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Better understanding and accurate assessment of both the country and the site levels are key to trial success. With detailed feasibility data at hand and reliable predictions of enrollment rates, efficient planning of trial milestones and choosing the right sites becomes more realistic. Clinbit’s dedicated and experienced team works closely with you offering an integrated approach. Your success is the result of our knowledge, experience, and commitment.
We prepare and check the required documentation for the completeness and correctness. We have extensive experience in negotiating contracts and budgets based on the specific requirements of a given country and center, shortening the contracting time to the necessary minimum. We complete the documents and prepare the sites for activation.
We complete the documents necessary to submit applications and obtain positive opinions and approvals from registration authorities on time. We adapt patient materials to local requirements in the European Union and in Poland. We ensure effective communication between sponsor and registration authorities and timely delivery of required reports.
Recruiting participants in a clinical trial is a key issue in its implementation. Choosing the right recruitment tools based on a detailed "Enrollment Plan", such as recruitment announcements, materials for patients, creating a network of cooperating centers or contacting patient associations is often a necessary element of the study. We have already successfully supported many studies and dozens of sites.
Clinbit monitors are knowledgeable, well-trained, highly effective and very experienced – averaging more than 10 years of monitoring experience. They are partners for both investigators and sponsors, supporting study sites and guiding site personnel. Our goal is to ensure compliance with ICH-GCP Guidelines, local regulations, SOPs, and the study protocol. We are focusing on the real needs to keep study running efficiently, ensuring the collection of accurate and reliable data.
by choosing Clinbit you ensure clinical trials management by highly qualified project managers overseeing the project and responsible for its completion on time and on budget. Our project leads have experience of leading clinical trials in different therapeutic areas, study phases and types. They are the real team leaders creating great teams and amazing culture of work, focused on the customer, quality, and deliverables.
Live or online training where participants will learn the most important guidelines and fundamental principles used in scientific research. This course provides an overview of the various areas of GCP and application examples for conducting and monitoring clinical trials.

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