ICM Administration CROs

2 contract research organizations in our directory list ICM Administration as a capability, across 2 countries. 1 reports GLP capability and 2 report AAALAC accreditation. Compare their species, services and accreditations below, and contact labs directly from their profiles.

2 CROs 1 GLP 2 AAALAC 2 countries

About ICM Administration

Intra-cisterna magna (ICM) administration delivers a test article into the CSF-filled cistern at the base of the skull. Compared with lumbar dosing it can give broader distribution to the brain surface and cerebellum, which has made it a common route for AAV and oligonucleotide programs.

Procedures range from a single percutaneous injection to an implanted catheter for repeat dosing and sampling. Technique, needle guidance and post-dose monitoring vary between labs, so experience with the specific species matters.

CNS drug delivery methods →

ICM Administration CROs

Showing 2 CROs. Order rotates daily so no lab is permanently listed first.

NeuroBridge

CN Verified GLP AAALAC

NeuroBridge Biotechnology is a specialized preclinical research organization based in Guangzhou, China, focused on non-human primate (NHP) and pig disease models and exploratory non-GLP translational studies. We support…

ICM Administration AAV Biodistribution Acute Toxicity ADME Studies Behavioral Assessment Cynomolgus monkey Minipig Non-human Primate Rhesus monkey

Biomere

US Verified AAALAC

Biomere (a JOINN company) is a preclinical CRO based in Worcester, MA. Services include non-GLP PK/PD, discovery toxicology, surgical services, disease models, and laboratory sciences. Surgical services include…

ICM Administration AAV Biodistribution Bioanalysis Bioavailability Studies Biodistribution Cynomolgus monkey Minipig Mouse Non-human Primate

Questions to ask when choosing a ICM Administration CRO

  • Is the procedure done percutaneously or via surgical exposure, and with what guidance?
  • What is your maximum validated dose volume for this route and species?
  • How do you monitor for and report procedure-related adverse effects?