IntuVigilance
IntuVigilance is a pharmacovigilance company dedicated to providing innovative, thorough solutions in drug safety and pharmacovigilance. They focus on compliance, quality assurance, safety, and risk management, with a strong emphasis on strategic alliances and long-term partnerships within the industry. Their services include QPPV services, literature monitoring, pharmacovigilance system oversight, drug safety operations, and regulatory intelligence, supported by ISO certifications and a comprehensive quality management system.
Industries
Nr. of Employees
small (1-50)
IntuVigilance
Rickmansworth, Hertford, United Kingdom, Europe
Products
Regulatory intelligence database (platform)
A regulatory collection system offering country-specific pharmacovigilance reporting guidelines and legislative updates to support compliant safety reporting.
Regulatory-ready safety report deliverables (R3-ready)
Production of safety reports formatted to meet regulatory submission requirements and expedite review by authorities.
Regulatory intelligence database (platform)
A regulatory collection system offering country-specific pharmacovigilance reporting guidelines and legislative updates to support compliant safety reporting.
Regulatory-ready safety report deliverables (R3-ready)
Production of safety reports formatted to meet regulatory submission requirements and expedite review by authorities.
Services
Provision of EU and local Qualified Person Responsible for Pharmacovigilance and coordination of local PV contacts to maintain regulatory presence and oversight.
Access to a regulatory intelligence database providing precise, country-specific pharmacovigilance reporting guidelines and updates.
Global case processing and rapid reporting services using a SaaS safety database with integrated gateways to regulatory authorities.
Centralized weekly literature screening performed by qualified PV professionals to identify and assess safety signals and publications.
Development and maintenance of PSMFs, RMPs, PSURs, DSURs, PSSFs and other PV documentation to meet global and local regulatory requirements.
Gap analyses, development, implementation and maintenance of SOPs and Quality Management Systems aligned with GxP and ISO standards.
Provision of EU and local Qualified Person Responsible for Pharmacovigilance and coordination of local PV contacts to maintain regulatory presence and oversight.
Access to a regulatory intelligence database providing precise, country-specific pharmacovigilance reporting guidelines and updates.
Global case processing and rapid reporting services using a SaaS safety database with integrated gateways to regulatory authorities.
Centralized weekly literature screening performed by qualified PV professionals to identify and assess safety signals and publications.
Development and maintenance of PSMFs, RMPs, PSURs, DSURs, PSSFs and other PV documentation to meet global and local regulatory requirements.
Gap analyses, development, implementation and maintenance of SOPs and Quality Management Systems aligned with GxP and ISO standards.
Expertise Areas
- Pharmacovigilance and drug safety operations
- Regulatory intelligence and compliance
- Global QPPV and local PV representation
- Safety database management and expedited regulatory reporting
Key Technologies
- Regulatory intelligence platform (country-specific reporting rules)
- SaaS pharmacovigilance safety case management databases
- Integrated regulatory reporting gateways/interfaces
- Centralized literature surveillance workflows
News & Updates
Participation in the ISoP Africa Chapter Meeting to discuss pharmacovigilance topics in Africa.
A discussion with Dr Helen Byomire Ndagij from the Uganda National Drug Authority about drug safety and pharmacovigilance.
An exploration of the roles and boundaries between LQPPV and NSC in pharmacovigilance.
Recognition event for excellence in the pharmaceutical industry.
Information about R3 ready reports for pharmacovigilance reporting.
Announcement of the release of the ikyzen platform for regulatory reporting.
Participation in the ISoP Africa Chapter Meeting to discuss pharmacovigilance topics in Africa.
A discussion with Dr Helen Byomire Ndagij from the Uganda National Drug Authority about drug safety and pharmacovigilance.
An exploration of the roles and boundaries between LQPPV and NSC in pharmacovigilance.
Recognition event for excellence in the pharmaceutical industry.
Information about R3 ready reports for pharmacovigilance reporting.
Announcement of the release of the ikyzen platform for regulatory reporting.