We understand each medical innovation is unique, so we tailor our services to meet the specific needs of your clinical trial.
Explore our areas of expertise, ranging from clinical operation, medical affairs, data management, and pharmacovigilance to local sponsorship for international companies.
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.
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.
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.
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.
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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