Interest Web-based Seminars

Business Finance Training This Business Finance training course introduces students to the fundamentals of business finance. Students learn how to identify, calculate, and assess individual investments and investment portfolios, identify types of investment risks, calculate risk, and analyze the results. Students also learn how to calculate the future and present values of individual cash flows, ordinary annuities,  more...

Business Accounting Training This online business accounting training class introduces students to the fundamentals of business accounting. Students learn about current assets, long-term assets, intangible assets, and natural resources. Students also learn about the different types of liabilities, managing those liabilities, and calculating the time value of money. Course activities also cover calculating the present value,  more...

SAP FICO Online Competency Development Training program ...l cleared item reversal 10. Sample/ recurring documents/ interest calculation/ foreign currency valuation 11. Open item management/ tolerance group employees 12. Accounts Payable- Sub Ledger 13. Account group and number range creation/ document number & assign number ranges 14. Tolerance group for vendors/ Vendor master data/ Reconciliation account/ purchase invoice posting 15. payment to  more...

New Perspectives on Leadership by TrainHR Few topics in management generate as much interest as the topic of Leadership. The abiding preoccupation with this subject is reflected not only in the substantial amount of academic research whose objective is to understand the secrets of successful Leadership.  more...

The GCPICH Obligations of Sponsors Monitors and Investigators - barriers and solution - Webinar By GlobalCompliancePanel ...volved in the drug and device development process have an interest in being prepared for the audit process. Attending this Webinar is a good step toward learning the ICH processes and why the Sponsora ™s / CROa ™s Monitors are so important. Areas Covered in the Session: * The historical background of why the GCP standards were developed * The concept of and the purpose  more...

The Most Common Problems in FDA Software Validation Verification- Webinar By GlobalCompliancePanel ...ons..." The statement clearly reflects the renewed FDA interest in examining industry compliance with regulations for electronic records and electronic signatures - and its willingness to aggressively pursue enforcement actions. This FDA Software Validation and Verification (V&V) training/ webinar will review the validation planning process with particular emphasis on avoiding most common  more...

FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program - Webinar By GCP ...volved in the drug and device development process have an interest in being prepared for the audit process. Attending this Webinar is a good step toward learning the FDA processes and why the Sponsor's / CRO's Monitors are so important. Areas Covered in the Session: * What doe the FDA look at when Auditing/ Inspecting a study? * The Sponsor's responsibility in monitoring study  more...

Understanding ISO 13485 vs ISO 9001 for Successful QMS in Medical Device Industries - Webinar By GlobalCompliancePanel ...ion requirements. Why should you attend: International interest in certified quality systems is increasing. A Many foreign countries are now requesting medical device firm's supply them proof of certification to ISO 13485: 2003. To apply a CE mark under the Medical Device Directive, 93/ 42/ EEC, certification to ISO 13485 is required in most cases. This presentation is an in-depth analysis  more...

Project Management for Clinical Trials - Webinar By GlobalCompliancePanel ... * Start some initial feasibility into the countries of interest. * Ensure investigator brochure is available * Identify and decide on study management technologies and processes i. e. specific project management software to be used in the study, is the study going to use electric data capture. Areas Covered in the Session: * What is a Project and why is it important for  more...

Excel Spreadsheets and FDA Device Regulations - Webinar by GlobalCompliancePanel ...vertent and unauthorized changes. To satisfy the broadest interest, we use Excel 2003 to illustrate the tools. The seminar shifts to the regulations for automated processes, found in 21 CFR 820. 70(i), and explains the requirements for a validation plan. The FDA Guidance document, General Principles of Software Validation, has a section devoted to this kind of software application. The  more...

Know Your Customer - The DEA Due Diligence - Webinar By GlobalComplaincePanel This training will cover several recommendations to improve Due Diligence when distributing Schedules II through V controlled substances and regulated chemicals to your customers and what steps can be taken to prevent the illicit use or diversion of any product sold to a customer. As a firm handling these products, you will get a better understanding of what is required from a DEA registered  more...

ICH Q7 Guidelines and Practical Approaches to Manufacturing APIs - Webinar by GlobalCompliancePanel ... USA also played a major role in motivating international interest in the development of a "universal" API GMP. ICH Q7A Guidelines ( later renamed by ICH as Q7 ) and practical approaches will be examined during this program. All the sections contained within the issued and internationally adopted Guidance will be surveyed and discussed, as only it can be by this actual author of the approved  more...

The Most Common Problems in FDA Software Validation Verification - Webinar by GlobalCompliancePanel ...ons..." The statement clearly reflects the renewed FDA interest in examining industry compliance with regulations for electronic records and electronic signatures - and its willingness to aggressively pursue enforcement actions. This FDA Software Validation and Verification (V&V) training/ webinar will review the validation planning process with particular emphasis on avoiding most common  more...

Effective Essential CAPA process to avoid FDA 483 - Webinar by GlobalCompliancePanel ...and medical device manufacturers. It's in everyone's self interest to improve the quality of investigations and CA/ PA. This webinar will provide regulated companies the core principles and practices needed to implement an effective and efficient CA/ PA process. This presentation will begin by defining risk in compliance and the methods, which can be used to mitigate risk. One of the methods  more...

Online Excel Macros VBA Training -Get it from Home Learn writing excel macros and master the vba skills at the comfort of your home. Using online screen sharing mode with a systematical training plan acquire the necessary macro skills to automate your day-2-day excel activities. The training will give a competitive advantage to you over your colleagues. The training will be for 10 hours divided as per your interest. Payment can be done after  more...