Clinical Operation

We understand each medical innovation is unique,  so we tailor our services to meet the specific needs of your clinical trial.

We provide end-to-end solutions for all phases of clinical trials.

Explore our areas of expertise, ranging from clinical operation, medical affairs, data management, and pharmacovigilance to local sponsorship for international companies.

Strategic Consulting

Together with our in-house experts and renowned Key Opinion Leaders (KOLs), we will provide strategic solutions on planning and execution of your clinical trial to maximize your product’s potential.  

Project Management

Your trial will be well managed from start to  finish with our fully qualified resourcing.
We will assign a dedicated Project Manager  to your study to ensure your trial  is conducted on time, within budget and to a high standards.

Trial Monitoring

Our Clinical Research Associates (CRAs) combine high-caliber qualifications with excellent interpersonal skills to build and maintain effective relationships with the site staff throughout the life cycle of the study.

Trial Documentation

Our team of experts will develop study specific documents and manage Human Research Ethics Committee (HREC) submission packages, so your trial is approved in a timely manner.

You’ll be working with highly skilled professionals

Complete Phase CRO is dedicated to helping small to medium size biotechnology and pharmaceutical companies worldwide advancing their innovative products and breakthrough science in to new medical treatment.

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