Problem & Solution
Veterinary registration data is scattered across dozens of regulatory authorities worldwide, each using different formats, languages, naming conventions, and reporting standards. It is time-consuming to manually collect and validate data collection without a centralized source of truth, gaining a complete view of the global veterinary product landscape.
The Global Veterinary Registrations Database aggregates and harmonizes veterinary medicinal product registrations from major regulatory authorities worldwide into a single, continuously updated dataset. Through automated data collection, translation, standardization, and record matching, the platform provides a consistent view of veterinary pharmaceuticals and biologicals across global markets. Users can quickly identify where products are authorized, compare active ingredients, monitor authorization changes, analyze competitive landscapes, and support regulatory, commercial, and strategic decision-making with confidence.
Benefits & Use Cases
Competitive Intelligence
Monitor competitor product registrations, portfolio expansions, approvals, withdrawals, and geographic market presence.
Regulatory & Portfolio Strategy
Analyze registration status, active substances, authorization pathways, and market coverage across multiple countries.
Business Development & Licensing
Identify products, technologies, and companies with registrations in specific markets or therapeutic categories.
Market Intelligence & Opportunity Assessment
Evaluate therapeutic areas, product classes, active ingredients, and market saturation across regions.
Platform Preview
Data Coverage & Depth
Product Approvals
Coverage includes active ingredients, authorization status, MAH details, and Summary of Product Characteristics (SmPC).
Indications & Target Species
Detailed description of the animals, diseases, conditions, symptoms, or clinical outcomes for which the product is authorised.
Contraindications, Warnings & Adverse Reactions
Captures when the product should not be used, relevant safety considerations, potential side effects, and reported frequency categories such as common, uncommon, rare, or very rare.
Dosage & Administration
Includes precise dosing instructions, such as mg/kg body weight, administration intervals, maximum treatment periods, preparation instructions, and guidance by species or indication.
Withdrawal Periods
Records the required period between the final administration and the safe use of animal-derived products for human consumption. Products for non-food-producing species are identified as not applicable.
Storage, Shelf-Life & Disposal
Includes temperature ranges, protection from light or moisture, shelf-life after first opening or reconstitution, and instructions for the safe disposal of unused products or waste materials.
Interested in the Veterinary Product Registration Data?
Let’s discuss how our data & analytic tools can support your strategic goals.