Provider of Premier Documents

This is Illyria... provider of premier documents to the biopharmaceutical industry.  Illyria creates documents that stand alone or fit directly into your Common Technical Document-compliant IND, NDA, or BLA.

Illyria also supports your organization’s infrastructure by producing ICH-compliant templates, SOPs, and work practice guidelines, and by managing and developing medical writing groups.

Illyria’s expertise includes:

•Clinical documents—study reports, protocols and amendments, investigator brochures, patient safety narratives

•Nonclinical documents—technical reports, integrated pharmacology, pharmacokinetic, and immunogenicity reports

•Quality documents—stability studies, assay validation reports

•CTD Module 2 overviews and summaries, and ISSs and ISEs

•Pre-meeting packages, orphan drug applications, data safety monitoring board charters

•Journal articles, white papers, text for scientific posters, and corporate communication policies