Preclinical & Translational DevelopmentPreclinical Development & IND-Enabling
IND-Enabling Programs & Preclinical Management
Compare vendors for ind-enabling programs & preclinical management within Preclinical Development & IND-Enabling, covering IND-Enabling Study Programs, Preclinical Program Management & CRO Oversight.
Capabilities in this workflow
Vendors supporting this workflow
CRO / Research Services Provider · +3 more types
Altasciences is an early phase CRO and CDMO providing toxicology, IND-enabling studies, clinical pharmacology, bioanalysis, and drug manufacturing.
Products: Acceleration Platform
Evidence-backed workflow match
“Based on a custom-designed research program, we will conduct individualized nonclinical studies to ensure that your IND/NDA-enabling toxicology, safety pharmacology, and…”Source: altasciences.com
Also offers: Toxicology Studies, First-in-Human (Phase I) Clinical Pharmacology Support, +1 more
CRO / Research Services Provider · +5 more types
Inotiv is a CRO and research models provider offering toxicology, in vivo pharmacology, research and transgenic models, bioanalysis and DMPK.
Products: Teklad, Target Sufficiency +1 more
Evidence-backed workflow match
“Inotiv’s comprehensive IND support services, designed by scientific and regulatory experts, streamline the IND process for efficient regulatory approval of your new therapy.”Source: inotiv.com
Also offers: Toxicology Studies, In Vivo Pharmacology & Efficacy Models, +3 more
CRO / Research Services Provider · +5 more types
Frontage Laboratories is a CRO and CDMO providing bioanalysis, DMPK and ADME studies, toxicology, Phase I support, and drug manufacturing.
Evidence-backed workflow match
“Our fully-integrated IND-enabling programs include general toxicology plus genetic toxicology and safety pharmacology as appropriate, plus all affiliated analytical /…”Source: frontagelab.com
Also offers: Bioanalysis & Biomarker Assay Services, Integrated CDMO/CMO Services, +3 more
Service Provider · +2 more types
ProductLife Group is a life sciences consulting and outsourcing group for regulatory affairs, pharmacovigilance, quality and validation, and market access.
Products: D.AI.M.I.
Evidence-backed workflow match
“IND-enabling study design and GLP oversight”Source: plglifesciences.com
Also offers: Regulatory Development Strategy & Agency Interactions, End-to-End Pharmacovigilance Outsourcing, +6 more