About Pleiad

Pleiad is a specialist clinical research organization. We provide regulatory and clinical trial management services to medical device, diagnostics, and ophthalmology companies. Quality is at the heart of all that we do.

We are a certified woman owned business.

We offer a very flexible approach: full service support or individual services as required. In the early stages of a project we develop the regulatory strategy, assist in negotiations with regulators, and design any clinical studies that may be required. Pleiad sets up and manages clinical trials and supports clients through the process of obtaining regulatory approval, preparing, submitting, and managing all regulatory documentation.

We operate in the USA and Europe with our own staff. We can manage projects in other territories using Pleiad-qualified partners.

For full service projects we appoint a Project Leader. Pleiad Project Leaders are senior, experienced, mature individuals who are responsible for the quality and timeliness of all deliverables and milestones. They are the client advocate within Pleiad and the main liaison with the customer. All members of the project team report to the Project Leader.

Pleiad's SOPs accommodate medical device, diagnostics, and pharmaceutical trials, and all our staff members are trained on US and EU medical device, diagnostics, and pharmaceutical product regulations.

The Pleiad name and logo are trademarked.