Safety and
Pharmacovigilance

Complete range of in-house services

Clinical trials safety monitoring and reporting is vital to ensure participant safety, data integrity and regulatory compliance. Regulatory guidelines around clinical trial safety monitoring and reporting demand strict safety management procedures, from a highly-skilled, and experienced safety team.

get in touch with our
clinical operations team

Delivering more than 30 years experience of drug development expertise

Technology

Avance Clinical’s state-of-the-art built-for-purpose technology facilitates the management, reporting, and analysis of key safety information that may arise during study conduct.

Our safety monitoring and reporting services ensure regulatory compliance, and monitoring of the study drug safety profile to identify, evaluate and minimize safety-related risks at a reasonable cost.

Deep Regulatory Knowledge

Avance Clinical’s clients benefit from deep regulatory knowledge, a state-of-the-art safety and pharmacovigilance electronic database Argus, and a multi-disciplinary safety team with diverse therapeutic area expertise and decades of experience in safety management and reporting.

WHY BIOTECHS CHOOSE
AVANCE CLINICAL

More than three decades of deep clinical research management experience, Avance Clinical is the largest
specialist Australian and US CRO delivering quality clinical trials in Australia, New Zealand, Asia and North America for international biotechs.

43.5%

REBATE

5-6 Wks

START-UP TIME

100%

CAPABILITIES

FDA

COMPLIANT RESEARCH