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ConferenceDeadline DateCountry
1.In the Workplace: Training for Managers and Supervisors2014-07-222014-07-24U.S.A
2.5 Reasons your Hiring Practices may be Illegal and Ineffective2014-07-222014-07-23U.S.A
3.How to Conduct a Hazard Analysis/Risk Assessment2014-07-222014-07-22U.S.A
4.A 60 minutes webinar on Introduction to Nano-materials2014-07-222014-07-22U.S.A
5."6-hr Virtual Seminar: Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry"2014-07-222014-07-22U.S.A
6."6-hr Virtual Seminar: Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry"2014-07-222014-07-22U.S.A
7.6-hr Virtual Seminar: Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry2014-07-222014-07-22U.S.A
8."6-hr Virtual Seminar: Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry"2014-07-222014-07-22U.S.A
9.Live Webinar-6-hr Virtual Seminar: Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry2014-07-222014-07-22U.S.A
10.Online Conference-6-hr Virtual Seminar: Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry2014-07-222014-07-22U.S.A
11.Introduction to Nanomaterials - Identifying and Managing Health, Safety and Environmental Risks2014-07-222014-07-22U.S.A
12.2014 International Conference on Logistics, Informatics and Services Sciences2014-07-232014-07-26U.S.A
13."CAPA Training and Causes of Warning Letters due to Lack of Comprehension"2014-07-232014-07-23U.S.A
14."Design History File (DHF), the Device Master Record (DMR) and the Device History Record (DHR) – Principles on Lean Documents and Lean Configuration"2014-07-232014-07-23U.S.A
15."CAPA Training and Causes of Warning Letters due to Lack of Comprehension"2014-07-232014-07-23U.S.A
16."Design History File (DHF), the Device Master Record (DMR) and the Device History Record (DHR) – Principles on Lean Documents and Lean Configuration"2014-07-232014-07-23U.S.A
17.CAPA Training and Causes of Warning Letters due to Lack of Comprehension2014-07-232014-07-23U.S.A
18.Design History File (DHF), the Device Master Record (DMR) and the Device History Record (DHR) – Principles on Lean Documents and Lean Configuration2014-07-232014-07-23U.S.A
19."Design History File (DHF), the Device Master Record (DMR) and the Device History Record (DHR) – Principles on Lean Documents and Lean Configuration"2014-07-232014-07-23U.S.A
20."Design History File (DHF), the Device Master Record (DMR) and the Device History Record (DHR) – Principles on Lean Documents and Lean Configuration"2014-07-232014-07-23U.S.A
21."CAPA Training and Causes of Warning Letters due to Lack of Comprehension"2014-07-232014-07-23U.S.A
22.Live Webinar-CAPA Training and Causes of Warning Letters due to Lack of Comprehension2014-07-232014-07-23U.S.A
23.online Conference-Design History File (DHF), the Device Master Record (DMR) and the Line Device History Record (DHR) – Principles on Lean Documents and Lean Configuration2014-07-232014-07-23U.S.A
24.3rd International Conference on Management, Leadership and Governance2014-07-242015-02-12New Zealand
25."How to Host Regulatory Audits (FDA, EU and Health Canada)"2014-07-242014-07-24U.S.A
26."SOP and FDA Compliance"2014-07-242014-07-24U.S.A
27."How to Host Regulatory Audits (FDA, EU and Health Canada)"2014-07-242014-07-24U.S.A
28."SOP and FDA Compliance"2014-07-242014-07-24U.S.A
29.How to Host Regulatory Audits (FDA, EU and Health Canada)2014-07-242014-07-24U.S.A
30.SOP and FDA Compliance2014-07-242014-07-24U.S.A
31."SOP and FDA Compliance"2014-07-242014-07-24U.S.A
32."How to Host Regulatory Audits (FDA, EU and Health Canada)"2014-07-242014-07-24U.S.A
33."SOP and FDA Compliance"2014-07-242014-07-24U.S.A
34.Live Webinar-How to Host Regulatory Audits (FDA, EU and Health Canada)2014-07-242014-07-24U.S.A
35.Live Webinar-SOP and FDA Compliance2014-07-242014-07-24U.S.A
36.Online Conference-How to Host Regulatory Audits (FDA, EU and Health Canada)2014-07-242014-07-24U.S.A
37.Online Conference-SOP and FDA Compliance2014-07-242014-07-24U.S.A
38.How to Host Regulatory Audits (FDA, EU and Health Canada)2014-07-242014-07-24U.S.A
39.SOP and FDA Compliance2014-07-242014-07-24U.S.A
40.Marketing to Medicare or Medicaid Beneficiaries - What You Can and Cannot Do2014-07-242014-07-24U.S.A
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