Siro

SIRO unites two distinct but complementary business units: SIRO Medical Writing: SIRO's global medical writing specialists excel in drug development across various therapeutic areas & product types, bringing deep expertise in regulatory, clinical, & scientific content with extensive experience in medical & scientific writing. Our medical writing services include: • Regulatory Medical Writing: Protocols, Investigator's Brochures (IBs), Clinical Study Reports (CSRs), eCTD modules, PIPs/GIPs, Briefing Books, & more. • Clinical Trial Transparency & Disclosure: Protocol & results registries, document redaction, data anonymization, & lay summaries. • Scientific Publications & Medical Communications: Manuscripts, review articles, consensus guidelines, abstracts, posters, slide decks, & pre/post-launch communication campaigns for pharmaceutical brands. • RWE Solutions: Systematic Literature Reviews (SLRs), Targeted Literature Reviews (TLRs), network meta-analyses, value dossiers, & publications. • DSRM: DSURs, RMPs, SUSAR LLs, PBRERs, PADERs, ACOs, & PSURs. • Plain Language Summaries (PLSs) Our vision is to lead medical writing by leveraging expertise, technology, & global reach for unparalleled solutions. SIRO Clinpharm: SIRO is a trusted FSP supporting global pharmaceutical & IT firms across Clinical Development, Drug Safety, & Regulatory services. We provide specialized talent & flexible workforce solutions tailored to your specific needs. Key functional areas: • Clinical Operations • Project Management • Clinical Monitoring • Start-up Services • Clinical Data Management • Biostatistics & Statistical Programming • IT Key differentiators: Industry expertise with tailored solutions for pharma, biotech, CROs, IT, & agencies; global hiring across 150+ countries; niche talent access; a dual staffing approach blending internal pools with custom recruitment; & swift, reliable deployment for on-time resource delivery. Visit us: |