Expert Support in Product Safety, Clinical Trial & Regulatory Solutions
Empowering Pharmaceutical, Biotech & MedTech organizations with integrated expertise in Drug & Device Vigilance, Clinical Research, Medical Writing, Regulatory Affairs, and Quality Systems.
Efficiency
Timely, cost-effective solutions without compromising quality
Partnership
Collaborative approach tailored to each client’s unique needs
Compliance
Timely, cost-effective solutions without compromising quality
Support
24/7 dedicated assistance throughout every stage of your project
We Are Vigiaris..
Excellence in innovation, compliance, and patient safety for the pharma and biotech industry.
Vigiaris is a specialized consulting partner offering scientific, regulatory, and safety expertise across the healthcare product lifecycle.
With a focus on innovation, compliance, and collaboration, we provide expert support across Pharmacovigilance, Clinical Trials, Regulatory Affairs, Medical Writing, QMS, and Device Vigilance.
Our Featured Services
We Provide All Exclusive
Services For Pharma and Biotech
Pharmacovigilance
We deliver accurate, timely, and compliant pharmacovigilance services to ensure patient safety and meet global regulatory requirements
Medical Device Vigilance
End-to-end device vigilance support including incident management, risk evaluation, trend analysis, and regulatory reporting in alignment with MDR and global standards
Clinical Trial Support
Expert documentation support to ensure clinical trials run smoothly and meet regulatory standards
Medical Writing
High quality scientific and regulatory writing tailored for submissions, publications, and communications
Regulatory Support
Comprehensive global submission services to accelerate approvals and maintain compliance across regions
Quality and Compliance
Robust systems, audits, and training to strengthen inspection readiness and regulatory compliance