Categories
Type at least 2 characters to search.
View all results →
BioIVT
About CRO
BioIVT combines biological specimen resources with contract research services for drug discovery and development.
Frequently Asked Questions
What services does BioIVT offer?
Services include in vitro ADME and DMPK studies, drug metabolism investigations, transporter studies and related consulting. Its HEPATOPAC research service is used for questions such as metabolic stability, metabolite identification and mechanistic hepatotoxicity. Separately, the company supplies human biospecimens and primary cells for research programs.
What should I include when requesting a proposal from BioIVT?
Describe the compound type, development stage and ADME or toxicity question. Distinguish a materials-only request from a study performed by the provider.
Where is BioIVT located?
Listed locations include Westbury, NY. Confirm the proposed delivery site when requesting a quote; capabilities may vary by facility.
How can I contact BioIVT through CROaccess?
Use the Contact CRO form or contact CROaccess with your project requirements. CROaccess offers free procurement support to help scope the work, coordinate provider discussions and compare proposals. Research and laboratory services are quoted separately.
Technology & Expertise
BioIVT combines biological specimen resources with contract research services for drug discovery and development. Its in vitro ADME portfolio addresses absorption, distribution, metabolism and excretion, including drug transporter and drug-interaction questions. Hepatic models are a particular part of its published research offering.
Core Services
Services include in vitro ADME and DMPK studies, drug metabolism investigations, transporter studies and related consulting. Its HEPATOPAC research service is used for questions such as metabolic stability, metabolite identification and mechanistic hepatotoxicity. Separately, the company supplies human biospecimens and primary cells for research programs.
Accreditations & Compliance
Confirm the applicable facility, quality system, study standard and required documentation with the provider when scoping regulated work.
