Medical Affairs

Patient safety and scientific integrity are our highest priorities. Our Medical Affairs team ensures each study is governed rigorously, and reporting guidelines are met to the standard mandated by regulatory authorities.

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.

Medical Monitoring

Our Medical Monitors are medical practitioners with  extensive industry experience, so you can rest assured that any serious adverse event in your trial will be identified swiftly, and handled in accordance with relevant laws, as well as  the ICH-GCP guidelines.

Strategic Consulting

Our team of experts will work seamlessly as part of your team to help you make informed decisions  from study design through to competitive landscape analysis so  your trial is appropriately designed and well managed.

Medical Writer

Our Medical Writers have expert capabilities to assist with all aspects of clinical trials from protocol writing to Clinical Study Report (CSR) development across a broad range of therapeutic areas and all phase of clinical trials.

Medical Information

Our Medical Information Team will gather, analyse and communicate medical queries to the internal and external stakeholders involved in running of your clinical trials. We will ensure that the information regarding your product is accurate, compliant and up to date.  

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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