Trial master file

A Clinical Trial Master File (TMF) is a collection of essential documents and records that allows for the comprehensive documentation and management of a clinical trial. It serves as the primary repository for all trial-related documents, providing a complete record of the trial’s conduct, data integrity and compliance with regulatory requirements.

Designing your trial master file with significant impact

Well-designed and informative materials not only facilitate participant understanding and engagement but also contribute to the overall integrity and credibility of the research. We are here to help. We offer several types of design and technical support. GSB Clinical’s graphic designers and pre-press personnel make both layouts and technical correction for clinical trial mater files and other documents verifying that the clinical trial has been conducted following regulatory requirements.

Your trusted printing partner of clinical trial materials

Typically, clinical trial printing will be printed on digital machines, due to low quantities of printing materials. However, offset services are available if required. All our printing machines and finishing equipment are state-of-the-art, and we can meet all customer product requirements in-house.

Shipping your clinical trial materials

Based on our in-house printing and warehouse facilities, we storage, pick and pack packages for shipping every day. We have a close cooperation with a carrier company specialized in pharma logistics with experience in worldwide distribution. They pick up current days shipping consignments every afternoon.

A partnership that gives you peace of mind

GSB Clinical is the only European printing company with vast experience within customized clinical trial solutions and specialized employees with thorough knowledge of medical terms under one roof. This unique combination enables us to run a seamless digital, graphic, printing and logistic workflow that ensures user-friendly clinical trial solutions for investigator staff and patients.

We work with Europe’s top pharma and biotech companies and have more than 25 years of experience in designing and producing products, services and logistics for clinical trials. Consequently, our team has a deep understanding of processes and workflows in the clinical trial printing, storage and logistics arena.

Equally important, we have a comprehensive and solid take on the services that pharma customers require of us to fulfill their individual demands in the printing and logistic process. We also ensure that our services, products and processes keep up with the ever-changing world and the requirements and needs from our customers.

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Sustainability and CSR

Working with sustainability and CSR allow organizations to contribute positively to the environment and society. By implementing a number of sustainable practices and engaging in CSR initiatives, GSB Clinical believe that the organization and the employees are making a meaningful difference within our line of business. Our focus is to avoid leaving a negative imprint on the areas where we do business.