Drug Safety and Pharmacovigilance:
 
ICBio is dedicated to provide a strategic team to clients meeting their expectations and beyond. The team can effectively provide active management of drug safety, risk management and patient health during the entire lifecycle of a product from preclinical through the conclusion of the marketing period of a product.

The services include right from helping setting up a data base, managing the adverse events, Global safety reporting, regulatory reporting, Coding through Globa dictionaries like MeDRa, strategic planning for trend analysis and risk management.
 
 
Services of ICBio under Drug safety and Pharmacovigilance include:
 
World class services in terms of delivering Quality data
Short lead-in times, clear and concise processes tailor made to meet client expectations ultimately leading to effective client management and their satisfaction
Provide our support across all global time zones (24/7 services)
Deliver services within time and budget, further assist in lowering the overall cost base for drug safety activities that is ensured through focus on
 
>> Re-allocation of resources
>> Lower recruitment and headcount expenses
Focus on Strong QA and QC sticking to compliance and leading to
 
>> Reduction in business risk to due favorable inspection outcomes
>> Faster time to market
 
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