Diamond BioPharm Limited’s eCTD Electronic Publishing Service Has Arrived
January 2010, when eCTD becomes a reality for your submissions, is fast approaching. Regulatory Authorities across Europe are already encouraging the submission of a fully electronic CTD for centralised, decentralised and MRP submissions, some with an incentive of reduced fees.
To meet your needs Diamond BioPharm Limited has installed, validated and is ready to utilise its fully integrated, confidential and state-of-the-art e-Publishing software. We can therefore assure you of and offer you our high-quality service for e-publishing your dossier and/or converting your legacy documents into eCTD format.
Publishing a dossier as a fully functional eCTD is an important end result. The art to the eCTD is creating submission ready documents from the outset, fully compliant with ICH standards.
Diamond BioPharm Limited can help you through the whole process by:
- creating your submission-ready documents using our world class templates which automatically build in the functionality by use of a simple and user-friendly toolbar.
- transposing your word documents onto the templates, both new and legacy documents
- maintaining and updating your eCTD, making life cycle management simple and quick
- producing for you the very best eCTD dossier at competitive costs
Our eCTD process is managed by a dedicated team and supported by our regulatory experts, to ensure your deadlines and requirements are fully met.