Pharmacovigilance
- Capabilities
- Services
- Why us?
Pharmacovigilance:
 
bullet Capabilities:
 
bullet EU Qualified Person Services
bullet Risk Management Statements
bullet Drug Safety Database Management
bullet Serious Adverse Event Processing
bullet Huge pool of experience with studies aimed at submission to different agencies
bullet 24/7 Medical and Safety Cover
bullet SAE/ADR: Receipt and Triage, Data-Entry, Narrative Writing, Medical Review including Label Assessment, Causality Statement, Quality Control, Submission to Health Authorities
bullet ICSR Handling
bullet Literature search
bullet PSUR generation
bullet Signal detection and evaluation
 
bullet Services:
 
bullet EU Qualified Person Services
bullet Risk Management Statements
bullet Safety Database Management
bullet Adverse Event Processing
bullet Literature search
bullet PSUR generation
bullet Signal detection and evaluation
 
bullet Why us?
 
bullet Multilocational : UK, Poland and India
bullet Partnership with Large and Small Clients
bullet Small Clients: Can perform end to end pharmacovigilance activities including safety database services
bullet Large Clients: Can Operate using Client's database leading to decreased resource expenses
bullet Trained and Experienced Staff
 

Lambda Therapeutic Research Ltd.
A CRO for Clinical Research, Clinical Trials, Medical Writing, Bioanalytical, Bioequivalence and Pharmacovigilance services.
India (Ahmedabad - Mumbai), Poland (Warsaw), USA