Veterinary Pharmacovigilance Services

At OC Vigilance, we provide specialized veterinary pharmacovigilance services to ensure the safety and efficacy of medicinal products used in animals. Our approach focuses on detecting, evaluating, studying, and preventing adverse effects or any other issues related to the use of veterinary medications, adhering to both national and international regulations.

OC Vigilance offers the pharmaceutical industry the following services to carry out the tasks stipulated in current legislation

Our services include
  • Pharmacovigilance System Implementation and Preparation of Standard Operating Procedures and the Pharmacovigilance System Master File
    We assist in the implementation of pharmacovigilance systems for clients who do not already have one, as well as in drafting various standard operating procedures (SOPs) and the pharmacovigilance system master file (PSMF). We also support the updating and/or review of these documents.
  • Acting as Qualified Person for Pharmacovigilance (QPPV)
    We offer a comprehensive service, acting as the pharmacovigilance Responsible Person at both the European and Spanish levels, and/or as a deputy. We ensure appropriate pharmacovigilance training and effective performance of activities overseen by the pharmacovigilance Responsible Person.
  • Management of Suspected Adverse Events in Animals
    We monitor and manage reports of suspected adverse events related to the use of veterinary medicinal products, providing timely and accurate responses to minimize risks and improve animal and/or human health.
  • Pharmacovigilance Bibliographic Search Service
    We provide a specialized service in pharmacovigilance bibliographic searches, where we conduct a thorough and systematic investigation of the relevant scientific literature. Our focus is on identifying and collecting critical drug safety information, ensuring that our clients have accurate and up-to-date data for decision making. We use recognized databases, both globally and locally, and apply rigorous criteria to ensure the quality and relevance of the results, thus facilitating a thorough and effective analysis of the available information.
  • Post-Marketing Safety Monitoring
    We provide continuous monitoring of veterinary medications after their market release, offering support in the planning and preparation of signal detection reports.
  • Pharmacovigilance Audits
    We conduct comprehensive audits of veterinary pharmacovigilance systems to ensure compliance with national and international standards, providing strategic recommendations for process improvement.
  • Veterinary Pharmacovigilance Consulting
    We provide personalized veterinary pharmacovigilance consulting services, helping our clients resolve any questions or challenges that may arise in their pharmacovigilance activities. Our approach is tailored to their resources and specific needs, ensuring full compliance with current regulations.
  • Medical Advisory Services
    We have qualified veterinarians in our team to support our clients in any pharmacovigilance activity and/or medical inquiries.
  • Post-Authorization Studies
    We offer full support in the pharmacovigilance management for post-authorization safety studies (PASS), ensuring regulatory compliance and ongoing treatment safety. Our team handles the collection, analysis, and reporting of safety data, helping identify risks and trends in the long-term use of medicinal products in real-world settings.
  • Veterinary Pharmacovigilance Training
    We provide ongoing training for internal teams on veterinary pharmacovigilance good practices, ensuring alignment with industry standards.
  • Communication with Health Authorities and Application Use in Pharmacovigilance Activities
    We assist in setting up various applications for the necessary communications with health authorities and provide support for their use (EVVET, IRIS, etc.).