Therapeutic Expertise
Perioperative
Our perioperative team runs trials in the surgical setting — anaesthesia, post-operative pain and recovery — where timing, standardisation and safety monitoring are critical.
Perioperative research requires tight coordination with surgical and anaesthetic workflows and careful, time-sensitive endpoint capture. Our physician-led team designs protocols that integrate with theatre schedules while maintaining rigorous safety monitoring and reliable outcome measurement.
Addressing common pain points in perioperative clinical trials
Time-critical assessments around surgery
Perioperative endpoints must be captured at precise time points around the procedure.
We design assessment schedules that fit real surgical and recovery workflows to protect data quality.
Standardising analgesic and anaesthetic endpoints
Pain and recovery outcomes are sensitive to concomitant medication and protocol variation.
We standardise rescue-medication rules and validated pain scales across sites.
Safety monitoring in acute settings
The perioperative period carries elevated, time-concentrated safety risk.
Our medical monitoring provides close, real-time oversight through the acute window.
Resources
Perioperative clinical trial resources
Improving Post-Operative Pain Clinical Trials
Design considerations for post-operative pain studies.
Evidence & insights
Perioperative white papers
Open-access reports from our physicians and data science teams — free, no sign-in.
The iNGENū CRO difference
Australian expertise, direct FDA submission
We uniquely combine Australian expertise with direct FDA submission capabilities, offering a streamlined path for sponsors to achieve global approval. Trial data from Australia can be submitted directly to the FDA via our E-Gateway, eliminating the need for third-party intermediaries.
iNGENū takes a highly strategic and disciplined approach to clinical research, ensuring every dollar is directed toward generating meaningful outcomes — eliminating unnecessary costs while maintaining the highest scientific and regulatory standards across the Asia-Pacific region.
“We have been using iNGENū for a Phase 1, first-in-human trial of our investigational drug — medical writing, project management, clinical data management and full end-to-end execution and monitoring. We have been particularly impressed by the out-of-the-box creative solutions to speed up and reduce overheads during this clinical trial.”
Giles MossChief Executive Officer
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