Simple, streamlined human tissue samples pattern procurement—it’s viable with iBioSpecimen. Whether you want completely consented FFPE blocks with unique version profiles, archived samples, or prospectively-accrued diseased tissue over the years with matched quad sets, we’ll cope with the procurement of gymnastics to get your biospecimens delivered. Because we’ve got get right of entry to the overall digital clinical record.
We are able to choose and annotate specimens with molecular and genetic characterizations, remedy data, results data, and different pertinent affected person and specimen data. Let us realize the unique tissue samples you want and we’ll faucet into our international community of biospecimen providers.
iBioSpecimen Marketplace is a fast, compliant, revolutionary one-stop access to millions of human biofluids and patients from a diverse network of providers
We have a vast and expanding network of partners, enabling us to access a wide array of Ibiospecimens with highly specific characteristics for various disease indications. If you need it, we can likely obtain it. Here are some examples of disease human tissue samples.
If you need it, chances are, we can get it. Our large and growing network of partners connect their electronic medical record data directly to the iBioSpecimen Marketplace, allowing us to source Ibiospecimens for research with highly specific characteristics for a broad range of human tissue samples. Below are some examples.
By partnering with iBioSpecimen, you gain extensive access to richly annotated human biospecimens and patient encounters. This is made possible by our growing network of partners, including hospitals, biorepositories, commercial laboratories, HIEs, and other healthcare organizations around the world. Available best human tissue samples
“This process previously required a lot of paperwork and time. iBioSpecimen makes it so much easier and quicker.”LeeAnn Talarico
Human tissue samples are small pieces of biological material, such as cells, organs, or fluids, taken from the human body for medical or research purposes.
Human Tissue samples are collected for various reasons, including diagnosing diseases, conducting medical research, developing treatments, and monitoring treatment effectiveness.
Tissue samples can be collected through surgical procedures, biopsies, blood draws, and various non-invasive methods like swabs or urine samples, depending on the type of tissue needed.
Yes, there are ethical guidelines and regulations governing the collection of human tissue samples. These guidelines emphasize informed consent, privacy, and ensuring that the samples are used for legitimate medical or research purposes.
Informed consent is a process where individuals are fully informed about the purpose, risks, and benefits of collecting their tissue samples, and they voluntarily agree to participate in the collection.
Tissue samples are used for studying diseases, developing new treatments, understanding genetic factors, and investigating cellular and molecular processes in the human body.
Tissue samples are typically stored at low temperatures, often in specialized freezers or cryopreservation facilities, to maintain their integrity for future research or diagnostic purposes.
Biobanks are institutions that store and manage large collections of human tissue samples and associated data. They play a crucial role in advancing medical research and personalized medicine.
Yes, with appropriate ethical approvals and data privacy safeguards, tissue samples can be shared among researchers and institutions to promote collaborative research.
Challenges include obtaining sufficient and representative samples, ensuring sample quality, addressing ethical and consent issues, and managing data associated with the samples.
Yes, there are concerns about the potential for re-identification of individuals from genomic data and the need to protect the privacy of donors, which is addressed through data anonymization and strict access controls.
Regulations vary by country, but they often include laws related to informed consent, patient rights, data protection, and ethical review processes.