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Third International Conference on Electrical Engineering and Information Technologies for Rail Transportation (EITRT 2017)
Oct. 20-22, 2017, Changsha, China

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Conference	Deadline	Date	Country
1.Webinar on HIPAA for HR - Some Good News for Employers	2017-09-28	2017-09-28	U.S.A
2.Structuring Physician Practice Acquisitions: Key Stark Law Considerations webinar by MentorHealth	2017-09-28	2017-09-28	U.S.A
3.Webinar on 2017 HIPAA Audits - an Insider's Perspective	2017-09-19	2017-09-19	U.S.A
4.Structuring and Auditing Medical Director Arrangements: Key Stark Law Considerations	2017-09-07	2017-09-07	U.S.A
5.2017 Webinar on HIPAA and Personal Devices	2017-09-05	2017-09-05	U.S.A
6.Leadership: Its Nature and Nurture	2017-08-30	2017-08-30	U.S.A
7.Clinical Trials - Medical Device FDA's Program 2017	2017-08-23	2017-08-24	U.S.A
8.Working with thoroughly Disagreeable, even Dysfunctional Co-workers	2017-08-23	2017-08-23	U.S.A
9.Excel Methods - FDA Device Regulations - 2017	2017-08-22	2017-08-23	U.S.A
10.Letters of Credit are issued under the Customs and Practice 2017	2017-08-21	2017-08-22	U.S.A
11.Medical Devices for Risk Management Techniques 2017	2017-08-21	2017-08-22	U.S.A
12.Employee Engagement: Keeping your Workforce Motivated to Improve Results	2017-08-17	2017-08-17	U.S.A
13.ISO 14971 Hazard Analysis at Medical Device - 2017	2017-08-16	2017-08-17	U.S.A
14.Growing Your Own: The "Truth" About Employee Development	2017-08-15	2017-08-15	U.S.A
15.If it Wasn't Documented it Didn't Happen: Legal & Effective Discipline & Documentation 2017	2017-08-15	2017-08-15	U.S.A
16.California Payroll Processing	2017-08-15	2017-08-15	U.S.A
17.Overtime California Style	2017-08-11	2017-08-11	U.S.A
18.Too Many Flows - How to think about Workflow or Process Flow	2017-08-10	2017-08-10	U.S.A
19.Environmental Monitoring Program at FDA Regulations - 2017	2017-08-09	2017-08-10	U.S.A
20.Laboratory-Developed Tests - Medical devices 2017	2017-08-09	2017-08-10	U.S.A
21.How to Conduct Effective Meetings	2017-08-09	2017-08-09	U.S.A
22.CAPA within a Device Quality System - 2017	2017-08-08	2017-08-09	U.S.A
23.FDA Inspection and Respond to 483 & How to Prepare them - 2017	2017-08-07	2017-08-08	U.S.A
24.Achieving Compliance Excellence - 2017	2017-08-03	2017-08-04	U.S.A
25.Validation Program to a Building from Top to Bottom - 2017	2017-08-03	2017-08-04	U.S.A
26.The New Managers Toolkit to Instant HR Proficiency	2017-08-03	2017-08-03	U.S.A
27.Effective Supplier Qualification Program - 2017	2017-08-02	2017-08-03	U.S.A
28.Cyber Attacks, Beyond Disaster Recovery - 2017	2017-07-31	2017-08-01	U.S.A
29.Your Organization's Culture: If You Don't Get It Right, Nothing Else Matters	2017-07-27	2017-07-27	U.S.A
30.Control Change in Medical Device Engineering - 2017	2017-07-26	2017-07-27	U.S.A
31.Persuasion and Influencing Skills: Cooperation and Collaboration	2017-07-25	2017-07-25	U.S.A
32.Best Practices In Cash Flow Management -By Compliance Global Inc.	2017-07-25	2017-07-25	U.S.A
33.Aseptic Technique Understanding and Cleanroom Behavior - 2017	2017-07-24	2017-07-25	U.S.A
34.Latest FDA Changes to the Process Bullet Proof 510k - 2017	2017-07-24	2017-07-25	U.S.A
35.Exempt vs Non-Exempt and how the FLSA Defines Each	2017-07-24	2017-07-24	U.S.A
36.Using Ratios for Fraud Detection in Corporate Revenue Accounts -By Compliance Global Inc.	2017-07-20	2017-07-20	U.S.A
37.Root Cause Failure Analysis -By Compliance Global Inc	2017-07-20	2017-07-20	U.S.A
38.AML and Beneficial Ownership -By AtoZ Compliance	2017-07-20	2017-07-20	U.S.A
39.Expectations of Regulatory & Validation Master Planning - 2017	2017-07-19	2017-07-20	U.S.A
40.Avoiding the Legal Pitfalls from Screening Applicants	2017-07-19	2017-07-19	U.S.A
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