> > > >

Describe Web-based Seminars

Describe Training Provider? - Tell us about your Training!

Matching Training Programs

online course

instructor-led class

learn at home

group study

self-directed study

cd-based training

DVD video training

printed book

e-book digital book

workshop seminar

train the trainer

computer-based learning

discount pricing

online tutorial

Describe Training Seminars and Classes

From Performance Innovation LLC

Lean Overview Course Description: Companies responding to cost pressures understand how lean principles and techniques can improve operations, reduce costs and increase profit margins. Lean is about creating value for customers by eliminating waste Course Objectives: By the end of the course participants will be able to: 1. Identify the eight forms of waste. 2. Describe the value of 5S and Visual more...

From Certified Foreclosure Agent Program

FREE Short Sale Fundamentals 101

...e list of adjectives that real estate agents often use to describe the short sale process is almost always anything but "short." The good news is times are changing. There are numerous ways in which you can cut the time in half, get your offers pushed to the top of the stack and do very well with short sales. All it takes is the inside knowledge of how to coordinate these deals properly to get more...

From Requirements Solutions Group

How to Package and Communicate Business Requirements

...iness, stakeholder, solution, and transition requirements describe what information technology has to deliver but making sure that both parties agree on just what these requirements mean is the real challenge. This virtual workshop presents concepts, tools, techniques, and ideas for packaging, presenting, and communicating these types of requirements to both the business and technology more...

From Manufacturing Executive Institute

The Most Important Metrics For Measuring Supply Chain Performance ...: 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 Order Promised Cycle Time a Customer Order Actual Cycle Time a Manufacturing Cycle Time a Purchase Order Cycle Time 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...

Demystifying the Calculations of Efficiency Utilization and Productivity ... these three terms, demonstrate how to calculate each and describe where they are used in a manufacturing enterprise. With the demonstration of the formulas, we will explain how values derived from the formulas can be altered and how companies can benefit from the CORRECT understand of these terms. We will clearly show participants HOW to calculate these values and WHEN to use the results of more...

From GlobalCompliancePanel

GMP for Phase 1 Products - Webinar By GlobalCompliancePanel Overview: This presentation will cover the contents of the guidance that was given. FDA has issued as rule that relieves Phase 1 products from complying with the GMP given in 21 CFR 211. At the same time, they ruled that the products must continue to comply with the GMP as given in the Food, Drug, and Cosmetic Act. Guidance was then given to describe these GMP. Tuesday, August 7, 2012 10: 00 more...

Excel Spreadsheet Validation for FDA 21 CFR Part 11 - GlobalCompliancePanel ...describe the regulatory and business requirements for Excel spreadsheets, using examples from FDA recommendations. It will then cover the design and installation of those Excel Spreadsheets, to ensure the integrity of the data, and will discuss how to ensure 21 CFR 11 compliance during the development, installation and maintenance of a spreadsheet application. Thursday, June 14, 2012 10: more...

Business Process Optimization in Pharmacovigilance - Webinar By GlobalCompliancePanel ...describe how to assess and optimize Pharmacovigilance operations from cost effective, compliance, and safety perspectives. A structured methodology for assessing drug safety operations will be presented. This will include recognizing the need to conduct process analysis, developing and prioritizing project portfolio, performing the analysis, and finally implementing the findings. Thursday, more...

Excel Spreadsheet Validation for FDA 21 CFR Part 11 - Webinar By GlobalCompliancePanel ...describe the regulatory and business requirements for Excel spreadsheets, using examples from FDA recommendations. It will then cover the design and installation of those Excel Spreadsheets, to ensure the integrity of the data, and will discuss how to ensure 21 CFR 11 compliance during the development, installation and maintenance of a spreadsheet application. Tuesday, January 24, 2012 more...

New Process Validation Life-Cycle Approach - Apply statistical tools to demonstrate Process Capability - Webinar By GlobalCompli This webinar will describe the new Process Validation Life-Cycle Approach as defined in the revised FDA guideline. The three stages will be described in detail including: Process Design, Process Qualification and the Continued Process Verification. Thursday, December 15, 2011 10: 00 AM PST | 01: 00 PM EST more...

Preventing Harassment in the Workplace by TrainHR ...rses employees have. It will define who is covered and describe the two main kinds of sexual harassment in the workplace. It will cover what should be in an effective Harassment policy, how it should be communicated, and who is held responsible for assuring compliance. Also included is handling complaints, documenting charges and conduct and addressing any situation that may be construed as 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...

Master Production Record Requirements - Webinar By GlobalCompliancePanel This program will address the 21CFR and Eudralex Volume 4 requirements and interpretation, as well as FDA Guidance regarding the creation, review and approval, and control of Master Production Records. The material will enable attendees to establish a consistent approach to the design of MPR, including cover page content, instructions, processing requirements and limits, and signature more...

Good Documentation Practices for Laboratory Operations - Webinar By GlobalCompliancePanel ...facturing and support areas. Good Documentation Practices describe the required activities and steps to use when recording data and other handwritten entries. Personnel, who work with documentation must be informed of these requirements, recognize their significance to their job and be aware of the consequences of non-compliance. During this webinar, you will review agency and industry standard more...

Internal 21CFR Part 11 Compliance Auditing of Computer Systems - Webinar By GlobalCompliancePanel ...facturing, testing and systems. This presentation will describe a proven process for preparing a site for inspection of systems. Case studies will be used to illustrate how this process has successfully prepared several pharmaceutical companies to answer this question accurately, completely and to the great satisfaction of the inspectors. We will review and illustrate audit plans, system more...

Requirements of the Master Production Record - Webinar By GlobalCompliancePanel ...d handling of Batch Production Records (BPR), and clearly describe the difference between the master and the batch production record. Why should you attend: All the requirements for the master production record (MPR) are based on relevant US and EU regulations. Failure to recognize and implement those requirements can have devastating effects on your company's quality system, including more...

Good Documentation Practices for GMP Operations - Webinar By GlobalCompliancePanel ...facturing and support areas. Good Documentation Practices describe the required activities and steps to use when recording data and other handwritten entries. Personnel who work with documentation must be informed of these requirements, recognize their significance to their job and be aware of the consequences of non-compliance. During this 1-hour webinar, we will review the Good Documentation more...

The Pharmaceutical Quality System - Webinar By GlobalCompliancePanel ...This webinar will discuss the evolution of the standards, describe a Pharmaceutical Quality System and discuss the transition to the Pharmaceutical Quality System. Why you should attend: The US FDA, and regulatory agencies around the world, are actively promoting the concept of a Pharmaceutical Quality System. The concept of a Quality System was imposed on the medical device industry through more...

Elements of the Lot Disposition Process - Webinar By GlobalCompliancePanel ...product, and in-house manufactured components. It will describe a well-defined Quality role, identify requirements for resources, and outline the expectations for documentation review. Additionally, the course will look at the creation of disposition packages for approval and rejection of materials, and cover changes in disposition status. The course will not cover the disposition of raw more...

Medical Device Reporting Regulations and Violations - Webinar By GlobalCompliancePanel ...ivities including the status of the electronic system and describe the upcoming requirements for manufacturer reporting. Why should you attend: Medical device manufacturers continue to have problems with the MDR regulations and reporting of potential adverse events and possible device malfunctions. The regulation has been unchanged for several years, but FDA continues to find violations of more...

Webinar on Pharmacovigilance Audit - Webinar by GlobalCompliancePanel ...describe how to conduct a thorough drug safety and pharmacovigilance audit, including compliance with applicable worldwide laws, regulations and guidance. In addition, attendees will learn how to compare the company's pharmacovigilance operations to applicable best practices. The course will cover all aspects of drug safety and pharmacovigilance compliance including the collection, more...

European Drug Safety and Pharmacovigilance Compliance - Webinar by GlobalCompliancePanel This webinar will describe European PV requirements, including compliance with applicable laws, regulations and guidance. In addition, attendees will learn how to compare the company's PV operations to applicable best practices in Europe. more...

Defining and Managing Protocol DeviationViolationException - Webinar by GlobalCompliancePanel ... CFR or other regulatory rules. The various terms used to describe PNF (violation, deviation, and exception) are open to different interpretations by the parties involved. Attend this Webinar to understand the proactive approach to define and manage Protocol Deviation/ Violation/ Exception. What is the approach to predict and prevent it. Proper documentation and reporting of PNF as they more...

Signal Detection and Case Processing Business Process Optimization in Pharmacovigilance - Webinar by GlobalCompliancePanel ...describe how to assess and optimize pharmacovigilance operations from cost effective, compliance, and safety perspectives. A structured methodology for assessing drug safety operations will be presented. This will include recognizing the need to conduct process analysis, developing and prioritizing project portfolio, performing the analysis, and finally implementing the findings. The more...

From Clinical Solutions Medical Training

Assisting With Medication Certification Course ...s and some age related route and form considerations. 3. Describe how medicine indications, contraindications, interactions, side effects, adverse reactions, dosages, proper storage and disposal as well as the components of a complete label and a complete MD order impact on assisting with medicines. 4. Recognize acceptable abbreviations and their meanings. 5. List and apply the 7 "rights of more...

Palliative Care and End of Life Certification Course ...tion presented here, you will be able to: *Describe physical and psychosocial issues associated with dying patients *Identify the Physical changes which may occur during the stages of death. *Identify the role of Hospice in dealing with the dying patient. *Identify the role of Palliative care in a dying patient. *Identify the role of pain management *Understand more...

Pediatric and Adult Moderate Sedation ...arance between moderate sedation and deep sedation. 4. Describe complications and high risk factors of sedation. 5. Discuss the indications for and the goals of sedation in children. 6. Define pre-procedure, intra-procedure, and post-procedure assessment parameters. 7. Define the ASA classification system. 8. Discuss methods of drug administration and specific agents. 9. List 3 more...

Alzheimers Certification Course ...s the signs and symptoms associated with Alzheimer's 4. Describe the Stages of Alzheimer's 5. Identify the diagnostic tests involved with the process of the disease Please visit our website at www. clinicalsolutionsme. com to sign up for this online class. Class includes study guide and test. If you have further questions you can reach us at 1-877-243-8885. Take courses online. more...

HIPAA Course ... the information presented here, you will be able to: *Describe the intent of HIPAA *Describe various professional practices that protect patients' privacy *Discuss practices that protect security of electronic protected health information Please visit our website at www. clinicalsolutionsme. com to sign up for this online class. Class includes study guide and test. If you more...

HIV AIDS Course ...iscuss the epidemiology and transmission modes of HIV 2. Describe population at risk and how it is spread 3. Describe prevention methods and behavioral changes 4. Pass the written test with a score of at least 80% Please visit our website at www. clinicalsolutionsme. com to sign up for this online class. Class includes study guide and test. If you have further questions you can reach more...

From InfoStar International

PeopleSoft PeopleTools Upgrade and Data Management Rel 850 ...t using the Oracle database platform. Learn To: * Describe the PeopleSoft databases and how they are created * Describe the role of PeopleTools in PeopleSoft applications and design/ construct a PeopleTools implementation * Explain PeopleSoft Pure Internet Architecture and the implications for system design and implementation * Install PeopleSoft components on a web more...

From Keen Info Solution

SAP ABAP Online Training ECC 60 ...ete, Free, Exit, Continue, Stop, Describe) * Control Break Statements and Include Programs 7 Modularization Techniques * Over view of Modularization * Includes * Subroutines * Function Modules 8 Data Dictionary * Creation of Data Base Table (Transparent, Pooled and clustered tables) * Buffering, Indexes etc., more...

Online Training for SAP ABAP ECC 60 with 6y Real Time Expert ...P (Clear, Refresh, Delete, Free, Exit, Continue, Stop, Describe) * Control Break Statements and Include Programs 7 Modularization Techniques * Over view of Modularization * Includes * Subroutines * Function Modules 8 Data Dictionary * Creation of Data Base Table ( Transparent, Pooled and clustered tables) * Buffering, Indexes etc. * Creation of Domains * Creation of more...

Online Training for Oracle SCM R12 with 6y Real Time Expert ... Management Process Inventory Organizations and Items Describe Enterprise Structure in Oracle Applications Defining Units of Measure Defining Locations Setting up Inventory Organizations Establishing Inventory Parameters Defining Sub-inventories Item Attributes Creating an Item Enter Orders Entering Simple Negotiation information Entering Sales Header and Line information more...

From Hrd200 Consulting Group, Llc

Assertiveness and Self-Confidence training ...nfidence, and list the four styles of communication a Describe the types of negative thinking, and how one can overcome negative thoughts a Explain the difference between listening and hearing, and understand the importance of body language and questioning skills in communication a Define the importance of goal setting, and practice setting SMART goals for assertive behavior a more...