Congrès management - Formation management

How to Think Like a Crook - Money Laundering Prevention

Réf: 30807 Mercredi 11 Décembre 2019 - Palo Alto ^US

Editorial This anti-money laundering training will describe the reasons and methods of money laundering in financial institutions. This will help attendees to protect themselves from regulatory risk by establishing an effective anti-money laundering system within their financial ...

FDA Inspections: Understanding the Core Elements – Part I

Réf: 30733 Jeudi 12 Décembre 2019 - Palo Alto ^US

Editorial Attend this course to learn the rationale, strategies and flow on how to plan for an FDA inspection, the inspection process and approach, and which company roles should be assigned for these types of inspections, among other related topics. Objectives This course is designed to ...

A New Role for Project Controls Professionals on Dispute Boards

Réf: 30820 Jeudi 12 Décembre 2019 - Palo Alto ^US

Editorial Attend this webinar to learn how project controls professionals can add value to the DRB process and help contribute to dispute resolution on many projects as members of Dispute Resolution Boards. Objectives Learn about the DRB process. Understand the benefits and concern ...

NLRB Effects on Social Media, Non-Union Employers and Other Changes

Réf: 30890 Jeudi 12 Décembre 2019 - Palo Alto ^US

Editorial This NLRA compliance webinar will discuss the fundamentals of NLRA and review how recent decisions of the National Labor Relations Board (NLRB) affects both non-union and union employers.
  Objectives What is the National Labor Relations Act and how does it apply to ...

FDA Inspections: Understanding the Core Elements – Part I

Réf: 31050 Jeudi 12 Décembre 2019 - Palo Alto ^US

Editorial Attend this course to learn the rationale, strategies and flow on how to plan for an FDA inspection, the inspection process and approach, and which company roles should be assigned for these types of inspections, among other related topics.
  Objectives This course is ...

FDA Inspections: Understanding the Core Elements – Part I

Réf: 31058 Jeudi 12 Décembre 2019 - Palo Alto ^US

Editorial Attend this course to learn the rationale, strategies and flow on how to plan for an FDA inspection, the inspection process and approach, and which company roles should be assigned for these types of inspections, among other related topics.
  Objectives This course is ...

Operational Risk Scenario Analysis

Réf: 31081 Jeudi 12 Décembre 2019 - Palo Alto ^US

Editorial Scenario analysis complements the risk assessment process, which often overlooks material events that only happen infrequently, such as natural disasters, acts of terrorism, and data breaches. This webinar will highlight the importance of scenario analysis, its objectives and expected ...

Good Documentation Practice (GDocP) for FDA Regulated Industry

Réf: 30734 Lundi 16 Décembre 2019 - Palo Alto ^US

Editorial This good documentation practice webinar will discuss how to secure, manage and govern your documentation in compliance with GxP/GMP requirements and be able to pass quality audit. Also attendees will learn the connection between CxP/GMP and document control, which documents need to ...

Good Documentation Practice (GDocP) for FDA Regulated Industry

Réf: 30742 Lundi 16 Décembre 2019 - Palo Alto ^US

Editorial This good documentation practice webinar will discuss how to secure, manage and govern your documentation in compliance with GxP/GMP requirements and be able to pass quality audit. Also attendees will learn the connection between CxP/GMP and document control, which documents need to ...

Good Documentation Practice (GDocP) for FDA Regulated Industry

Réf: 31060 Lundi 16 Décembre 2019 - Palo Alto ^US

Editorial This good documentation practice webinar will discuss how to secure, manage and govern your documentation in compliance with GxP/GMP requirements and be able to pass quality audit. Also attendees will learn the connection between CxP/GMP and document control, which documents need to ...

Handling OOS Test Results and Completing Robust Investigations

Réf: 30743 Mardi 17 Décembre 2019 - Palo Alto ^US

Editorial This webinar will review the regulatory requirements for investigating an OOS Investigation. The responsibilities of the analyst, the supervisor and QA will be discussed. A detailed flow chart will be used to help the attendees clearly understand the steps and the order in which they ...

What To Expect From FDA’s New Approach to Regulate Medical Software

Réf: 30744 Mardi 17 Décembre 2019 - Palo Alto ^US

Editorial The FDA’s emerging approach to medical software product regulation has important ramifications for patients, healthcare providers and insurers as well as product developers. So, it is critically important for companies throughout the life sciences and healthcare industries that ...

FDA: Mock and Pre-Approval Inspections (PAIs) - Part II

Réf: 30745 Mardi 17 Décembre 2019 - Palo Alto ^US

Editorial This course for pharmaceutical professionals provides the information they require, to prepare for and understand what will happen during a mock audit and during a Pre-Approval Inspection (PAI).
  Objectives This course will provide you with the purposes of FDA’s ...

How to Conduct an Internal Harassment and Bullying Investigation to Determine Facts and Minimize Liability

Réf: 30895 Mardi 17 Décembre 2019 - Palo Alto ^US

Editorial This webinar undertakes to explain the process of internal harassment and bullying investigation. Participants will learn how to handle harassment complaints and conduct the investigation to determine facts and minimize liability by analysing evidences, drawing conclusions, writing ...

Handling OOS Test Results and Completing Robust Investigations

Réf: 31061 Mardi 17 Décembre 2019 - Palo Alto ^US

Editorial This webinar will review the regulatory requirements for investigating an OOS Investigation. The responsibilities of the analyst, the supervisor and QA will be discussed. A detailed flow chart will be used to help the attendees clearly understand the steps and the order in which they ...

What To Expect From FDA’s New Approach to Regulate Medical Software

Réf: 31063 Mardi 17 Décembre 2019 - Palo Alto ^US

Editorial The FDA’s emerging approach to medical software product regulation has important ramifications for patients, healthcare providers and insurers as well as product developers. So, it is critically important for companies throughout the life sciences and healthcare industries that ...

FDA: Mock and Pre-Approval Inspections (PAIs) - Part II

Réf: 31065 Mardi 17 Décembre 2019 - Palo Alto ^US

Editorial This course for pharmaceutical professionals provides the information they require, to prepare for and understand what will happen during a mock audit and during a Pre-Approval Inspection (PAI).
  Objectives This course will provide you with the purposes of FDA’s ...

Enhancing Audit Advisory Practices

Réf: 30808 Mercredi 18 Décembre 2019 - Palo Alto ^US

Editorial Today’s Internal Audit groups are expected to do more than just assurance work. They are required to provide management with industry best practices, trends in risk management and perform advisory reviews of emerging and topical areas. This webinar introduces a new tool that helps ...

I-9 Audits: Strengthening Your Immigration Compliance Strategies

Réf: 30974 Mercredi 18 Décembre 2019 - Palo Alto ^US

Editorial This webinar will help employers understand how to comply with the Form I-9 process, avoid fines for non-compliance, and understand key requirements to aid in efforts to maintain compliance. Objectives Mastering Form I-9 completion, storage, and retention ...

Stability Studies and Estimating Shelf Life

Réf: 31066 Mercredi 18 Décembre 2019 - Palo Alto ^US

Editorial In this webinar attendees will learn the useful methods and techniques for conducting a stability study and analyzing the resulting data for estimating shelf life. This webinar will provide the answers to help participants immediately apply the presented methods. The interpretation ...

Drug Manufacturing Inspection Part III

Réf: 30746 Jeudi 19 Décembre 2019 - Palo Alto ^US

Editorial Attend this course to prepare for and understand what will happen during a Drug Manufacturing Inspection for Surveillance Inspections. It will explain the FDA criteria to perform a For Cause Inspection. Objectives This course will provide you with the system wide controls the FDA ...

Marketing the Banker in Today's Competitive Environment - 4Ps of Marketing, Industry Life Cycle & Market Structure

Réf: 30963 Vendredi 20 Décembre 2019 - Palo Alto ^US

Editorial This practical training program will help understand how to better market the bank, a bank department, and yourself in this very competitive world. The webinar will review the marketing concept and its practical application in marketing bank products and services. The webinar will ...

How To Establish an Effective Chief Compliance Officer's (CCO) or Chief Risk Officer's (CRO) Function - Organization and Responsibilities

Réf: 30944 Jeudi 23 Janvier 2020 - Palo Alto ^US

Editorial This training will provide valuable knowledge on what companies need to do to establish an "effective" Compliance Office that leads to conceiving, developing and implementing successful GRC programs and provides top level coordinating leadership for governance, risk management and ...

41st World Dental Science and Oral Health Congress

Réf: 30440 25/03/2020 -> 26/03/2020 - En ligne

Dental Science Congress 2019

Big Data Hadoop Training | Hadoop Certification Online - Simpliv

Réf: 26892 28/03/2018 -> 30/12/2019 - 94539 ^US

Big Data Hadoop Training | Hadoop Certification Online - Simpliv