Pharmacovigilance and Device Safety
Understand and Document the Specific Safety Requirements of Your Trial
The collection, assessment, and disbursement of safety information is an essential component of a clinical trial, and an integral part of Good Clinical Practice (GCP).
Alira Health works closely with clients to understand the specific safety requirements of each trial and understands the nuances and attention to detail needed—whether it relates to pharmacovigilance services for a drug trial, or device safety services for a device trial.
Why Choose Us for Pharmacovigilance and Device Safety Support?
As your partner, we will also implement a robust management system for project documentation, data collection, and generation of all required regulatory and periodic reports.
With Alira Health industry leading CRO as your partner, you will benefit from:
- Exceptional customer service and site relations
- In-depth expertise across the entire clinical trial process
- Flexible and tailored service delivered by multidisciplinary and global teams
- Frequent, transparent, and professional communication
- Guarantee we will lead your study efficiently, safely, and successfully
