| Conference | Deadline | Date | Country |
| 1.In the Workplace: Training for Managers and Supervisors | 2014-07-22 | 2014-07-24 | U.S.A |
| 2.5 Reasons your Hiring Practices may be Illegal and Ineffective | 2014-07-22 | 2014-07-23 | U.S.A |
| 3.How to Conduct a Hazard Analysis/Risk Assessment | 2014-07-22 | 2014-07-22 | U.S.A |
| 4.A 60 minutes webinar on Introduction to Nano-materials | 2014-07-22 | 2014-07-22 | U.S.A |
| 5."6-hr Virtual Seminar: Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry" | 2014-07-22 | 2014-07-22 | U.S.A |
| 6."6-hr Virtual Seminar: Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry" | 2014-07-22 | 2014-07-22 | U.S.A |
| 7.6-hr Virtual Seminar: Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry | 2014-07-22 | 2014-07-22 | U.S.A |
| 8."6-hr Virtual Seminar: Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry" | 2014-07-22 | 2014-07-22 | U.S.A |
| 9.Live Webinar-6-hr Virtual Seminar: Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry | 2014-07-22 | 2014-07-22 | U.S.A |
| 10.Online Conference-6-hr Virtual Seminar: Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry | 2014-07-22 | 2014-07-22 | U.S.A |
| 11.Introduction to Nanomaterials - Identifying and Managing Health, Safety and Environmental Risks | 2014-07-22 | 2014-07-22 | U.S.A |
| 12.2014 International Conference on Logistics, Informatics and Services Sciences | 2014-07-23 | 2014-07-26 | U.S.A |
| 13."CAPA Training and Causes of Warning Letters due to Lack of Comprehension" | 2014-07-23 | 2014-07-23 | U.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" | 2014-07-23 | 2014-07-23 | U.S.A |
| 15."CAPA Training and Causes of Warning Letters due to Lack of Comprehension" | 2014-07-23 | 2014-07-23 | U.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" | 2014-07-23 | 2014-07-23 | U.S.A |
| 17.CAPA Training and Causes of Warning Letters due to Lack of Comprehension | 2014-07-23 | 2014-07-23 | U.S.A |
| 18.Design History File (DHF), the Device Master Record (DMR) and the Device History Record (DHR) – Principles on Lean Documents and Lean Configuration | 2014-07-23 | 2014-07-23 | U.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" | 2014-07-23 | 2014-07-23 | U.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" | 2014-07-23 | 2014-07-23 | U.S.A |
| 21."CAPA Training and Causes of Warning Letters due to Lack of Comprehension" | 2014-07-23 | 2014-07-23 | U.S.A |
| 22.Live Webinar-CAPA Training and Causes of Warning Letters due to Lack of Comprehension | 2014-07-23 | 2014-07-23 | U.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 Configuration | 2014-07-23 | 2014-07-23 | U.S.A |
| 24.3rd International Conference on Management, Leadership and Governance | 2014-07-24 | 2015-02-12 | New Zealand |
| 25."How to Host Regulatory Audits (FDA, EU and Health Canada)" | 2014-07-24 | 2014-07-24 | U.S.A |
| 26."SOP and FDA Compliance" | 2014-07-24 | 2014-07-24 | U.S.A |
| 27."How to Host Regulatory Audits (FDA, EU and Health Canada)" | 2014-07-24 | 2014-07-24 | U.S.A |
| 28."SOP and FDA Compliance" | 2014-07-24 | 2014-07-24 | U.S.A |
| 29.How to Host Regulatory Audits (FDA, EU and Health Canada) | 2014-07-24 | 2014-07-24 | U.S.A |
| 30.SOP and FDA Compliance | 2014-07-24 | 2014-07-24 | U.S.A |
| 31."SOP and FDA Compliance" | 2014-07-24 | 2014-07-24 | U.S.A |
| 32."How to Host Regulatory Audits (FDA, EU and Health Canada)" | 2014-07-24 | 2014-07-24 | U.S.A |
| 33."SOP and FDA Compliance" | 2014-07-24 | 2014-07-24 | U.S.A |
| 34.Live Webinar-How to Host Regulatory Audits (FDA, EU and Health Canada) | 2014-07-24 | 2014-07-24 | U.S.A |
| 35.Live Webinar-SOP and FDA Compliance | 2014-07-24 | 2014-07-24 | U.S.A |
| 36.Online Conference-How to Host Regulatory Audits (FDA, EU and Health Canada) | 2014-07-24 | 2014-07-24 | U.S.A |
| 37.Online Conference-SOP and FDA Compliance | 2014-07-24 | 2014-07-24 | U.S.A |
| 38.How to Host Regulatory Audits (FDA, EU and Health Canada) | 2014-07-24 | 2014-07-24 | U.S.A |
| 39.SOP and FDA Compliance | 2014-07-24 | 2014-07-24 | U.S.A |
| 40.Marketing to Medicare or Medicaid Beneficiaries - What You Can and Cannot Do | 2014-07-24 | 2014-07-24 | U.S.A |
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