Regulatory Affairs toolkit for eCTD & NeeS
submissions lifecycle management

The only web-based modular tool for eCTD and NeeS submissions management.

Regulatory affairs suite in web browser

BeeCTD is a full-featured eCTD management solution for pharmaceutical companies and regulatory agencies. Modular architecture and transparent licensing policy allows our users to choose from modules which they want to use – Reader, Compiler, Validator.

SlimEDC makes market research and patient studies seamless

Core features of BeeCTD

01

Reader

Full featured Reader which helps you to get overview over entire lifecycle of dossier containing eCTD and/or NeeS sequences, including baseline submissions while transferring from NeeS to eCTD.

02

Validator

Realtime, fast sequence validator fully compliant with eCTD / NeeS technical specification, incl. best practices criteria. Latest version of eCTD validation criteria always updated, older versions available.

03

Compiler

Get your documents compiled into eCTD compliant format. Use our eCTD compiler tool as a product, which allows you to compile yourself, or as a service - we compile for you on demand.

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portfólio
pfizer
CSL Behring
outsourcing to Ukraine
merck
Amgen
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