Instructor Led Compliance Training in Delaware, USA
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Compliance Seminar Schedule
| Program | Location | |||
|---|---|---|---|---|
May, 2012 | ||||
| 2nd May | IRS Form 1099 Reporting: What You Need to Know | Wilmington, DE | [Register] | |
From Compliance LLC
Certified Solvency ii Professional (CSiiP)
...the knowledge and skills needed to understand and support compliance with the Solvency ii Directive of the European Union.
Target Audience:
This course is intended for decision makers, managers, professionals and consultants that:
A. Work in Insurance or Reinsurance firms of EEA countries.
B. Work in Groups - Financial Conglomerates (FC), Financial Holding Companies (FHC),
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Certified Solvency ii Equivalence Professional (CSiiEP) - Preparing for Equivalence with the Solvency ii Directive of the EU
Objectives:
This course has been designed to provide with the knowledge and skills needed to understand the Solvency ii and the Reinsurance directives of the EU, and their extraterritorial application to non-EU countries.
The course provides with the skills needed to pass the Certified Solvency ii Equivalence Professional (CSiiEP) exam.
Target Audience:
This course is intended for
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From GlobalCompliancePanel
Statistics for the Non-Statistician - US Seminar 2012 at Washington DC
...se will help you to use statistics correctly and minimize compliance risk.
Statistical tools and techniques are very commonly used to help measure and improve the quality of a firm's process and product. If statistical analysis is not properly performed and/ or understood, a firm can run the risk of distributing product to the market that ultimately fails eventually resulting in lost time
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HIPAA Privacy Security and Breach Notification Compliance Understanding the Requirements Preventing Incidents Surviving Audits a
... designed to provide intensive, two-day training in HIPAA compliance, including what's currently in the regulations, whata s changing, and whata s going to need to be addressed by covered entities and business associates in the near future. The session provides the background and details for any manager of healthcare information privacy and security to know what are the most
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DHF DMR DHR and TF - Regulatory Documents Explained and Best Practices for Controlling Them - US Seminar 2012 at Pennsylvania
...compliance with FDA and ISO regulations, there are many documents that must be maintained by your firm.
From the earliest phases of the design process all the way through manufacturing and distribution, all aspects of your plans and records must be documented. As well known as these requirements are, thata s the extent to which they are fraught with potential deficiencies. Similarly
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USFDA EU Essentials of Drug Safety and Pharmacovigilance - India Seminar 2012 at Mumbai
This training course is designed to give pharmaceutical and
biologic companies operating in the U. S. and EU an
understanding of product safety and regulatory compliance.
The course will include case studies of adverse events to
illustrate the decision-making process and reasoning
needed behind when and how to properly report incidents to
regulatory authorities.
Date and Venue
March 5th,
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