Biosamples

A healthcare worker in blue scrubs and mask assists a woman donating blood in a clinic, using a device to monitor her vitals.

Comprehensive services for
clinical sample collection
and for IVDR certification

Pratia provides comprehensive biosample collection services for clinical trials and IVDR studies, combining speed, quality, and compliance. Our international network of Research Sites and hospital partnerships enables access to diverse patient populations across multiple therapeutic areas.

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For biobanks

Pratia supports biobanks with prospective biological sample collection across diverse patient populations and therapeutic areas. Through our international network of interconnected Research Sites and embedded hospital collaborations, we enable efficient access to large patient cohorts within short timelines. Our experienced Study Teams manage the full operational pathway, including sample collection, temporary storage, processing coordination, and transportation of biomaterial in compliance with ethical, regulatory, and protocol requirements. By combining strong site-level execution with standardized processes and centralized oversight, Pratia ensures reliable, high-quality biosample delivery aligned with study objectives.

A person wearing blue gloves examines petri dishes in a lab, with stacks of dishes in the foreground and background.

For ivd manufacturers

Pratia supports IVD manufacturers with biosample collection programs designed to meet requirements under Regulation (EU) 2017/746 (IVDR). With our detailed knowledge of the legislative framework we assist the manufacturers of in vitro diagnostics to meet the IVDR requirements. Our know-how also includes the preparation of all documentation for IVDR, including clinical evaluations and the Performance Evaluation Plan (PEP).

Services

Data management

We provide statistical analysis of clinical data, preparation of Case Report Forms (CRFs), and monitoring in collaboration with local partners.

IVDR documentation

We prepare the documentation package in accordance with the European Parliament and Council Regulation (EU) No. 2017/746 (IVDR) and arrange its submission to the ethics committee and the relevant regulatory authorities.

Sample collection

Thanks to our vast network, we can obtain a significant quantity of various types of clinical samples quickly.

Validation of CE IVD Kits

We verify the performance evaluation of IVD kits in accordance with requirements of IVDR regulation.

Analysis of samples

We verify the quality and parameters of collected samples, analyze their physiological and biochemical properties, we control the sample labeling, and assess other necessary characteristics

Recruitment campaigns

We run integrated campaigns using both digital and traditional media. Our multichannel patient outreach includes SEO/SEM, targeted social media, educational websites, as well as offline channels like print, radio, and outdoor ads.

Storage of samples

We offer temporary storage of biological samples in Ultra Low Temperature Freezers with 24/7 temperature monitoring (-80 °C).

Shipment of biomaterial

We can arrange a safe and controlled shipment of biological samples between collection centers, laboratories, and biobanks in cooperation with specialized shipment services.

Why choose Pratia for biosample collection?

Pratia delivers biosample programs through a structured international Research Site Network designed for speed, quality, and compliance.

Our network spans more than 100 interconnected Research Sites across Europe, the US and Turkey, enabling rapid identification and enrollment of eligible patients across multiple indications.

We offer an integrated site execution model. Pratia's dedicated sites, embedded hospital units, and hybrid operational models allow us to select the optimal collection strategy for each biosample program.

Our Investigators, Study Coordinators, and Study Nurses manage biosample collection according to protocol requirements and international quality standards.

We coordinate multicenter biosample collection aligned with sponsor documentation strategies and regulatory expectations under IVDR.

Through multichannel patient recruitment campaigns, we help accelerate identification of eligible participants when required.

We have a good knowledge of local legislation, requirements for the validation of CE IVD kits and the collection of biological samples.

Research Sites operate validated temperature-controlled environments and standardized procedures supporting reliable biomaterial handling

We cooperate with established laboratory partners supporting analysis workflows linked to diagnostic validation and clinical trials.

Pratia operates within structured quality systems aligned with international clinical research standards and continuous process improvement practices.

Collected biological samples are stored in Ultra Low Temperature Freezers with continuous temperature monitoring at -80 °C. Our Lab Freezers are operated by trained staff 24 hours a day, seven days a week.

We are a member of SCRS (Society for Clinical Research Sites) and frequently (actively) participate in international congresses oriented to research and development in field of biomedicine. We are constantly improving our processes.

Our experienced Study Teams manage the full operational pathway, ensuring reliable, protocol-aligned biosample handling.

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Case study: Multicenter respiratory infection biosample collection

Pratia supported a multicenter biosample collection program for respiratory infection diagnostics involving approximately 1,000 symptomatic patients. Study Teams coordinated patient enrollment, protocol-aligned swab collection, and temperature-controlled temporary storage across participating Research Sites, ensuring compliance with sponsor specifications and regulatory requirements. Collaborating with certified laboratory partners across Europe, Pratia enables biosample programs for diagnostic development, biomarker research, and clinical trials.

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Start your biosample collection program with Pratia

Our teams are ready to support your project, from patient identification to secure sample handling. Partner with Pratia for efficient, compliant, and high-quality biosample acquisition.

Ready to start your clinical trial?

Discover how our flexible approach can support your unique study needs.