Pharmacovigilance Translation
Rapid translation of adverse event reports and safety documentation. 24/7 support.
Time-Critical Drug Safety Translation
Our dedicated PV translation team provides 24/7 support to meet regulatory timelines for adverse event reporting.
From ICSRs to aggregate safety documents, we help maintain regulatory compliance across all markets.
PV Documents We Translate
Comprehensive PV translation support.
Adverse Event Reporting
- Individual Case Safety Reports (ICSRs)
- Serious Adverse Event (SAE) Reports
- Follow-up Reports
- Medical History Summaries
Aggregate Safety Reports
- PSURs
- DSURs
- PBRERs
- Risk Management Plans
Safety Communications
- Dear Healthcare Provider Letters
- DHPCs
- Medical Literature Translation
- Signal Detection Reports
Rapid Turnaround for Regulatory Compliance
Meeting critical PV reporting timelines.
Frequently Asked Questions
What is your ICSR turnaround time?
4-hour turnaround for urgent ICSRs. 24/7 availability including weekends.
Do you have MedDRA expertise?
Yes, our PV translators are trained in MedDRA coding and terminology.
Can you handle high-volume ICSR translation?
Yes, dedicated PV teams that scale for high-volume needs.
Do you translate spontaneous and solicited reports?
Yes, all types of adverse event reports from all sources.
Request a PV Translation Quote
Get a quote within 2 hours. Contact us for urgent support.
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Trusted by leading pharmaceutical and biotech companies
Need Urgent PV Translation Support?
Our 24/7 team is ready for your adverse event reporting needs.
24/7 availability - 4-hour ICSR turnaround - 150+ languages