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Applicable Training Seminars and Classes

From QLogy Management Services Pvt. Ltd

ITIL Expert for only Rs one lac through knowledgecredits offered by QLogy ...sing Warranty in Bangalore. Note: - This offer cost is applicable if and only if you purchase the trainings from www. knowledgecredits. com We strongly recommend you to create free account on our e-Learning (Learning Management) portal i. e. and go through the ITIL Sample papers, recorded webinars for Information Technology Infrastructure Library( ITIL), Integrated Quality Management(I more...

Knowledge Credits inaugural offer on ITIL Trainings offered by Qlogy ...% Passing Warranty in Pune. Note: - This offer cost is applicable if and only if you purchase the trainings from www. knowledgecredits. com We strongly recommend you to create free account on our e-Learning (Learning Management) portal i. e. and go through the ITIL Sample papers, recorded webinars for Information Technology Infrastructure Library( ITIL), Integrated Quality Management(I QM), more...

From HR Learning Center LLC

Top Tips For Managers to Prevent Harassment in your Workplace

...ny's Sexual and Unlawful Harassment Policy, including the applicable managers to whom sexual and unlawful harassment complaints should be reported. HR Learning Centera ™s Anti-Harassment Training Seminar provides an in-depth look at sexual and unlawful harassment including a definition of sexual harassment, discussions of quid pro quo and hostile work environment harassment. The Seminar more...

From Webucator

Introduction to SQL Training

This SQL training course is designed for students new to writing SQL queries. A typical student will need to learn SQL to build applications or to generate business reports. For the most part, the SQL learned in the course is applicable to all major databases. In the few cases in which there are differences between the databases, these differences will be pointed out. more...

Intermediate Java Training

...sion of the Java language and Core API; but it is equally applicable to Java 5 and groups looking for Java training who know they ' ll be using Java 5 are encouraged to use this course. For training within the Java 1.4 environment, please see version 1.4.3 of this course, which works to the old version but looks ahead to some Java-5/6 language features; to read more about different versions of more...

From GlobalCompliancePanel

GxP Computer System Validation The investigators Point of View - Webinar By GlobalCompliancePanel Overview: The webinar explains what is needed to prepare for an audit or regulatory inspection. It addresses SOPs for the GxP and IT infrastructure, hardware and software qualification, computer system validation, and change control for revalidation. This event is applicable to regulated companies and software vendors. Tuesday, July 10, 2012 10: 00 AM PDT | 01: 00 PM EDT more...

RAPS Approved Seminar on Risk Management in Medical Devices Industry at Mumbai ...velopment. International consensus, reflected in globally applicable standard requirements, has led to risk management as a mandatory component of almost any activity in the medical device industry. The course will emphasise the implementation of risk management into the development and maintenance process. It will use real-life examples and proven tips and tricks to make the application of more...

Risk Management in IEC 60601-1 Third Edition - Webinar By GlobalCompliancePanel ...riptive in many areas The new standard requires that all applicable collateral and particular standards must be used for compliance Current activities leading to full implementation of the standard Available documents to guide implementation of the Third Edition Who Will Benefit: Design Engineers Quality Engineers and Managers Compliance Engineers Engineering Managers Project Managers more...

A Simpler Approach to Implementing or Validating CGMPs to 21 CFR 11 Electronic Records Signatures - Webinar By GlobalComplianceP ..."Electronic Records" / "Electronic Signatures", and other applicable industry software validation models, coupled with the ISO 14971 / ICH Q9 Product Risk Management models, to structure, run, and document acceptable cGMP Part 11 software validations. The FDA and other regulatory agencies have stated that software validation can realistically only be accomplished effectively if "risk-based". more...

Design Planning and Conducting Effective Audits - Webinars by gcp Internal quality system audits should be viewed as an improvement tool. Too often due they have a negative connotation and are viewed as a necessary evil. Effective audits can comply with the regulations and also be a source of improvement. more...

Design Planning and Conducting Effective Audits by gcp Internal quality system audits should be viewed as an improvement tool. Too often due they have a negative connotation and are viewed as a necessary evil. Effective audits can comply with the regulations and also be a source of improvement. more...

Auditing and Administrating Human Resources Policies and Practices by TrainHR ...rent human resources policies that are in compliance with applicable laws and convey the desired practices in your organization. Policy should be reviewed and updated periodically and through this webinar you can review your current policies, clarify policies for easier administration, and perhaps add new policies others to address new situations and circumstances in your workplace. Well more...

Auditing an Active Pharmaceutical Ingredient API Contract Manufacturing Organization CMO - Webinar By GlobalCompliancePanel ...ocus on during any on-site audit. While understanding the applicable GMP is important, how to apply the GMP and what to establish with a CMO is critical to your supply chain. Areas Covered in the Session: * Examine key elements of an API audit * Audit preparation * The audit itself o Opening Session o Audit itself o What to look for? more...

Develop and Execute the Company Software VV Program - Webinar By GlobalCompliancePanel ..."Electronic Records" / "Electronic Signatures", and other applicable industry software validation models, coupled with the ISO 14971 / ICH Q9 Product Risk Management models, to structure, run, and document acceptable software validations. The FDA and other regulatory agencies have stated that software validation can realistically only be accomplished effectively if "risk-based". How can this be more...

The Most Common Problems in FDA Software Validation Verification- Webinar By GlobalCompliancePanel ... staff the practical information needed to understand the applicable regulations and solid methods to document compliance. * FDA inspectors are now being trained to evaluate software validation practices. * Increasing use of automated manufacturing and quality systems means increased exposure. * Most recalls can be traced back to computerized equipment, exposing the validation more...

Requirements of the Master Production Record - Webinar By GlobalCompliancePanel ...ompliance requirements for the master production records. Applicable areas may include clinical, technology transfer, and routine manufacturing and packaging for the API and finished commercial product. It is the intent of this program to enable your firm to have a consistent, compliant approach and maintain continuous improvement in the area of production records. With the information gained more...

Best Practices for the Implementation and Use of Test Management Tools - Webinar By GlobalCompliancePanel ...mplementation of any regulated application, therefore all applicable SDLC documents, vendor audits, validation/ qualifications, operation/ support, training and general use of the Test Management Tool must be considered, prior to deciding if a Test Management Tool should be used to maintain the companies corporate validation policies. This presentation will provide details regarding more...

Bringing Compliance To Design Control For Older Products - Webinar By GlobalCompliancePanel Overview: The webinar examines critical parts of design control after product release including: design change control, design validation, and the Design History File. The webinar is designed to help regulatory Affairs, Quality Engineers, and Design Engineers maintain released products within current regulatory requirements. As an attendee you will learn what the FDAs expectations for your more...

Purchasing and Supplier Controls in the Medical Device Industry - Webinar By GlobalCompliancePanel ...ace to routinely assess your suppliers, and set forth the applicable criteria they must meet to remain "approved." You never have to pay a visit to your supplier if you have a great supplier control program in place. Areas Covered In the Seminar: * How to qualify new suppliers in a cost efficient manner * How to assess current suppliers in a cost efficient manner * How to more...

FDAs Proposed Rule Regarding Device Establishment Registration and Listing and How to Register and List - Webinar By GlobalCompl ...ed changes to Implement the provision of Bioterrorism Act applicable to imported devices * Other proposed Amendments that would change current device establishment registration and listing requirements * Replacement of the current regulations regarding updating device listing information outside the required update periods * Clarification of who must provide establishmentsa more...

Project Management in a cGMP Environment - Webinar By GlobalCompliancePanel ... design and/ or change control, with consideration of all applicable standards. The EU MDD and their notified bodies are no different. How can this be done from a project's inception? How can a Project Leader or Project Manager ensure critical elements are not omitted until late in the project when disaster looms? How to minimize scope creep? How to conclude a project "on time" and "within more...

Legal Risks in Social Media for Healthcare Providers - Webinar By GlobalCompliancePanel ...nvironment, but most are concerned that the special rules applicable to the healthcare industry prevent or restrict their activities. In fact, the healthcare industry is subject to particularly restrictive rules that impact the manner and method with which they can use social media tools, particularly related to HIPAA and other medical privacy concerns. However, it is possible to pursue a more...

Webinar on Pharmacovigilance Audit - Webinar by GlobalCompliancePanel ...ty 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, assessment and reporting of adverse event cases, the more...

Good Documentation Practices in a Regulated Environment - Webinar by GlobalCompliancePanel Whether you work in production or in a laboratory or if you conduct investigations or finalize product release, sound data and information is essential to success and compliance. To ensure success, and avoid those frustrating, embarrassing discussions of missing or doubtful data, employees recognize and must follow Good Documentation Practices (GDP). These practices apply to all pharmaceutical 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...

Combination Products FDAs Proposed Rule for GMP Requirements and Introduction and Expectations for Combo Products - Webinar by G ...e current good manufacturing practice (cGMP) requirements applicable to combination products. This proposed rule is intended to promote the public health by clarifying which cGMP requirements apply when drugs, devices, and biological products are combined to create a combination product. In addition, the proposed rule sets forth a transparent and streamlined regulatory framework for firms to more...

Importing and Exporting Medical Devices A Primer on Regulatory Strategy and Requirements Any medical device that is legally in the U. S. may be exported anywhere in the world without prior FDA notification or approval. The export provisions under section 802 of the FD&C Act only applies to unapproved devices. Devices that have not been approved or cleared in the U. S. must follow the export provisions of the FD&C Act. Foreign firms that manufacture medical devices and/ or products more...

From Marsden International (UK) Ltd

ISO 14001 Online Auditor Course ISO 14001 online training course provides 6 modules each containing around 50 slides. Each module covers aspects of the audit process as well as detailed information on ISO 14001 itself. The course contains multi-media speech, photos and extensive video which enables delegates to fully understand the audit process. The course is IEMA-approved which means that you obtain a certificate after more...

From Business901

Marketing Your Black Belt Marketing Your Black Belt How Good are you at Marketing Yourself? Presentation on "How to Market Black Belt Services!" All Attendees will receive a Free download of How to Achieve Expert Status in 2010 Cana ™t make this time, please contact us for other available times. I believe that Lean Six Sigma Consulting has the greatest opportunity ever and in my terms, more...

From Bid-Winners

Introduction to the Tendering Process An introductory course that explains how the bidding process works in Canada. This course is prerequisite for more advanced courses. 1- Government Tenders vs. Private Sector RFPs 2- Where to find RFPs and Tenders 3- Primer on how to understand Tender documents 4- Primer on how to write proposals for Tenders Attendees Receive: a 15 days of free email support for after-class Q&A more...

From Global BioPharmaceutical Resources, Inc. (GBPR, Inc.)

How to be Compliant and competitive ...applicable regulations is imperative and it is usually well understood how this can be achieved. However, in a highly competitive and increasingly global marketplace, mere compliance is insufficient for success. Competitiveness must be achieved not only through cost efficient manufacture and supply, but also by achieving compliance at the right cost level. Whereas compliance is mainly seen as a more...

From Pioneer Engineering

Time Waveform Analysis Vibration

...us a practical portion. Exam is closed book. A sheet of applicable equations is provided. Maximum # Students: None Recommended Text: Time Domain Analysis, Stansloski Course Objectives Students who successfully complete this course will be able to: a Set up proper collection specifications for time domain analysis a Understand the differences from the frequency more...

From Business Expert Webinars

Project Management Leadership ...on-task, and supported by the team and his methodology is applicable for projects in any department in the workplace. As the project manager, you will feel empowered by Gary as he mentors you through the development of a process that leads you to project victory. In this webinar, you'll learn how to: Prepare a project charter to ensure the project is scoped correctly Effectively more...