Meet us in India (Greater Noida, Delhi NCR) at CPHI on 26-28 Nov 2024 to Explore our Global Services

CLINICAL TRIAL PHARMACOVIGILANCE

Adverse Event Reporting: Systematic collection, assessment, and reporting of adverse events
Risk Management: Identifying, evaluating, and mitigating risks associated with clinical trials
Regulatory Compliance: Ensuring all activities comply with relevant regulatory guidelines and requirements
Safety Monitoring: Continuous monitoring and assessment of patient safety throughout the trial
Data Analysis: Analysing safety data to detect potential safety signals

POST AUTHORIZATION/ MARKETED PRODUCT PHARMACOVIGILANCE

Adverse Event Reporting: Collection, assessment, and reporting of adverse events from healthcare professionals and consumers
Risk Management Plans (RMPs): Development and implementation of strategies to identify, evaluate, and mitigate risks associated with marketed products
Periodic Safety Update Reports (PSURs): Regular reporting of safety data to regulatory authorities to maintain compliance
Signal Detection and Management: Continuous monitoring of safety data to detect and manage potential safety signals
Regulatory Compliance: Ensuring all pharmacovigilance activities comply with global regulatory requirements
Global Literature Monitoring: Weekly/Bi-weekly Literature Monitoring for potential adverse events
Medical Information Call Centre: Accepting call via Toll free number, Call Triaging and passing information to respective departments

GLOBAL PHARMACOVIGILANCE SERVICES