Quality is our foundation

At Vetspin, quality drives every decision. All studies follow Good Laboratory Practice (GLP) and Good Clinical Practice (GCP) guidelines to ensure integrity, traceability, and regulatory.

    • Standard Operating Procedures (SOPs) for all activities
    • Validated analytical methods
    • Full sample and data traceability
    • Internal/external audits
    • Secure data management and archiving
    • Ongoing process improvement
    • Continuous staff training and qualification

Clients can rely on reproducible, defensible, and regulatory-ready results, the foundation of long-term trust.

Quality assurance

Full GLP/GCP compliance and documentation integrity.

Vetspin operates with highly qualified personnel (graduated in Veterinary Medicine, Pharmaceutical Sciences and Technology and Veterinary Biotechnology) who undergo continuous training within the company or at accredited organizations. The aim is a constant collaboration and improvement to assure updated methods and techniques depending on study requirements.

The presence of a Quality Assurance program, consisting of study-, facility- and procedure-based audit, ensures the internal control of the GLP and GCP requirements; moreover a system of procedures allows managing all the critical and salient points for the performance of the studies. Quality Assurance has also the task of preparing the test facility to the biennial GLP regulatory authority inspection.

GLP

Vetspin is certified for the Good Laboratory Practice since 2006. The studies performed under GLP are as follows: 

    • Residue studies 
    • Pharmacokinetics/Toxicocinetic/ADME studies (also bioavailability and bioequivalence studies)
    • Physical-chemical testing

 

The Quality Assurance guarantees the maintenance of a quality program, consisting of study-, facility- and process-based audit which ensures the internal control of the GLP requirements; moreover a system of procedures allows managing all the critical and salient points for the performance of the studies and the management of the processes at the facility. The Quality Assurance has also the tasks of preparing the test facility to the biennial GLP regulatory authority inspection and of training personnel for GLP.

Vetspin is registered at Italian Ministry of Health as CRO for Good Clinical Practice since 2013.

GCP

The studies performed under GCP are

  • Clinical trial
  • Dose confirmation studies
  • Efficacy studies

There is a system of procedures to organize the various stages of the study and the processes of the facility. The Quality Assurance Unit performs audits to the study, both on documents and on the experimental phases. Quality control of data is part of the quality assurance and has the duty to verify the correctness of the data processing and the input of the data in the study.

Biostatistics & Data Management – Protocol design, validation and statistical reporting.

Documents needed for the conduct of the experiment and study milestones are produced in agreement with regulatory standards and archived at the end of the study in appropriate conditions of storage and confidentiality.
Experts of clinics, statistics, chemistry, and histopathology support Vetspin activities with particular reference to study planning and conduct.