Anti-Corruption Compliance - Understanding the OECD Anti-Bribery Convention

August
 26 - 27 
v
Dubai - Dubai - United Arab Emirates
View Map

Course Description:

Bribery can often damage your business and your reputation. However, your business is not the only victim. The government and the society are affected more, and they are severely undermined by the weakened rule of law and damaged economic and social development. As such, governments are making anti-corruption programs an integral part of compliance. The OECD and its member countries see the core principle in fighting corruption rooted in the principle of free and fair competition. Each bribe offered or accepted compromises this principle.

This two-day training course is a practical look at corruption and current anti-corruption practices at a level that will provide both a clear definition and broad guidelines as to how this scourge can be fought. The in person seminar will discuss and detail issues and checklists to help make setting up your own anti-corruption program easier.

The seminar instructor will use a combination of prepared tuition, examples, discussions, exercises and case studies. For instance, the prominent Siemens case study that will be discussed will examine the corruption scandal and the steps that Siemens subsequently took to recover from this disaster.

This interactive course will offer participants the opportunity to share experiences and plan work within small working groups, providing practice in the application of the techniques and tools, and generating active participation.

Note: Use coupon code 232082 and get 10% off on registration.

For more details >>

Join the conversation

Upcoming events

The A to Z's of Microbial Control, Monitoring and Validation of Water Systems for Pharmaceuticals

l28 May 15 | 8:30

Course Description: All facilities manufacturing pharmaceuticals, biologics,...

Q

Elements of Current Good Manufacturing Practices

l28 May 15 | 8:30

Course Description: In this two day workshop conference you will learn the...

Q

The A to Z of Trade Compliance for a U.S. Entity

l28 May 15 | 8:30

Course Description: Trade Compliance plays a prominent role in international...

Q

Understanding the Statistical Considerations for Quantitative ICH Guidelines

l28 May 15 | 8:30

Course Description: This course is designed to introduce to individuals the...

Q

Risk Based Internal Auditing (RBIA): 2-day Comprehensive Training Workshop

l1 Jun 15 | 8:30

Course Description: Risk Based Internal Auditing (RBIA) is defined by the...

Q

Quality Control Laboratory Compliance - cGMPs and GLPs: One and a Half-day In-person Seminar

l2 Jun 15 | 8:30

Course Description: FDA inspection and oversight of quality control (QC)...

Q

Operations Risk Management and Mitigation - from Assessment to Implementation

l4 Jun 15 | 8:30

Aims Recently, a series of headline-grabbing operational risk incidents at...

Q

Human Resources and Employment Law Essentials: 2-Day In-Person Seminar

l4 Jun 15 | 8:30

Course Description: Is your company at risk for non-compliance? Is your...

Q

Managing an Effective AML Compliance Program: 2-day In-Person Seminar

l4 Jun 15 | 8:30

Course Description: Are the financial transactions within your organization...

Q

Essentials of ERM and Assessing its Effectiveness Using ISO 31000

l4 Jun 15 | 8:30

Course Description: If an internal audit is to assess the effectiveness of the...

Q

Essentials Of USP Microbiology - Reading Between the Lines of the USP General

l8 Jun 15 | 8:30

Course Description: The objective of this two day "Essentials of USP...

Q

FDA's Medical Device Software Regulation Strategy: 2-Day In-Person Seminar by Ex-FDA Official

l9 Jun 15 | 8:30

Course Description: The growth of the medical software industry outpaces the...

Q

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

l11 Jun 15 | 8:30

Course Description: Raw material requirements in a cGMP environment are often...

Q

Post-Market Compliance for Medical Devices and Evolving Reporting Requirements

l11 Jun 15 | 8:30

Course Description: This interactive one and a half day course led by Ms. Rita...

Q

Auditing the Human Resource Function & Human Resource Metrics: 2-day In-person Seminar

l11 Jun 15 | 8:30

Course Description: This seminar will cover auditing human resources practices...

Q

FDA's New Import Program Concerning International Consequences: 2-day In-person Seminar

l11 Jun 15 | 8:30

Course Description: Importing products regulated by the FDA has become more...

Q

Internal Control Best Practices for your Procure to Pay (P2P) Process

l11 Jun 15 | 8:30

Course Description: This two day seminar will focus on internal controls...

Q

Detecting and Preventing Internal and External Fraud: 2-day In-person Seminar

l18 Jun 15 | 8:30

Course Description: Organizations of all kinds and sizes are increasingly...

Q

SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations

l18 Jun 15 | 8:30

Course Description: Formal written Standard Operating Procedures (SOPs) are...

Q

Building a Vendor Qualification Program for FDA Regulated Industries

l18 Jun 15 | 8:30

Course Description: If you are looking for the answer to the following...

Q

Regulatory Compliance for Dietary Supplements in the US, EU and Canada: 2-day In-person Seminar

l25 Jun 15 | 8:30

Course Description: A growing public demand for supplements has resulted in a...

Q

Computer System Validation - Reduce Costs and Avoid 483s: 2-day In-person Seminar

l25 Jun 15 | 8:30

Course Description: Significant changes in the regulations and...

Q

21 CFR Part 11 Compliance for SaaS/Cloud Applications: 2-day In-person Seminar

l25 Jun 15 | 8:30

Course Description: Significant changes in the regulations and industry...

Q

Supplier Management for Medical Device Manufacturers

l25 Jun 15 | 8:30

Course Description: Supplier selection and management is one of the critical...

Q

Import Procedures and Documentation

l25 Jun 15 | 8:30

Course Description: This 2-day seminar is designed to assist companies that...

Q

Project Management in Human Resources: 2-Day In-Person Seminar

l25 Jun 15 | 8:30

Course Description: Naturally, getting a project to deliver on time, within...

Q

The European Clinical Trial Directive…Plus…European Filings and Registration Procedures

l25 Jun 15 | 8:30

Course Description: This interactive two day seminar will cover the various...

Q

Compliance Processes for Life Science Products in Brazil, Russia, India, China markets

l9 Jul 15 | 8:30

Course Description: This seminar will help you understand the regulatory,...

Q

Technical and Regulatory Writing for FDA Regulated Industries

l9 Jul 15 | 8:30

Course Description: Regulatory professionals have to write highly technical...

Q

OCEG approved GRC (Governance, Risk and Compliance) Professional Seminar

l15 Jul 15 | 8:30

Course Description: This GRC Professional Seminar will teach you how to...

Q

Why is FDA at my facility, and what do I do during an inspection?: 2-day In-person Seminar

l8 Oct 15 | 8:30

Course Description: This two day course will prepare firms for a quick,...

Q

Regulatory Crisis Management: Best Practices for Dealing with the Common Crisis Events

l12 Nov 15 | 8:30

Course Description: Unlike risk management, which involves managing potential...

Q