Presented by Antoinette Azevedo, e-SubmissionsSolutions.com at Documentation and Training Life Sciences, June 23-26, 2008 in Indianapolis.Life sciences regulatory authorities…

Brief description of the documents required for ANDA submission

1.Summary23.06.2012 17:53:08Differences exist between documents.New Document:Old Document:Q & A for EMA eSubmission Gateway_22062012 Q & A for EMA eSubmission Gateway_1804201211…

CMDh BPG on the use of the eCTD in the MRP/DCP November 2011 Page 1/22 CMDh BEST PRACTICE GUIDE ON THE USE OF THE ELECTRONIC COMMON TECHNICAL DOCUMENT (eCTD) IN THE MUTUAL…

Overview of the Role of the Regulatory Agencies and of Regulations in Product Development for Pharma Remit of EMA/FDA Objectives/Agenda The role of regulation History of…

1.Overview of Services and Value Propositions2010 2. Q: Besides Being Blockbuster Products,What Do These Have in Common?$4.4B*$1.5B*Drug-eluting coronary stent $3.8B* $3.6B*…

Prezentace aplikace PowerPoint Partner in Life Science Industry www.asamuel.eu www.asamuel.eu Partner in Life Science Industry Who we are? Team of specialised experts All…