NeeS, VNeeS and eCTD Consultancy

Are you a pharmaceutical company looking to manage your NeeS / eCTD submissions, for EMA or Swiss, from content planning to final compilation and lifecycle management?

With more than 30 years of experience in pharmaceutical industry we can help you understand and manage your eSubmissions with ease.

eCTD Office Support / eChecker (VNeeS Validator) Requests

If you would like more info on eCTD Office or eChecker (VNeeS Validator) please complete the contact form:


* please ensure a valid Company name or a URL of a Company web site.





Note: we keep the right not to answer your query if we cannot find your Company on the Internet or if you have specified a "yahoo", "hotmail", "aol" or "gmail" (and alike) email address.

Direct Contact

If you would like to contact us directly, please use the following contact information:

Support, Trainings, Queries:
willem@ectdoffice.com

eCTD Office IT support:
zarko@ectdoffice.com

eChecker (VNeeS Validator) support:
echecker@ectdoffice.com

Bredestraat 14
3090 Overijse (Bruxelles)
Belgium

Help and FAQ

The eCTD Office Help & FAQ page lists answers to frequently asked questions about installing, configuring and using eCTD Office products.

About Pharmaceutical Regulatory and Software [Support, Training]

With more than 30 years of experience PRS, Pharmaceutical Regulatory and Software, offers a full range of expert technical consultation and training in the area of the Pharmaceutical Regulatory.

Close association with a broad network of Expert Software Developers allows advice in developing appropriated software tools for Pharmaceutical Consultancy and Industries.

About Mono Software [Software development, IT support]

Mono Software Ltd. creates and distributes custom software applications and knowledge management solutions. Founded in 1996, the company has an innovative and creative approach to software development, producing cutting-edge solutions while respecting budget and time requirements.

Due to its competency, Mono Software Ltd. has been chosen for software development projects by partners from Croatia, USA, Ireland, France, Switzerland, Belgium, and other countries. Mono products are used in more than 60 countries on all continents.

eCTD Office
helps you do the job...

eCTD Office applications are being used by pharma companies and pharmaceutical consultancy companies all over Europe (France, The Netherlands, Belgium, Poland, Spain, Czech Republic, Germany, UK, Bulgaria, Ireland, ...).

User Experience

"eCTD Office programs are almost self-explaining. Working with it is really simple, even for complete registration dossiers. Finally, the possibility to do the checking of the complete file before submission provides certainty and relief for not being rejected. Besides the program itself the continuous service (questions, immediate problem-solving) is highly appreciated."

- F. Doperé - P. Ramoisiaux
Regulatory Affairs - S.A. Meda Pharma N.V. Brussels, Belgium

"One of the great advantages of eCTD Office is that you don't have to search and delete the empty folders manually. Another advantage is that the folder and file names are corrected automatically - a big bonus because your submission can be refused for wrong naming ! And if you have a series of submissons for one product, the new history template is a great time saver, because we don't have to create a new PDF for each submission."

- Hildegarde Baeken
Regulatory Affairs Assistant Ratiopharm Belgium nv/sa

eCTD Office has been partially funded by the European Union

Development of eCTD Office has been partially funded by the European Union.