Clinical Monitoring

We provide passionate strategic knowledge, specific guidance, and expertise for study execution across multiple therapeutic areas.

Expert Support for Your Investigators and Teams

Our experienced teams here at Siron Clinical bring their valuable knowledge and insight to clinical trials across a diverse range of therapeutic areas, including pediatric, oncology, and medical devices. They provide support that your teams can rely on.

Clinical Monitoring Services

Protocol, regulatory and ICH GCP compliance verification

Site identification

Feasibility visits

Site qualification and initiation

Regulatory document preparation and collection

Budget and contract negotiation

Site recruitment strategy

Site personnel training

Interim site monitoring

Initiation and management of CAPA

Accountability investigational material(s)

Study closure

Pharmacovigilance: assisting and ensuring appropriate reporting of CIOMS, DSURs, annual IDB updates

Services

Project Management

Flexibility, innovation, and integrity guide our approach to project management and leadership for the success of your clinical trials.

Clinical Monitoring

We provide passionate strategic knowledge, specific guidance, and expertise for study execution across multiple therapeutic areas.

Quality Assurance / Control

We pride ourselves on accuracy and integrity through a continual and dynamic process when it comes to quality assurance and quality control.

Regulatory Submissions

We manage the entire Regulatory Submission process carefully and efficiently, bringing the benefits of new treatments to patients sooner while maximizing research investments.

Get in Touch

We offer unparalleled knowledge, support, guidance, and extremely experienced clinical research professionals to the biotechnology, life science, and medical device industries.

Get in touch to learn more about how we can help navigate complex clinical trials in Europe.