Biorepository and Laboratory Facilities

Advancing Clinical Research:
Biorepository and Laboratory Services

Biorepository and laboratory services are integral to the success of clinical research, enabling pharmaceutical and biotech companies to advance medical innovation through meticulous handling of biologic materials and precise laboratory processes. Whether it’s testing new molecules, conducting preclinical assessments, or analysing biological substrates such as bacterial strains, peripheral blood, or isolated cells, these services form the foundation of groundbreaking treatments and therapies.

At Camina Medical Experts, we are dedicated to providing comprehensive solutions that safeguard the integrity and availability of vital samples and ensure the reliability of laboratory operations. Our biorepository services adhere to strict environmental controls, including temperature and humidity regulation, to preserve the viability of biospecimens such as tissue, blood, plasma, and DNA. With secure infrastructure, meticulous data management, and full compliance with Good Clinical Practice (GCP) and GDPR standards, we offer tailored services that meet the unique demands of clinical trials, from long-term storage to complete sample inventory management.

Complementing these, our laboratory services focus on delivering high-quality support for clinical trials. From conducting over 75 laboratory audits to designing sampling kits, selecting and qualifying laboratories, and developing new testing methods, our expertise ensures investigators have access to precise, timely data that informs decision-making and upholds the integrity of trials. By combining technical precision with a commitment to patient-centred research, we empower teams to improve outcomes for those who rely on new treatments the most.

Together, our biorepository and laboratory services reflect Camina Medical Experts’ unwavering focus on supporting research with reliability, precision, and ethical integrity.

Camina Medical Experts is devoted to shaping the future of clinical research through its expertly crafted services. Our biorepository solutions are meticulously tailored to cater to the multifaceted demands of both clinical trials and preclinical research. By prioritising the preservation of sample integrity and facilitating seamless accessibility, our biorepository operations exemplify excellence, setting a benchmark in advancing medical science and innovation.

Some biorepositories focus solely on long-term storage, while others manage complete sample inventories for clinical trials—our services encompass both, ensuring flexibility and tailored solutions. We oversee the entire biospecimen collection process, from securing regulatory approvals to developing patient consent documents and collaborating with specialists who have access to the required patient populations. With their willingness to contribute to research, we ensure that valuable biological material is made available for studies that further medical progress. Our legal team stays updated on the latest documentation to ensure compliance with Good Clinical Practice (GCP) and the most recent GDPR requirements.

From collection to secure storage and processing, we provide the expertise and infrastructure to meet your biorepository needs—helping to advance research while prioritising patient welfare and ethical integrity every step of the way.

Biorepository facilities play a vital role in clinical and preclinical research, ensuring that biospecimens are preserved, managed, and made available for innovative therapies.

Our Expert-Led Features

• Environmental Regulation: Precise control of temperature and humidity to preserve the viability of biospecimens, including tissue, blood, plasma, and DNA.
• Flexible Storage Solutions: Customised options for long-term preservation and inventory management to align with specific study requirements.
• Secure Infrastructure: Robust facilities and systems to maintain biospecimen integrity and data security throughout the research lifecycle.
• Expert Collection Oversight: Expertise in regulatory approvals, patient consent processes, and collaboration with specialists to ensure seamless operations.
• Regulatory Compliance: Full adherence to Good Clinical Practice (GCP) and General Data Protection Regulation (GDPR) standards to uphold ethical and legal integrity.
• Patient Population Access: Strategic partnerships with specialists to secure valuable biological materials for impactful research studies.

Clinical laboratories play a pivotal role in the success of clinical trials, whether operating as local or central labs. Their accuracy and efficiency are critical to the study's progress, making the careful selection of partners indispensable. In oncological trials, or instance, investigators require prompt access to laboratory results to determine whether a patient is eligible to receive study medication. Reliable, timely data ensures patients receive the appropriate care while preserving the integrity of the trial.

Selecting the right laboratory involves far more than verifying certifications and accreditations. It demands a thorough evaluation of technical capabilities, regulatory compliance, and operational efficiency. At Camina Medical Experts, our laboratory specialists possess extensive experience, having conducted over 75 laboratory audits, ranging from system-level to study-specific assessments. We embed robust quality management systems, Good Clinical Practice (GCP), and Good Clinical Laboratory Practice (GCLP) standards, enabling research teams to collaborate with laboratory partners who uphold exceptional standards.

With a strong emphasis on oversight and expertise in laboratory assessments, we provide reliable, high-quality support for clinical trials, ensuring investigators have access to precise, timely data that informs decision-making and shapes research outcomes. Our experts bring a wealth of knowledge and practical experience essential for:

Key Offerings:

• Expert Auditing: Over 75 laboratory audits conducted, spanning system-level and study-specific evaluations.
• Custom Sampling Kits: Design and management of kits tailored to study-specific needs.
• Laboratory Qualification: Rigorous selection and validation to ensure compliance with GCP and Good Clinical Laboratory Practice (GCLP) standards.
• Efficient Supply Chain Management: Seamless logistics to ensure availability of sampling kits at trial sites.
• Innovative Laboratory Methods: Validation and development of methods to meet the unique requirements of clinical trials.

Camina’s laboratory services empower investigators with accurate and reliable data, driving progress in research and patient care."