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Certified Fraud Examiner (CFE)

Certified Fraud Examiner (CFE)

Location: , Belgium
Category: Education
Start Date: 03-19-2018 Last Day: 03-23-2018
Master the skills and knowledge you need to pass the CFE exam by attending this ACFE accredited 5-day Certified Fraud Examiner (CFE) course Strengthen your anti-fraud skills and become a Certified Fraud Examiner (CFE) now! Master the skills and knowledge you need to pass the CFE exam by attending this official Certified Fraud Examiner (CFE) course and become a CFE now! This 5-day, instructor-led course will help you master the concepts tested at the CFE exam: Financial Transactions and Fraud Schemes Legal aspects related to Fraud Investigation Fraud Fraud Prevention and Deterrence About the ACFE (Association of Certified Fraud Examiners)…
60th London International Youth Science Forum

60th London International Youth Science Forum

Location: , United Kingdom
Category: Education
Start Date: 07-25-2018 Last Day: 08-08-2018 Deadline for abstracts: 07-24-2018
60th LONDON INTERNATIONAL YOUTH SCIENCE FORUM (LIYSF) The annual London International Youth Science Forum (LIYSF) is a two-week residential course hosted at the renowned research university Imperial College London. Our aim is to unite outstanding talent from all nations and provide a deeper insight into science and its applications for the benefit of all mankind. The forum attracts 500 of the globe’s leading young scientists, aged from 16-21 and visiting from over 65 countries. Along with an active social calendar and a focus on cultural education and forming lasting friendships, the program includes lectures, demonstrations from leading scientists and visits…
Feira internacional de pos-graduacao: QS World Grad School Tour Lisboa

Feira internacional de pos-graduacao: QS World Grad School Tour Lisboa

Location: , Portugal
Category: Education
Start Date: 03-20-2018 Last Day: 03-20-2018 Deadline for abstracts: 03-19-2018
Encontre a pos-graduacao perfeita para voce na QS World Grad School Tour em Lisboa! Registre-se gratis: http://bit.ly/2zJiEnb Por que participar: Fale diretamente com diretores de admissao das melhores universidades Assista seminarios gratuitos Receba dicas sobre os testes preparatorios Concorra a bolsas de estudo exclusivas e muito mais! Price: QS World Grad School Tour - Lisboa: EUR 0.00. Time: 2:30 pm to 8:00 pm.
Emergency Preparedness – What To Do In Case of Fire, Flood, Tornado, Bomb Threat, Power Outage, etc

Emergency Preparedness – What To Do In Case of Fire, Flood, Tornado, Bomb Threat, Power Outage, etc

Location: , United States
Category: Education
Start Date: 01-10-2018 Last Day: 01-10-2018 Deadline for abstracts: 01-10-2018
OVERVIEW Having an effective Emergency Response Plan can make the difference between life and death in an emergency. What would you do in case of a fire, flood, tornado, etc.? Do you and your Employees know what to do? Do you have written Emergency Response Plans in place? Have you conducted an annual Fire Drill? What would you do if an Active Shooter Scenario happened at your location? WHY SHOULD YOU ATTEND OSHA requires that Employees be trained in Emergency Response Preparedness. Companies are required to have written Emergency Response Plans that address the questions outlined above. This webinar will…
Dessekilet International Leadership Conference

Dessekilet International Leadership Conference

Location: , Canada
Category: Education
Start Date: 01-11-2018 Last Day: 01-15-2018 Deadline for abstracts: 11-14-2017
Meet 500+ multi-disciplinary doctors, lawyers, teachers, social workers, mental health professionals, and many others. Don't miss this prime opportunity to exhibit your: business tools and services for nonprofits.
Product Reliability Training Courses | Product Reliability Testing

Product Reliability Training Courses | Product Reliability Testing

Location: , United States
Category: Education
Start Date: 01-29-2018 Last Day: 01-30-2018 Deadline for abstracts: 01-28-2018
Course "Predicting & Improving Product Reliability" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Although a primary objective of reliability analysis is to improve product reliability, there are many possible reasons for collecting and analyzing reliability data. Several examples are the following: • Assessing product reliability in the field • Predicting product warranty costs • Estimate replacement part/spares requirements • Assessing the effect of a proposed design change • Demonstrating product reliability to customers or government agencies • Comparing components from multiple suppliers • Comparing components from…
Internal Audit Checklist for Medical Devices | Quality Audit

Internal Audit Checklist for Medical Devices | Quality Audit

Location: , United States
Category: Education
Start Date: 01-25-2018 Last Day: 01-26-2018 Deadline for abstracts: 01-23-2018
Course "Quality Audits for the Medical Device Industry" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Quality audits are an important element in implementing and maintaining an effective Quality Management System (QMS). Audits are one of the most powerful tools that management has to assure on effective QMS. In this workshop, participants examine the various types of audits to understand their role. Internal quality audits (1st party) help a company evaluate itself. Customer/supplier audits (2ndparty) play a role in an effective supplier management program; your company could…
What is Process Validation Report | 21CFR11 Compliance Checklist 2018

What is Process Validation Report | 21CFR11 Compliance Checklist 2018

Location: , Germany
Category: Education
Start Date: 01-11-2018 Last Day: 01-12-2018 Deadline for abstracts: 01-09-2018
Course "Validation and 21 CFR Part 11 Compliance of Computer Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Computer Systems Validation (CSV) also known as Software Validation is all-pervasive in the Life Sciences Industry. It is a requirement of all the predicate rules, as well as 21 CFR 11 and Annex 11. However, unless one knows how to implement CSV, it is often very hard to detect the requirement for CSV, and very hard to determine what needs to be done, to meet domestic and /…
Pharmaceutical Validation Guidelines | 21 CFR Part 11 Compliance 2018

Pharmaceutical Validation Guidelines | 21 CFR Part 11 Compliance 2018

Location: , Switzerland
Category: Education
Start Date: 01-08-2018 Last Day: 01-09-2018 Deadline for abstracts: 01-07-2018
Course "Validation and 21 CFR Part 11 Compliance of Computer Systems" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: Computer Systems Validation (CSV) also known as Software Validation is all-pervasive in the Life Sciences Industry. It is a requirement of all the predicate rules, as well as 21 CFR 11 and Annex 11. However, unless one knows how to implement CSV, it is often very hard to detect the requirement for CSV, and very hard to determine what needs to be done, to meet domestic and /…
Feira internacional de MBA: QS World MBA Tour Sao Paulo

Feira internacional de MBA: QS World MBA Tour Sao Paulo

Location: , Brazil
Category: Education
Start Date: 02-06-2018 Last Day: 02-06-2018 Deadline for abstracts: 02-06-2018
Encontre o MBA perfeito para voce na QS World MBA Tour em Sao Paulo! Registre-se gratis: http://bit.ly/2hARNFA Por que participar: . Fale diretamente com diretores de admissao dos melhores MBAs internacionais . Assista seminarios gratuitos . Receba dicas sobre os testes preparatorios, como o GMAT . Concorra a bolsas de estudo exclusivas e muito mais! Price: QS World MBA Tour - Sao Paulo: BRL 0.00 Time: 4:30 pm to 9:00 pm
QS Connect MBA - Lisboa

QS Connect MBA - Lisboa

Location: , United Kingdom
Category: Education
Start Date: 03-12-2018 Last Day: 03-12-2018 Deadline for abstracts: 03-11-2018
Se voce esta pronto(a) para dar o proximo passo na sua carreira, mas ainda nao tem certeza sobre qual programa de MBA escolher, nao perca a oportunidade de participar do QS Connect MBA e se encontrar pessoalmente com algumas das escolas de negocios mais renomadas internacionamente. Reserve sua vaga gratuitamente: http://bit.ly/2AKgZgq 4 passos para agendar suas entrevistas: 1. Faca sua inscricao 2. Anexe seu curriculo em Ingles ao seu perfil ou envie para resume@qs.com 3. Nossos consultores e as escolas irao analisar seu perfil e enviarao seus convites para as entrevistas 4. Confirme sua presenca Price: QS Connect MBA -…
QS Connect MBA - São Paulo

QS Connect MBA - São Paulo

Location: , Brazil
Category: Education
Start Date: 02-05-2018 Last Day: 02-05-2018 Deadline for abstracts: 02-04-2018
Se você está pronto(a) para dar o próximo passo na sua carreira, mas ainda não tem certeza sobre qual programa de MBA escolher, não perca a oportunidade de participar do QS Connect MBA e se encontrar pessoalmente com algumas das escolas de negócios mais renomadas internacionamente. Reserve sua vaga gratuitamente: http://bit.ly/2z3N0Ux 4 passos para agendar suas entrevistas: 1. Faça sua inscrição 2. Anexe seu currículo em Inglês ao seu perfil ou envie para resume@qs.com 3. Nossos consultores e as escolas irão analisar seu perfil e enviarão seus convites para as entrevistas 4. Confirme sua presença Price: QS Connect MBA -…
QS Connect MBA - Rio de Janeiro

QS Connect MBA - Rio de Janeiro

Location: , Brazil
Category: Education
Start Date: 02-03-2018 Last Day: 02-03-2018 Deadline for abstracts: 02-02-2018
Se voce esta pronto(a) para dar o proximo passo na sua carreira, mas ainda nao tem certeza sobre qual programa de MBA escolher, nao perca a oportunidade de participar do QS Connect MBA e se encontrar pessoalmente com algumas das escolas de negocios mais renomadas internacionamente. Reserve sua vaga gratuitamente: http://bit.ly/2mxBxXB 4 passos para agendar suas entrevistas: 1. Faca sua inscricao 2. Anexe seu curriculo em Ingles ao seu perfil ou envie para resume@qs.com 3. Nossos consultores e as escolas irao analisar seu perfil e enviarao seus convites para as entrevistas 4. Confirme sua presenca
Feira internacional de pos: QS World Grad School Tour Rio de Janeiro

Feira internacional de pos: QS World Grad School Tour Rio de Janeiro

Location: , Brazil
Category: Education
Start Date: 02-03-2018 Last Day: 02-03-2018 Deadline for abstracts: 02-02-2018
Encontre a pos-graduacao perfeita para voce na QS World Grad School Tour no Rio de Janeiro! Registre-se gratis: http://bit.ly/2zGIw5m Por que participar: Fale diretamente com diretores de admissao das melhores universidades Assista seminarios gratuitos Receba dicas sobre os testes preparatorios Concorra a bolsas de estudo exclusivas e muito mais! Price: QS World Grad School Tour - Rio de Janeiro: BRL 0.00. Time: 12:30 pm to 6:00 pm.
Feira internacional de pós-graduação: QS World Grad School Tour São Paulo

Feira internacional de pós-graduação: QS World Grad School Tour São Paulo

Location: , Brazil
Category: Education
Start Date: 02-01-2018 Last Day: 02-01-2018 Deadline for abstracts: 01-31-2018
Encontre a pós-graduação perfeita para você na QS World Grad School Tour em São Paulo! Registre-se grátis: http://bit.ly/2iiTe8B Por que participar: • Fale diretamente com diretores de admissão das melhores universidades • Assista seminários gratuitos • Receba dicas sobre os testes preparatórios • Concorra a bolsas de estudo exclusivas e muito mais! Price: QS World Grad School Tour - São Paulo: BRL 0.00 Time: 2:30 pm to 8:00 pm
Aware of the Similarities and Differences in the files

Aware of the Similarities and Differences in the files

Location: , United States
Category: Education
Start Date: 01-31-2018
Overview: It will also consider the European Union's MDD TF/DD requirements, and evaluate the documents' differing purposes / goals, as well as the two different device classification schemes. Why should you Attend: companies go global, they must meet different product design documentation. The cGMPs mandate Design Control and the Design History File (DHF). In order to sell globally, the EU's CE-marking documentation is a requirement - the Technical File or Design Dossier. Areas Covered in the Session: DHF "Typical" Contents and Deliverables The DMR and DHR / Lot / Batch Record TF / DD Required Contents Parallel Approaches to Documentation…
Which data and systems are subject to Part 11

Which data and systems are subject to Part 11

Location: , United States
Category: Education
Start Date: 01-16-2018
Overview: This webinar details the regulation and how it applies to computerized systems. Learn exactly what is needed to be compliant for all three primary areas: SOPs for the IT infrastructure, industry standards for software product features, and the 10-step risk-based validation approach. Areas Covered in the Session: Which data and systems are subject to Part 11 What Part 11 means to you, not just what it says in the regulation Avoid 483 and Warning Letters Explore the three primary areas of Part 11 compliance: SOPs, software product features, and validation documentation Ensure data integrity, security, and protect intellectual property…
The Value of a Human Factors Program

The Value of a Human Factors Program

Location: , United States
Category: Education
Start Date: 01-12-2018
Overview: This webinar will explain the implementation of ISO 62366 and the regulatory expectations discussed in the 2016 FDA Guidance for a compliant human factors/ usability program. Why should you Attend: This year FDA published their priority list for the completion of their Guidance documentation. This annual activity gives us inspection and enforcement insight into the priorities within the agency. Interoperability and Cybersecurity were in the top 3. The implementation of a robust HF program will include both of these disciplines. Following the implementation of the results of a Human Factors/ Usability study, a validation of the safety and effectiveness…
Ensuring Data Integrity and Safety in Clinical Research

Ensuring Data Integrity and Safety in Clinical Research

Location: , United States
Category: Education
Start Date: 01-09-2018
Overview: Electronic medical records and electronic handling of study data is increasingly common. To involve computer systems in clinical research implies knowledge of 21 CFR Part 11. Why should you Attend: The increasing use of computers and increasing complexity, all persons who have any data input requirements to know the set-up and function of the systems they are using. Forewarned is forearmed. Areas Covered in the Session: The CFR definitions of Electronic Record, Electronic Signature, Closed System, Open System, Data Trails, and assure that your data is secure and valid? What needs to happen to make data trails secure and…
Act for Transportation and Logistics Professionals

Act for Transportation and Logistics Professionals

Location: , United States
Category: Education
Start Date: 01-08-2018
Overview: The FSMA is paradigm shift that moves the focus from food inspections to preventative measures and process compliance. Why should you Attend: Specific provisions of the FSMA that impacts transportation and 3rd party logistics providers Sanitary transportation best practices To develop a food safety plan that identifies potential risks, preventative controls and ongoing monitoring New rules that govern food importers and exporters Areas Covered in the Session: How the trend toward transparency and widespread supply chain knowledge (among consumers) will impact sourcing decisions Why sustainable supply chains will become more mainstream, especially among luxury buyers and millennials Why low…

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