Regulatory Affairs professional with 2+ years of experience in pharmaceutical dossier preparation and CTD/ACTD/eCTD document formatting.
I specialize in regulatory document structuring, PDF bookmarking, hyperlinking, pagination, table of contents creation, and submission-ready dossier compilation.
I have practical experience working with documentation aligned to guidelines from the Central Drugs Standard Control Organization (CDSCO), US FDA, and EMA.
If you need professional, clean, and regulatory-ready formatting support — I’m here to help.... Lee más