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ConferenceDeadline DateCountry
1.Live webinar Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry2015-01-272015-01-27U.S.A
2.Live webinar How to Host Regulatory Audits (FDA, EU and Health Canada)2015-01-212015-01-21U.S.A
3.Live webinar DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions2015-01-212015-01-21U.S.A
4.Live webinar NAFTA Rules of Origin and Documentation2015-01-202015-01-20U.S.A
5.Live webinar Drug Master Files - Understanding and Meeting Your Global Regulatory and Processing Responsibilities2015-01-202015-01-20U.S.A
6.Live webinar Effective Root Cause Analysis: The Key to an effective corrective actions system2015-01-152015-01-15U.S.A
7.Live webinar Creation of DHFs, DMRs, and DHRs utilizing the principles of Lean Documents and Lean Configuration2015-01-142015-01-14U.S.A
8.Live webinar FDA’s Part 11 – Enforcement Trends and Affordable Steps to Take Today2015-01-132015-01-13U.S.A
9.Live webinar The New HIPAA Audit Program for 2015: How to Prepare and Avoid Penalties by complince2go2015-01-132015-01-13U.S.A
10.Best Practices to Prevent Fraud: Understanding the Trends, Threats and Strategies2015-01-132015-01-13U.S.A
11.The Evaluation Trap: Why Your Performance Appraisal System is Most Likely to Be Used Against You in Court and What to Do Instead2015-01-122015-01-12U.S.A
12.The Tools the HR Executive Needs to Build an Internal Complaint System that Gets Results!2015-01-122015-01-12U.S.A
13.Implementing Operations Risk Management within an ERM Framework2015-01-092015-01-09U.S.A
14.Understanding USERRA: How to Balance Respect for Military Service with the Realities of the Workplace2015-01-092015-01-09U.S.A
15.Gaining and Re-Establishing Control of Your Cleanroom2015-01-092015-01-09U.S.A
16.OSHA Recordkeeping for 2015: Beyond the OSHA 300 Summary2015-01-092015-01-09U.S.A
17.Bank Secrecy Act (BSA) Audit Best Practices2015-01-082015-01-08U.S.A
18.Patient Protection and Affordable Care Act Compliance for Large Employers2015-01-082015-01-08U.S.A
19.FDA Bioterrorism Act Food Facility Registration - Public Health Security and Bioterrorism Preparedness2015-01-082015-01-08U.S.A
20.The 4th Asian Conference on Civil, Material and Environmental Sciences2015-05-152015-08-25Japan
21.Asia-Pacific Conference on Engineering and Applied Science (APCEAS)2015-05-152015-08-25Japan
22.The 2nd International Conference on Sensors and Materials Manufacturing Science 20152015-01-052015-01-17France
23.International Conference on Transportation Systems and Industry Research2015-02-102015-06-19China
24.2015 Conference on Advances in Prevention and Treatment of Cancer (CAPTC 2015)2015-02-042015-03-18China
25.International Conference on Mechanisms and Nanosystems2015-02-102015-06-19China
26.2015 Conference on Tissue Engineering and Regenerative Medicine (CTERM 2015)2015-02-042015-03-18China
27.2015 International Conference on Electrical Systems and Advanced Manufacturing2015-02-102015-06-19China
28.GAMP® 5 as applied to FDA software validation - strategies to avoid warning letters2015-01-212015-01-21U.S.A
29.International Conference on Modern Greek Language, Literature, History and Civilization2015-03-152015-04-16Poland
30.International Research Conference on Science, Management and Engineering 20152014-12-262015-01-28United Arab Emirates
31.Effective Behavioral Interviewing: Seeing Past the Surface2015-01-222015-01-22U.S.A
32.21 CFR Part 820 Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration2015-01-282015-01-28U.S.A
33.Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry2015-01-272015-01-27U.S.A
34.FDA Recordkeeping Requirements2015-01-272015-01-27U.S.A
35.How to Host Regulatory Audits (FDA, EU and Health Canada)2015-01-222015-01-22U.S.A
36.DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions2015-01-212015-01-21U.S.A
37.Drug Master Files - Understanding and Meeting Your Global Regulatory and Processing Responsibilities2015-01-202015-01-20U.S.A
38.NAFTA Rules of Origin and Documentation2015-01-202015-01-20U.S.A
39.Effective Root Cause Analysis: The Key to an effective corrective actions system2015-01-152015-01-15U.S.A
40.Creation of DHFs, DMRs, and DHRs utilizing the principles of Lean Documents and Lean Configuration2015-01-142015-01-14U.S.A
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