Navatio Pharma
Navatio Pharma Solutions is a leading global contract research organization specializing in pharmacovigilance, materiovigilance, medical writing, regulatory affairs, and QPPVs. They are dedicated to advancing drug and medical device safety by delivering compliant, high-quality solutions tailored to pharmaceutical, biotech, and healthcare organizations worldwide.
Industries
Nr. of Employees
small (1-50)
Navatio Pharma
Services
Comprehensive drug safety services including case processing, literature monitoring, aggregate reporting, signal detection, risk management planning, and audits.
Implementation and ongoing maintenance of PV systems and processes tailored to regulatory frameworks and client needs.
Continuous medical information support for clinical and safety inquiries and adverse event reporting, available 24/7.
Safety monitoring and reporting services tailored for veterinary medicinal products.
Adverse effect monitoring and safety management for cosmetic products to support consumer safety and compliance.
Preparation of regulatory and clinical documents including safety narratives, clinical study documents, and submission-ready materials.
Comprehensive drug safety services including case processing, literature monitoring, aggregate reporting, signal detection, risk management planning, and audits.
Implementation and ongoing maintenance of PV systems and processes tailored to regulatory frameworks and client needs.
Continuous medical information support for clinical and safety inquiries and adverse event reporting, available 24/7.
Safety monitoring and reporting services tailored for veterinary medicinal products.
Adverse effect monitoring and safety management for cosmetic products to support consumer safety and compliance.
Preparation of regulatory and clinical documents including safety narratives, clinical study documents, and submission-ready materials.
Expertise Areas
- Pharmacovigilance and drug safety
- Signal detection and risk management
- Medical information and case management
- Regulatory affairs and dossier submissions
Key Technologies
- ICSR management systems
- Literature surveillance and screening
- Signal detection methodologies
- Aggregate safety report generation
News & Updates
Literature Monitoring serves as a crucial component in pharmacovigilance to ensure drug safety and regulatory compliance.
Pharmaceutical companies navigate an increasingly intricate regulatory landscape where drug safety and compliance remain paramount.
Rare diseases, also known as orphan diseases, affect fewer than 1 in 2,000 individuals in Europe, impacting approximately 27 to 36 million.
Literature Monitoring serves as a crucial component in pharmacovigilance to ensure drug safety and regulatory compliance.
Pharmaceutical companies navigate an increasingly intricate regulatory landscape where drug safety and compliance remain paramount.
Rare diseases, also known as orphan diseases, affect fewer than 1 in 2,000 individuals in Europe, impacting approximately 27 to 36 million.