Matraz Innova
Consulting firm focused on the pharmaceutical, biotech and medical device sectors offering end-to-end services across clinical development (CRO), regulatory affairs, pharmacovigilance, medical affairs, commercial development, market analysis and digital transformation. Operates from Spain with stated presence in Madrid and Sevilla and provides consulting, managed services and project-based implementations.
Industries
Nr. of Employees
small (1-50)
Matraz Innova
Madrid, Distrito Especial, Colombia, South America
Products
Community podcast for life science professionals
Podcast featuring interviews with professionals across clinical operations, regulatory, pharmacovigilance, quality and related areas in the life sciences sector. Episodes available on Spotify.
Community podcast for life science professionals
Podcast featuring interviews with professionals across clinical operations, regulatory, pharmacovigilance, quality and related areas in the life sciences sector. Episodes available on Spotify.
Services
End-to-end clinical trial support including protocol design, site selection, monitoring, patient recruitment, data management, SAE handling and statistical reporting.
Regulatory strategy development, dossier preparation and submission, management of variations and maintenance of regulatory records for multiple jurisdictions.
Implementation and operation of PV systems, adverse event reporting, preparation of PSURs and maintenance of safety databases.
KOL mapping and engagement, advisory board facilitation, development of scientific and educational materials, and CME program design.
Qualitative and quantitative market research, competitor benchmarking and segmentation reports with actionable recommendations.
Design and delivery of sales training courses, workshops and value-proposition development to improve commercial effectiveness and prospecting.
End-to-end clinical trial support including protocol design, site selection, monitoring, patient recruitment, data management, SAE handling and statistical reporting.
Regulatory strategy development, dossier preparation and submission, management of variations and maintenance of regulatory records for multiple jurisdictions.
Implementation and operation of PV systems, adverse event reporting, preparation of PSURs and maintenance of safety databases.
KOL mapping and engagement, advisory board facilitation, development of scientific and educational materials, and CME program design.
Qualitative and quantitative market research, competitor benchmarking and segmentation reports with actionable recommendations.
Design and delivery of sales training courses, workshops and value-proposition development to improve commercial effectiveness and prospecting.
Expertise Areas
- Clinical trial management
- Pharmacovigilance and safety surveillance
- Regulatory affairs and dossier management
- Medical affairs and KOL engagement
Key Technologies
- Clinical data management systems
- Pharmacovigilance safety databases
- Statistical analysis for clinical studies
- Regulatory dossier preparation workflows
News & Updates
Podcast series for professionals in the life sciences community covering clinical, regulatory, pharmacovigilance, quality and related topics.
Podcast series for professionals in the life sciences community covering clinical, regulatory, pharmacovigilance, quality and related topics.