Preparation Web-based Seminars

Live Online PMP Preparation Training from PMSoft Live Online PMP Preparation Training from PMSoft scheduled on 17th Sept. 2011  more...

Data Mining for CRM using STATISTICA Data Miner ...y the Recipes interface, which automates much of the data preparation, as well as the modeling functions of the tool. Finally, the unique availability of the Tweedie mathematical distribution is introduced for use with General Linear Models (GLMs) for modeling insurance risk related to frequency and severity of loss. Tweedie offers an intermediate exponential probability distribution between  more...

SAP FICO Online Competency Development Training program ...ct Costing- Basics Attendees also learn: 1. Resume Preparation Guidelines and Tips 2. Mock Interviews and Interview Preparation Tips should Here are some videos explaining how we conduct our training program, use Training Blogs and Google documents to communicate with our trainees and share the Assignments, Video Recordings, Training documents, Training materials for our training  more...

JAVA J2EE JEE Professional Role Based Training from Zaran Tech ...Web Services 4. SOA Attendees also learn: 1. Resume Preparation Guidelines and Tips 2. Mock Interviews and Interview Preparation Tips should attend? Following professionals should plan on joining: a Entry-level IT a Non IT professionals aspiring to get into J2EE/ JEE. a Self-taught IT J2EE/ JEE wanting to fill in the gaps and put all the pieces together a Systems  more...

SAP BOBJ with BW integration Online Competency Development Training program ...tification Guidelines Attendees also Learn: 1. Resume Preparation Guidelines and Tips 2. Mock Interviews and Interview Preparation Tips Here are some videos explaining how we conduct our training program, use Training Blogs and Google documents to communicate with our trainees and share the Assignments, Video Recordings, Training documents, Training materials for our training program,  more...

Business Analyst Competency Development Program ...oject Experience a High Quality Materials a Resume Preparation Guidance a Mock Interviews a FREE On Job Support for 3-4 months The Business Analyst Training uses best practices and guidelines from International Institute of Business Analysis (IIBA ®) in their Business Analysis Body of Knowledge ® (BABOK ® v2. 0). The training content is customized to meet the  more...

FDA Inspections - Dos Donts The purpose of the FDA inspection is a verification activity that should demonstrate to the regulatory agency and provide assurance that products consistently meet quality expectations and that your company is operating in a consistent and compliant state of control.  more...

Auditing an Active Pharmaceutical Ingredient API Contract Manufacturing Organization CMO - Webinar By GlobalCompliancePanel ... * Examine key elements of an API audit * Audit preparation * The audit itself o Opening Session o Audit itself o What to look for? o Discussion of findings o Suggestions and experience * Closing Meeting * Who should participate in audit * Who should attend openning and closing sessions * Audit Reports  more...

Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine ... This Webinar is designed for people involved in document preparation and maintenance, and those who have involvement with documentation. The FDA QSR and the Medical Device Directive specify certain documents or records that should be included in your organization's quality systems - Design History File (DHF), the Device Master Record (DMR) the Device History Record (DHR), and the Technical  more...

Process Validation for Medical Devices - Webinar By GlobalCompliancePanel ...* Validation vs. Verification: Which One? * Protocol preparation * Different types of validation * IQ, OQ, and PQ Who will benefit: This webinar is targeted toward professionals involved in meeting FDA's Quality System Validation requirements: * Validation Specialists/ Managers * Process Engineers * Manufacturing Engineers * Quality Engineers *  more...

Preparing for Pre-approval Inspections - Webinar By GlobalCompliancePanel ...begins with an overview of the FDA Inspection process. Preparation for the inspection in the months before, the immediate weeks before and on the day of the inspection will be discussed. The Inspection 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  more...

Project Management for Clinical Trials - Webinar By GlobalCompliancePanel ... countries. * Decide on detailed timelines for study preparation, performance, and evaluation, including critical time points. * 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  more...

21 CFR Part 11 Complete Manual For Compliance Success - GlobalCompliancePanel Virtual Seminar - Webinar By GlobalCompliancePanel ...Host FDA Inspections o Elements and details of preparation for the inspection o Elements of the successful practices of hosting an FDA inspection when Part 11 is 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  more...

Preparing for GFSI and other Third Party Audits - Webinar By GlobalCompliancePanel ...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. Without  more...

Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine ... This Webinar is designed for people involved in document preparation and maintenance, and those who have involvement with documentation. This typically includes: * Quality Managers/ Engineers * Production/ Process Managers/ Engineers * Manufacturing Managers/ Engineers * QA and QC managers, inspectors, supervisors and personnel * Documentation Specialists *  more...

Understanding and Preparing for FDAs New Part 11 Inspection Program - Webinar By GlobalCompliancePanel ... Areas Covered In the Seminar: * FDA inspections: Preparation, conducts, follow up * Learning from past Part 11 inspections * Scope of the new Part 11 program: time frame, expected outcome * Criteria for selection of target companies * What inspectors are looking for * How to prepare your company for the upcoming inspections * Learning from previous  more...

Document Approval Control and Distribution How to Meet FDA QSR and ISO 13485 Requirements in a Cost Effective Manner - Webinar b ... often requires an inordinate amount of time spent in the preparation, submission, distribution, and implementation of change requests, document modifications, document review meetings, document approvals, and document placement. Many companies can spend MUCH LESS time and prepare MANY LESS documents, and still be in compliance with the regulations. This presentation will review the QSR and ISO  more...

Secrets of an Effective CMC Regulatory Strategy for Biopharmaceuticals Part 1 - Cell Banking - Webinar by GlobalCompliancePanel Cell banking assures that an adequate supply of equivalent well-characterized cells exist for production over the expected lifetime of the biopharmaceutical. Cell line development followed by preparation of the master/ working cell banks is an expensive process and needs to be done right the first time. Cell banks acceptable for early clinical trial material production have been found not to  more...

The FDA Tripod - Clinical Trial Regulations Compliance and GCP in Drug Development - Webinar by GlobalCompliancePanel This course provides a comprehensive review of Good Clinical Practice (GCP) and FDA regulations and requirements. Participants receive a foundation of knowledge about GCP, practical examples, and the underlying scientific and regulatory principles involved. Guidelines for each aspect of research are provided, as well as information on the structuring and preparation of protocols, consent forms,  more...

Quality Systems Inspection Technique QSIT and How to use it to Your Advantage GlobalCompliancePanel brings a new webinar on the topic of Quality Systems Inspection Technique (QSIT), and How to use it to Your Advantage Webinar will be on March 11, 2010. Webinar will be presented by Jeff Kasoff. Mr. Kasoff is the Director of Regulatory Affairs at Life-Tech, Inc., a leading manufacturer of consumables and instrumentation in the urodynamic and pain management fields. Jeff is  more...

The 510k Submission Requirements Contents and Option GlobalCompliancePanel brings a new webinar on the topic of The 510(k) Submission: Requirements, Contents, and Option. Webinar will be on March 4, 2010. Webinar will be presented by Jeff Kasoff. Mr. Kasoff is the Director of Regulatory Affairs at Life-Tech, Inc., a leading manufacturer of consumables and instrumentation in the urodynamic and pain management fields. Jeff is responsible for  more...