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Regulatory Access to Biospecimens in the European Union: Procurement, Collection & Compliance for Research

2026-04-14T15:33:47+01:0018/03/2026|

Access to human biospecimens for EU preclinical research is governed by regulatory frameworks protecting donors, data, and ethics. Read the complete blog at BioIVT's website.

New Approach Methodologies (NAMs) in Preclinical Research: Redefining Toxicology Without Animal Models

2026-04-14T15:16:18+01:0002/03/2026|

Preclinical safety assessment has traditionally relied on animal studies to identify potential toxicities and guide first‑in‑human dosing decisions. Read the full blog at BioIVT.

Logistics and Cold Chain Challenges in Rapid Delivery of Human Biospecimens for Preclinical Research

2026-03-18T13:23:20+01:0012/02/2026|

Human biospecimens are essential for preclinical research, but their value goes beyond their biological origin. Sample handling, storage, and transport impacts on their quality and, therefore, on the reliability [...]

Quality‑Assured Human Biospecimens: From Collection to Preclinical Use

2026-02-12T06:44:19+01:0021/01/2026|

Human biospecimens are a critical input for preclinical research, but their scientific value is highly dependent on how they are handled throughout their lifecycle. Variability introduced during collection, processing, [...]

Cryopreserved primary human liver cells: improving reproducibility and scalability in preclinical assays

2026-01-14T17:55:56+01:0018/12/2025|

Cryopreserved primary human liver cells offer a practical balance between biological relevance and operational efficiency. When handled correctly, cryopreserved hepatocytes and non-parenchymal cells (NPCs) retain key metabolic, transporter, and [...]

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