Aqlivia is a global specialty CRO headquartered in Netherlands- India and Middle East, dedicated to serve its clients as a true partner in Pharma drug development, clinical trial.  Aqlivia directly covers more than 20 countries and all key markets in Asia-Pacific, Japan, Europe and N. America, South Korea.
As a premium CRO and being recognized as the quality leader, we focus on the Major therapeutic areas Globally.
Aqlivia provides pre-approval and post-market pharmacovigilance (PV) expertise for pharmaceutical drugs (brand and generic), biologics, radiopharmaceutical drugs, natural health products, medical devices and cosmetics.  Our experienced staff deliver Clinical Research and PV services at all levels including specialist, strategic, and safety physician services.
 
Team is led by Dr Martin, Dr Victor and Mr Jami KK. Complete team bring over 15+ years of combined European, Australian global experience in R&D and medical information and are recognized as expert auditors, trainers and presenters.  

Our professionals can lead or support your Contract Research activities with the required rigor.  Our consulting services include:

•	Pharmacovigilance Self-inspections and Gap Analyses
•	GVP Inspection Preparation and Assistance
•	Pharmacovigilance Training Customized to Meet Your Needs
•	Pharmacovigilance Agreements 
•	Pharmacovigilance Standard Operating Procedures
•	Safety Physician Services 
•	Foreign Marketing Authorisation Holder and/or Importer GVP Services
•	Benefit–Risk Assessments
•	Risk Management Plans
•	Aggregate Reports
•	Individual Case Safety Report Processing
•      Literature (worldwide and local)
•      Medical Information (call centre services)

AQLIVIA GLOBAL RESEARCH

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AQLIVIA GLOBAL RESEARCH

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Teams

Offices

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