Research capabilities

From early proof of concept to registration-support studies.

A practical capability set across veterinary pharmaceuticals, animal health, field efficacy, safety, residues, vaccines, parasitology and study support.

Veterinary and animal-health research in practice

GLP / Laboratory Practice

Study types and evidence streams associated with laboratory-practice and registration programmes.

GLP

Residue Studies

Residue and metabolite studies in milk and meat, coordinated with analytical laboratories in New Zealand and overseas to support registration dossiers.

GLP

Bioequivalence

Pharmacokinetic comparison of formulations, bringing together study design, residue testing and analysis where required.

GLP

Target Animal Safety

Practical safety studies for veterinary products across production and companion animals, with welfare and ethical conduct built into delivery.

GLP

Animal Transfer Studies

Studies examining transfer of agrichemical residues through feed or soil into food of animal origin.

GLP

Efficacy Studies

Field efficacy work using access to production animals, farms and varied geographical locations throughout New Zealand.

GLP

Intramammary Studies

Study capability around dry-cow products, teat seals, milking-cow products and bovine mastitis research.

GLP

Vaccines

Pre-clinical and clinical vaccine studies including challenge, safety, efficacy and protective-effect work.

GLP

Endo- & Ectoparasiticides

Parasite-control studies including FECR, total-worm-burden work and access to suitable lice and tick study sites.

GCP / Clinical Practice

Clinical study delivery and investigator-led work in real animal and field environments.

GCP

Good Clinical Practice Studies

Clinical study delivery and management shaped by practical protocol adherence, traceable data and experienced investigator oversight.

Supporting Services

Practical services that help clients plan, monitor, document and advance a study programme.

Support

Pilot / Proof of Concept

Early-stage studies exploring efficacy, safety and feasibility before a larger registration programme.

Support

Study Monitoring

Independent or collaborative monitoring through site visits, data review, participant assessments and protocol-compliance checks.

Support

Marketing Studies

Practical studies that generate evidence required to support downstream product marketing and commercial use.

Support

Research Approval & Provisional Registration Support

Support preparing research-approval and provisional-registration documentation and planning the studies needed for a registration dossier.