBoss administration training class teaches the basics of the deployment and administration of web applications to a JBoss Application Server V4 environment. on Windows. This course concentrates on providing best-practice solutions to handle common problems that occur in a JBoss environment so students will have a high-level of skill with regard to JBoss administration.  more...

Intermediate and Advanced Microsoft Excel 2003 Training In this Microsoft Excel 2003 training course, you will learn to streamline and enhance your spreadsheets with templates, charts, graphics, and formulas.This course was designed for students who need the skills necessary to create templates, sort and filter data, import and export data, analyze data, and work with Excel on the Web. In this advanced Microsoft Excel 2003 training course, you will  more...

Intermediate and Advanced Excel 2007 Training This Microsoft Excel training course is designed for students with some experience working with Microsoft Excel 2007. You will learn to apply visual elements and advanced formulas to a worksheet to display data in various formats. In addition, you will automate some common Excel tasks, apply advanced analysis techniques to more complex data sets, collaborate on worksheets with others, and  more...

Business Ethics Training ...ituations arise. Course activities also cover identifying common managerial ethical issues, being proactive with ethical issues, addressing subordinates ' ethical issues, identifying causes of unethical behavior, recognizing unethical behavior, and ending unethical behavior in the workplace. Students will also learn about organizational ethical principles, and the four categories of corporate  more...

SharePoint 2007 Governance Training This SharePoint training course covers the ins and outs of governance in general as well as common taxonomies. You will review what a Governance plan is made up of, as well as learn how to create a training plan, SharePoint service offerings and how to follow through with enforcing the plans. We will review Information Architecture and why it is important.We will take a look at each level in  more...

Advanced Microsoft Access 2003 Training ...d queries, forms, and reports; writing macros to automate common tasks; and performing general database maintenance. It is also designed as one in a series of courses for students pursuing the Microsoft Office Specialist Certification for Microsoft Office Access 2003. Students will learn introductory level administrator skills. This advanced Access course is also for the student who may be  more...

Advanced Microsoft Excel 2003 Training ...rosoft Excel 2003 training course, you will automate some common Excel tasks, apply advanced analysis techniques to more complex data sets, collaborate on worksheets with others, and share Excel data with other applications.This course was designed for students desiring to gain the skills necessary to create macros, collaborate with others, audit and analyze worksheet data, create PivotTables  more...

Advanced Microsoft Excel 2007 Training In this advanced Microsoft Excel 2007 training course, you will automate some common Excel tasks, apply advanced analysis techniques to more complex data sets, collaborate on worksheets with others, and share Excel data with other applications.  more...

MOC 6418 - Deploying Windows Server 2008 This Windows Server 2008 training class provides students with an understanding of migrating and deploying Windows Server 2008 including installation, configuration, and upgrading. Special emphasis is given to upgrading common server configurations and using the Microsoft Deployment Toolkit.This class is intended for IT professionals who are experienced with Windows Server 2000 or Windows Server  more...

Six Strategies to Grow Aggressively in the Federal Market webinar on June 14th 2012 ...there. Can you relate to any of the following problems commonly reported by small businesses? a Lack of a clear strategy to take the company to the next level of growth where the revenue comes at a consistently increasing rate. a Majority of business comes from subcontracting to others. a Bidding only on a handful of proposals a year, and having a low win rate to boot. a Lack of  more...

Implementing Statistical process Control SPC for Short Run Production ...ion operations. Application of SPC techniques have become commonplace and a normally accepted business practicea accept in make-to-order short-run production environments. This is because SPC techniques are usually taught within the context of high volume continuous process operations where it is normally easy to acquire a statistically significant sample of a measurement population. But  more...

The Most Important Metrics For Measuring Supply Chain Performance ... my organization to focus on what is TRULY important?a Common supply chain metrics observed in many manufacturing companies include: a Inventory Turns or Days-of-Supplya metrics that describe the efficiency or inventory and use of working capital. a Cycle Timea the elapsed time to complete an activity or a set of activities. Common cycle time metrics include: a Customer  more...

Demystifying the Calculations of Efficiency Utilization and Productivity ...rrect) use of the term gets lost. When this happens, the common language we use in business to communicate with each other breaks down. So it is with the manufacturing industrya ™s standard terms; efficiency, utilization and productivity. These terms, though each having distinctly different meanings with distinctly different consequences, are often incorrectly interchanged especialy  more...

FDA Requirements for Device Labeling Development Contents Distribution and Changes - Webinar GlobalComplianceP Overview: Marketing wants to entice customers to buy your product instead of your competitor's! A common method is to make the labeling as eye-catching as possible. Wednesday, May 16, 2012 10: 00 AM PDT | 01: 00 PM EDT  more...

Medical Device Supplier Quality Agreements - Webinar By GlobalCompliancePanel Overview: The FDAa ™s Quality System Regulation (QSR) explains how a device manufacturer must manage suppliers. This ranges from supplier evaluation and selection to control methods. One common approach uses a supplier quality agreement. This webinar explains the elements of a supplier quality agreement and its implementation. Wednesday, June 20, 2012 10: 00 AM PDT | 01: 00 PM EDT  more...

510k Submissions Requirements Challenges and Successful Clearance - Webinar By GlobalCompliancePanel Overview: A premarket notification [510(k)] submission is the most common pathway to market for medical devices including in vitro diagnostic devices. Thursday, April 19, 2012 10: 00 AM PDT | 01: 00 PM EDT  more...

Avoiding an FDA Warning Letter with a Strong CAPA Program - Webinar By GlobalCompliancePanel Overview: The development and implementation of an effective CAPA system is not well understood by many device companies. This webinar is designed to clarify what the FDA is looking for in the CAPA system. Examples of warning letters will be reviewed to understand common themes found by FDA. Thursday, March 29, 2012 10: 00 AM PDT | 01: 00 PM EDT  more...

FDAs 21 CFR 11 Add-On Inspections - Recent Updates - Webinar By GlobalCompliancePanel This presentation will cover the scope, status and results of the surveillance inspections and what they may mean for the future of 21 CFR Part 11. This will enable you to determine whether your company is subject to the most common violations so you can take action to have a better inspection outcome. Tuesday, February 14, 2012 10: 00 AM PST | 01: 00 PM EST  more...

Calculating Overtime Correctly - Webinar By TrainHR ...ion covers proper procedures for calculating overtime and common pitfalls involved in the process. The importance of being thorough and correct when calculating regular rate of pay to avoid massive Department of Labor penalties is also highlighted as well as its importance in avoidance of suffering damages from civil law suits. Why you should attend: Calculating overtime is simple, right?  more...

HIPAA Compliance and Patient Care Where the Challenges are - Webinar By mentorhealth Dona ™t miss the opportunity to identify common privacy violations that make substantive critical difference in the safety of patients, staff, and families. Safety and privacy are partners in that if patients withhold information due to distrust in their information being confidential. Thursday, October 20, 2011 10: 00 AM PDT | 01: 00 PM EDT  more...

Practical Laboratory Statistics This presentation will attempt to remove the fear of statistics that most people share. We will not spend much time on complex equations. Rather, we will focus on the concepts of statistics, and how you can use these concepts to interpret your laboratory results. Our focus will be on using basic spreadsheet functions to compare data sets generated from many different kinds of test equipment.  more...

HIPAA and Security Breaches Most frequent issues and causes and trends for future threats by GCP The HIPAA Breach Notification Rule has been in effect since September 23, 2009 and most organizations are not prepared to respond to a breach of PHI and report and document it properly. We will discuss the origins of the rule and how it works, including interactions with other HIPAA rules and penalties for violations  more...

Root Cause Analysis and Documentation Requirements for CAPA - Webinar By GlobalCompliancePanel RCA is a popular topic and many companies realize its importance in correcting problems. However, there is still much confusion and many problems continue to recur. This webinar will use thoughtful discussion, humorous analogies and case studies to distinguish between the true root cause and other common imposters. Emphasis will be placed on realizing system interactions and cultural  more...

The 510k Submission Requirements Contents and Options - Webinar by GlobalCompliancePanel Overview: This presentation will provide an understanding of how to get a device requiring a 510(k) submission to market quickly. Knowing when and how to properly submit a 510(k) for a device or change to a device is critical to a company's regulatory and financial health. Your goal is to get the 510(k) through the review process as quickly as possible. This presentation will also distinguish  more...

Designing a CAPA System that Meets and Exceeds Regulatory Requirements - Webinar By GlobalCompliancePanel Overview: CAPA is the most audited Quality subsystem in any Quality system. Most of the warning letters written by the FDA in 2010 were CAPA relate. Avoiding FDA CAPA findings starts with the design of a robust CAPA SYSTEM. The webinar covers "Off-label statute" and the FDA's nonbinding off-label guidance as relates to re-prints, performance claims, and Promotion. Emphasis is placed on ethical,  more...

The Most Common Problems in FDA Software Validation Verification- Webinar By GlobalCompliancePanel ...lanning process with particular emphasis on avoiding most common pitfalls. Software V&V is an extremely important requirement for ensuring the safety and reliability of software used in manufacturing, devices, design, and quality systems. FDA has cited numerous companies on software verification and validation issues in Warning Letters and inspectional observations. The presentation will  more...

Understanding Attribute Acceptance Sampling including Z14 and c0 Plans -- Webinar By GlobalCompliancePanel ...ables to determine the sampling plan * Ways to avoid common errors and misunderstandings with the sampling tables * The difference between single, double, and multiple sampling plans * Why double sampling plans are the most economical choice * The reasons for the switching rules between normal, reduced, and tightened * The use of the switching rules to help improve your  more...

Calibration and Qualification in Analytical Laboratories - Webinar By GlobalCompliancePanel ...equirements for calibration and qualification * Most common inspection problems * USP Chapter : Analytical Instrument Qualification * Development of an effective equipment qualification master plan * Calibration/ qualification phases: design qualification, installation qualification, operational qualification, performance qualification * Allocating equipment to  more...

The Use and Mis-use of FMEA in Medical Device Risk Management - Webinar By GlobalCompliancePanel ...er and benefits of FMEA for your organization by avoiding common pitfalls and concentrating efforts toward the real value of the FMEA process. Areas Covered in the Session: * What is an FMEA o What are the components of an FMEA? * How should I use FMEA in performing risk management? * What are the problems with FMEA in risk management? * How is an FMEA  more...

Purchasing and Supplier Controls in the Medical Device Industry - Webinar By GlobalCompliancePanel ... efficient, equally compliant options to many of the most common practices. Why you should attend: A lack of adequate control over purchases has resulted in a significant number of recalls due to component failures. Since FDA cannot regulate component suppliers, it is imperative that your company's purchasing and supplier control requirements provide the assurance that only acceptable  more...

Preparing for Pre-approval Inspections - Webinar By GlobalCompliancePanel ...n process will be reviewed followed by a detailed look at common focus area areas of Inspectors. Procedures to be followed after the inspection such as preparation of the response to 483s will be discussed. Ample discussion time will be available at the halfway point in the webinar and again at the end of the webinar. Why you should attend: Pre-approval inspections provides a relatively  more...

Best practices for conducting OOS investigations - Webinar By GlobalCompliancePanel ...e steps and the order in which they are to be performed. Common pitfalls and means of overcoming them at each of the steps will be identified by a review of recent Warning Letters. The structure of an Investigation report which satisfactorily documents the investigation will be discussed. Ample time will be available for Q&A halfway through the webinar and at the end. Why you should attend:  more...

XML Training ...OURSE OVERVIEW Audience for this course Common uses of XML Other technologies with XML Gain by learning XML 2. INTRODUCTION TO XML What is XML Sample XML The W3C XML & HTML Advantage of XML Where is XML used? Show the Demo from Google/ Amazon Webservices 3. USING XML IN APPLICATIONS Separates Data Simplifies Data Sharing Simplifies Data  more...

Process Validation current industry practices and FDA Guidance Document Review - Webinar by GlobalCompliancePanel Overview: Process Validation is required by FDA and most regulatory bodies. PV demonstrates consistency of pharmaceutical processes. PV requires writing and executing a validation protocol that explores either natural variation or introduced variation in a process and shows that the process can consistently produce a quality product. Writing and executing good process validation can be a  more...

Practical Laboratory Statistics - Webinar by GlobalCompliancePanel ...and complicated equations. We use real world examples and common spreadsheet functions to show you how to analyze your data. Areas Covered in the Seminar: * Perspectives on statistics * Basic definitions * Hypothesis testing * Evaluating differences in precision - the F Test * Evaluating differences in averages - the t Test * Evaluating real world data sets  more...

21 CFR Part 11 Complete Manual For Compliance Success - GlobalCompliancePanel Virtual Seminar - Webinar By GlobalCompliancePanel ...in scope or the scope of the inspection o Some commonly asked questions by the inspectors and benefits of being compliant * Module 3 - Internal and External Auditing for Part 11 Compliance o Aspects of auditing for Part 11 compliance- starting at the audit program level and then going down on how to prepare for an audit to how to successfully execute the audit and  more...

Labeling Requirements for Dietary Supplements - Webinar By GlobalCompliancePanel ...mpanies. The webinar teaches the attendee how to avoid common labeling compliance issues including: * Misbranding * Misleading claims * Misleading statements * Directions of use The webinar focuses on general labeling provisions for dietary supplements, requirements for inner and outer packaging, and claims made on e-commerce websites. Why should you attend:  more...

Validating Excel and Word Applications Documents - Webinar By GlobalCompliancePanel ...e increasing user benefits. How does this translate to common software applications programs, e. g., MS-Excel and MS-Word, or similar. How can these be verified and validated? Company quality data must be more "science based". What V&V (verification and validation) planning steps are expected under the CGMPs and other guidance documents for such apps software? How can these consistently be  more...

Project Management in a cGMP Environment - Webinar By GlobalCompliancePanel ...ring a planned documented rationale. Three of the most common tools will be discussed. One very simple approach using common Excel- or Word-type PC applications programs that can be used immediately. Regular use of a few simple but powerful tools will virtually eliminate "fire fighting" in a new project. Regular use can contribute greatly to reduction of scheduling uncertainty, incomplete  more...

Preparing for GFSI and other Third Party Audits - Webinar By GlobalCompliancePanel Overview: Preparation and organization are the keys to a successful audit. This session will allow your team to anticipate the auditors needs and result in the facility's ability to achieve the maximum benefit and score from the audit. Why you should attend: More and more customers are requiring GFSI audits such as ISO 22000, BRC and SQF or accepting them in lieu of their own audits.  more...

Why is CAPA so often cited in medical device inspections - Webinar By GlobalCompliancePanel Overview: This presentation will explore FDA Corrective Action and Preventive Action findings in medical device manufacturer quality systems to determine FDA's concerns. The FDA and ISO 13485 requirements for CAPA will be reviewed to identify how procedures may define a compliant CAPA system. Implementation and maintenance of the CAPA system will be explored. FDA indicates that CAPA systems  more...

Medical Device Reporting Regulations and Violations - Webinar By GlobalCompliancePanel ... will review the Medical Device Reporting regulations and common violations leading to Warning Letter filings by FDA. As part of the review, actual Warning Letter and FDA-483 citations of small and large medical device manufacturers will be explored for Medical Device Reporting issues. There is a great deal of concern at FDA over the quality of the information being reported and the  more...

Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences - Part I and Part II - Webinar By GlobalCompli ...llustrate effective compliance procedures and techniques. Common issues which have caused difficulties for Life Sciences firms will also be discussed. Course content will also explain how Japan interacts with and utilizes ICH standards and how they relate with other national regulatory agencies. The course will also discuss how personnel can best address the conflicts that sometimes arise and  more...

How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant - Webinar By GlobalCompliancePane ...d: Protocol Deviations and Violations are one of the most common problems identified by FDA Investigators and is a main reason for the rejection of clinical data from a particular site or even a study. Forewarned is forearmed. Areas Covered in the Session: * How to know when the protocol is not followed (PNF)? * What is the difference between a protocol deviation and a violation?  more...

Root Cause Analysis Shutting Down the Alligator Farm - Webinar by GlobalCompliancePanel RCA is a popular topic and many companies realize its importance in correcting problems. However, there is still much confusion and many problems continue to recur. This webinar will use thoughtful discussion, humorous analogies and case studies to distinguish between the true root cause and other common imposters. Emphasis will be placed on realizing system interactions and cultural  more...

The Most Common Problems in FDA Software Validation Verification - Webinar by GlobalCompliancePanel ...lanning process with particular emphasis on avoiding most common pitfalls. Software V&V is an extremely important requirement for ensuring the safety and reliability of software used in manufacturing, devices, design, and quality systems. FDA has cited numerous companies on software verification and validation issues in Warning Letters and inspectional observations. The presentation will  more...

Supplier Evaluation and Assessment How to Meet FDA QSR and ISO 13485 Requirements in a Cost-Effective Manner - Webinar by Global Supplier qualification and assessment is required in both the QSR regulations and ISO standards. Many companies spend a great deal of time and money in pursuit of compliance with this. Many companies can spend MUCH LESS time and money, and still be in control of their suppliers and in compliance with the regulations. This presentation will review the QSR and ISO requirements for supplier  more...

Project Management for FDA-Regulated Companies - Webinar by GlobalCompliancePanel ...f of "progress against plan", and ot Three of the most common tools will be discussed. One very simple approach using common Excel- or Word-type PC applications programs that can be used immediately. Regular use of a few simple but powerful tools will virtually eliminate "fire fighting" in a new project. Regular use can contribute greatly to reduction of scheduling uncertainty, incomplete  more...

Robust Process Validation for Medical Devices - Webinar by GlobalCompliancePanel ...common reasons noted by the FDA for recalls of medical device is improper validation. It is also one of the most common reasons companies receive 483s and warning letters. Conversely, successful validations not only satisfy compliance and regulatory requirements, they also provide for robust manufacturing processes satisfying the needs of many individual functions within your organization  more...