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15/05/2014 Annual Life Sciences Conference and Training. 2014/01/24 Common Electronic Submissions Gateway (CESG) to send regulatory transactions to Health Canada. 26/02/2014 TGA reaches Electronic-only (eCTD) submissions milestone. REMINDER: EMA gateway made mandatory. 17/02/2014 FDA Guidance Agenda: New and Revised Draft Guidances CDER is Planning to Publish During Calendar Year 2014. Join our mailing list. Qdossier: flexible eRegulatory solutions. Organising eCTD structures and lifecycles.

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15/05/2014 Annual Life Sciences Conference and Training. 2014/01/24 Common Electronic Submissions Gateway (CESG) to send regulatory transactions to Health Canada. 26/02/2014 TGA reaches Electronic-only (eCTD) submissions milestone. REMINDER: EMA gateway made mandatory. 17/02/2014 FDA Guidance Agenda: New and Revised Draft Guidances CDER is Planning to Publish During Calendar Year 2014. Join our mailing list. Qdossier: flexible eRegulatory solutions. Organising eCTD structures and lifecycles.
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Qdossier - First time right | qdossier.com Reviews

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15/05/2014 Annual Life Sciences Conference and Training. 2014/01/24 Common Electronic Submissions Gateway (CESG) to send regulatory transactions to Health Canada. 26/02/2014 TGA reaches Electronic-only (eCTD) submissions milestone. REMINDER: EMA gateway made mandatory. 17/02/2014 FDA Guidance Agenda: New and Revised Draft Guidances CDER is Planning to Publish During Calendar Year 2014. Join our mailing list. Qdossier: flexible eRegulatory solutions. Organising eCTD structures and lifecycles.

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ECTDconsultancy was founded in January 2006 by Hans van Bruggen. We are located in Waalwijk, The Netherlands. Our consultants possess extensive previous experience of Drug Development and electronic Regulatory Submissions, including:. Preparation of the first eCTD on a New Chemical Entity worldwide. Preparation and submission of the first eCTD for a Centralised Procedure in the EU. Design and implementation of Global Document Management Solutions. Design and implementation of company eCTD strategies.

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eCTDconsultancy - The Science Of Submissions

http://www.ectd-consultancy.nl/content/ectd_consultancy_about.asp

ECTDconsultancy was founded in January 2006 by Hans van Bruggen. We are located in Waalwijk, The Netherlands. Our consultants possess extensive previous experience of Drug Development and electronic Regulatory Submissions, including:. Preparation of the first eCTD on a New Chemical Entity worldwide. Preparation and submission of the first eCTD for a Centralised Procedure in the EU. Design and implementation of Global Document Management Solutions. Design and implementation of company eCTD strategies.

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eCTDconsultancy - The Science Of Submissions

http://www.ectd-consultancy.com/content/ectd_consultancy_about.asp

ECTDconsultancy was founded in January 2006 by Hans van Bruggen. We are located in Waalwijk, The Netherlands. Our consultants possess extensive previous experience of Drug Development and electronic Regulatory Submissions, including:. Preparation of the first eCTD on a New Chemical Entity worldwide. Preparation and submission of the first eCTD for a Centralised Procedure in the EU. Design and implementation of Global Document Management Solutions. Design and implementation of company eCTD strategies.

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15/05/2014 Annual Life Sciences Conference and Training. 2014/01/24 Common Electronic Submissions Gateway (CESG) to send regulatory transactions to Health Canada. 26/02/2014 TGA reaches Electronic-only (eCTD) submissions milestone. REMINDER: EMA gateway made mandatory. 17/02/2014 FDA Guidance Agenda: New and Revised Draft Guidances CDER is Planning to Publish During Calendar Year 2014. Join our mailing list. Qdossier: flexible eRegulatory solutions. Organising eCTD structures and lifecycles.

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