You are here: Home

Our eCTD / CTD templates are simple, effective and come ready to use. The templates use Microsoft Word styles for consistency of formatting, and... Read more...

You can now read one of our latest feature articles from our popular monthly newsletter right here. You can have our Regulatory Affairs newsletter... Read more...

iRegulatory's eCTD resource pages - your first port of call for information on eCTD and electronic submissions. This website has the latest news you... Read more...

We have an innovative tool that produces an eCTD readiness report, based on responses given in an online questionnaire which is completed on an... Read more...

Regulatory Consultants and eSubmission Specialists

iRegulatory is a pharmaceutical regulatory affairs consultancy specialising in regulatory submissions. Our regulatory consultants can help you prepare your Marketing Authorisation Applications for submission to regulatory authorities.

We also provide eCTD consultancy services; we can assist you with preparing your application in all eSubmission formats, including eCTD, NeeS and PIM. eCTD submission is one of the core regulatory submissions services our experienced regulatory consultants provide.

If you need assistance with regulatory affairs consultancy or eSubmission projects, please browse our website and contact us, at no obligation.