Optimally Reuse Regulatory Documents Across Dossiers

April 18, 2013 - PRLog -- Maximising efficiency, delivering costs reductions, increasing team effectiveness, and  optimising resources are key goals within the pharmaceutical industry. Whether teams are launching simultaneous submissions, maximising profits with old product launches, or taking new products into new countries; information re-use across paper, Non-eCTD electronic Submissions (NeeS) and electronic Common Technical Document (eCTD) submissions is seen as an essential part of saving time when creating new submissions.

SMi's masterclass led by eCTDconsultancy involves paradigms, new concepts, in-depth sessions, analysis, and active discussions to show the way to successful strategy and achievement of these goals.

Attendees will benefit from:
• Understand how you can improve transparency in the regulatory data
• Improve the efficiency in business processes, including reuse of regulatory documents across dossiers.
• Learn from expert advice and apply to your business to maximise effectiveness

Those who wish to attend please contact Contact Fateja Begum on +44 (0) 20 7827 6184 or fbegum@smi-online.co.uk. For more information please visit www.smi-online.co.uk/regulatory-documents.asp

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About the host
Hans van Bruggen is Director of eCTDconsultancy. He has an MSc in Pharmaceutical Medicine from the University of Surrey (UK) and has worked within, or for, the pharmaceutical industry for more than 30 years in Global or European Headquarters. He has gained a wealth of experience and a comprehensive view on what is needed to evaluate the benefit/risk ratio of drugs for patients and healthy volunteers.