ISO 21899 Biotechnology - Testing for Biological Material in Biobanks

EUROLAB, with its state-of-the-art accredited laboratories and expert team, provides precise and fast testing services within the scope of ISO 21899 testing. This standard specifies valid verification and validation requirements for a biobank to be able to demonstrate that it processes biological materials using validated or validated methods that are valid and fit for purpose.

ISO 21899 is designed for use in the application and validation of processing methods for biological materials.

The standard covers various aspects of biobanking, including the collection, processing, storage and distribution of biological samples and related data, and ethical and legal issues related to biobanking.

ISO 21899 provides guidance for the establishment and operation of biobanks, including the development of policies and procedures, risk management, quality control and staff training.

The standard highlights the importance of ensuring the privacy and confidentiality of donors and their personal information, as well as the need for informed consent for the collection and use of biological samples and related data.

ISO 21899 also covers technical requirements for biobanking, including the types of samples that can be collected, the conditions for their processing and storage, and methods for ensuring the integrity and traceability of samples and data.

Compliance with ISO 21899 is important to ensure that biobanks operate in a consistent and standardized manner and adhere to ethical and legal requirements for the collection, storage and use of biological samples and related data.

EUROLAB assists manufacturers with ISO 21899 test compliance. Our test experts, with professional working mission and principles, offer you the best service and controlled testing process in our laboratories to our manufacturers and suppliers.