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ConferenceDeadline DateCountry
1.International Conference on Innovative & Sustainable Management Practices: A Global Perspective2014-11-102015-01-23India
2.International Conference on Advanced Engineering and Technology (ICAET 2014) in Incheon2014-11-282014-12-20South Korea
3.Third International conference on Parallel, Distributed Computing and Applications (IPDCA 2014)2014-11-012014-12-27India
4.Sixth International Conference on Applications of Graph Theory in Wireless Ad hoc Networks & Sensor Networks (GRAPH-HOC 2014)2014-11-012014-12-27India
5.Sixth International Conference on Networks & Communications (NETCOM - 2014)2014-11-012014-12-27India
6.The 3rd Genetics and Genomics Conference (GC 2014)2014-11-152014-12-26China
7.24th IEEE International Conference on Enabling Technologies: Infrastructure for Collaborative Enterprises2014-11-212015-06-15Cyprus
8.The 3rd Asia-Pacific Conference on Management and Business2015-03-202015-06-27South Korea
9.2nd Annual International Conference on Accounting and Finance - 20152015-03-312015-05-25Sri Lanka
10.International Conference on Advanced Materials, Mechanical Engineering and Technology (ICAMMET 2015)2015-03-062015-03-21China
11.International Conference on Applied Mechanics, Materials and Structural Engineering (ICAMMSE 2015)2015-01-142015-01-25China
12.The 2nd Conf. on Catalysis (ICC 2014)2014-11-152014-12-26China
13.IEEE VTC2015-Spring Recent Results & Workshops2014-12-172015-05-11U.K.
14.Conference in Maui, Hawaii Life , Worthshop 42014-12-112014-12-11U.S.A
15.US, EU and Japan GMP Requirements: Practical ICH Area Differences, Healthcare Authority Inspection Focus2014-11-102014-11-10U.S.A
16.DEC in Action: Best Practices for Dispute Resolution Teaching and Learning2014-11-202014-11-20Hong Kong
17.CALL FOR PAPERS: Journal of Law, Technology and Public Policy2014-12-312014-12-31Hong Kong
18.Online conference 21 CFR Part 11 Add-On Inspections by the FDA2014-11-202014-11-20U.S.A
19.Online conference Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration2014-11-192014-11-19U.S.A
20.Online conference Internet Issues for FDA-Regulated Industry – A Review of Issues Involving Social Media2014-11-182014-11-18U.S.A
21.Online conference Best Practices for Quality Risk Management for Pharmaceutical Industry2014-11-132014-11-13U.S.A
22.Online conference Meet the New, Tougher FDA Expectations2014-11-122014-11-12U.S.A
23.Online conference US, EU and Japan GMP Requirements: Practical ICH Area Differences, Healthcare Authority Inspection Focus2014-11-102014-11-10U.S.A
24.Online conference 21 CFR Part 820 Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration2014-11-072014-11-07U.S.A
25.Online conference Patient Rights and the HIPAA Privacy Officer - Meeting Patient Desires and Avoiding Penalties2014-11-042014-11-04U.S.A
26.Online conference Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs2014-11-032014-11-03U.S.A
27.Online conference Secrets of Successful Medical Device Product Development Process2014-10-302014-10-30U.S.A
28.Online conference Hosting Regulatory Inspections2014-10-302014-10-30U.S.A
29.Online conference Implementing Adequate CAPA and Design Control Procedures2014-10-282014-10-28U.S.A
30.Special Considerations during Medical Device Design: Dos and Don'ts2014-11-262014-11-26U.S.A
31.21 CFR Part 11 Add-On Inspections by the FDA2014-11-202014-11-20U.S.A
32.Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration2014-11-192014-11-19U.S.A
33.Internet Issues for FDA-Regulated Industry – A Review of Issues Involving Social Media2014-11-182014-11-18U.S.A
34.Bioterrorism and Food Security-A Cultural Conundrum2014-11-142014-11-14U.S.A
35.Meet the New, Tougher FDA Expectations2014-11-122014-11-12U.S.A
36.21 CFR Part 820 Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration2014-11-072014-11-07U.S.A
37.Patient Rights and the HIPAA Privacy Officer - Meeting Patient Desires and Avoiding Penalties2014-11-042014-11-04U.S.A
38.Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs2014-11-032014-11-03U.S.A
39.Secrets of Successful Medical Device Product Development Process2014-10-302014-10-30U.S.A
40.Hosting Regulatory Inspections2014-10-302014-10-30U.S.A
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