FAQ
Frequently asked questions
01
In which therapeutic areas is ESPIRA PHARMA most active?Our core focus areas include: Oncology, Rheumatology, Dermatology, Aesthetic Fillers, Metabolic Diseases and Orphan Drugs. Each area reflects our mission to address unmet medical needs through advanced technologies.
02
How does ESPIRA PHARMA ensure quality and compliance across different markets?All our projects comply with EU GMP, ISO, and ICH standards, and our quality management system ensures traceability, transparency, and ethical sourcing throughout every stage — from R&D to commercialization.
03
How can a company become a business partner of ESPIRA PHARMA?Interested companies can send an email to info@espirapharma-sl.com or fill out the Business Collaboration Form on our Partnership page. Once submitted, our Business Development Team will review your profile and reach out to explore collaboration opportunities based on your area of expertise and market presence.
04
What documents or dossiers are required for product registration support?ESPIRA PHARMA assists partners in compiling CTD-formatted registration dossiers including Module 1–5 documentation and stability studies and any other required documents aligned with EMA, FDA, and ICH guidelines.