eCTD & NeeS Compilation

Biomapas provides full support in Electronic Common Technical Document (eCTD) compilation and submission, as well as Non-eCTD electronic Submissions (NeeS). We use the eCTD Office software. Our team is fully prepared for new requirements and to provide services using the eCTD format. Such a requirement came into force on the 1st of January, 2018.

Full scope eCTD and NeeS services include:

  • A full dossier review and eCTD publishing services;
  • Assessment of old dossiers, gap analysis, updates of the dossier to be compliant and ready for submission;
  • Converting your documents into eCTD/NeeS format;
  • Preparing the Dossiers in eCTD/NeeS for initial submissions/renewals/variations;
  • xml formation required for EAEU;
  • Managing the life cycle of your product(s).

Big Enough To Cover  All Your Needs. Small Enough To Care.

Discover the tailored solutions that Biomapas provides to accelerate your clinical trials and optimize your drug development process.

Clinical Research

Regulatory Affairs

Pharmacovigilance

Medical Information

Big Enough To Cover All Your Needs.
Small Enough To Care.

Discover how Biomapas provides all the support to accelerate your clinical trials and optimize your drug development process.

Clinical Research

Reliable support for every phase of your clinical trial, from recruitment to results.

Pharmacovigilance

Flexible safety monitoring to keep your products compliant and trusted.

Regulatory Affairs

Confidently navigate regulatory challenges with expert support.

Medical Information

Clear, accurate medical information 24/7, tailored for global audiences.

Quality Assurance

Export auditors help identify gaps and close them with actionable solutions.