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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.
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.
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.
You know that each eCTD submission package has to be compliant with ever-changing validation criteria given by EMA - European Medicine Agency.
Uncompliant submission will not pass through regulatory agencies validators, which will result into rejection of the submission and thus a delay in the registration process.
Our Validator is in use on both sides - regulatory agencies and pharmaceutical companies too, which means, you can fully rely on its results.
No software is needed. Validate your sequences directly in the browser, with no extra effort.
Just drag a folder containing your sequence and drop it into upload area.
Uploader pair sequences automatically with another ones of the same dossier.
Upload as many sequences as you wish at once and then validate one by one.
Validator recognizes eCTD or NeeS sequence and runs appropriate validator.
Validator always validated according to the newest validation criteria, but the older are available too.
Results are exportable into PDF format with an explanation and solution of each error.
Validation can be re-run or even manually marked as "passed" if an user have the appropriate permissions.
We're IT and market research professionals, who's been on the market since 2006. We combine deep IT skills with longterm experience and strong knowledge of the pharmaceutical market. BeeCTD was developed for you, to make your regulatory affairs as easy as possible, since we know how precious your time is.
We're located in Bratislava, Prague and Budapest and provide our services in english, german, slovak, czech and hungarian. We cooperate not only with pharmaceutical companies, but with government regulatory agencies as well, which means we know the processes from both sides. Check our main company website at www.ceeor.com, send us an email or give us a call on +421 948 247 270.