Our Services

Jupiter Global Bio-Research offers comprehensive site management solutions to support the efficient conduct of clinical trials. Our services include:

• Site Feasibilities: Assessing the suitability of potential clinical trial sites based on various factors, including geographical location, infrastructure, and investigator expertise.
• Site Development: Providing support for the development and preparation of clinical trial sites, including obtaining necessary approvals and ensuring compliance with regulatory requirements.
• Site Selection: Identifying and selecting the most appropriate clinical trial sites based on study objectives and feasibility assessments.
• Site Coordination: Managing and coordinating activities at clinical trial sites, including investigator training, patient recruitment, and data collection.

Study Start-Up Activities

In addition to site management, we also provide essential study start-up activities to ensure a smooth and timely initiation of clinical trials. These services include:

• Regulatory Submissions: Assisting with the preparation and submission of regulatory documents to obtain necessary approvals.
• Investigator Training: Providing training and education to investigators and site staff on study protocols, procedures, and regulatory requirements.
• Informed Consent Development: Developing and obtaining informed consent documents from study participants.
• Patient Recruitment Strategies: Implementing effective patient recruitment strategies to enroll eligible participants.
• Site Initiation Visits: Conducting initial site visits to assess readiness and ensure compliance with study protocols.

By providing comprehensive site management and study start-up services, Jupiter Global Bio-Research helps clients streamline the clinical trial process and achieve their research objectives.