Véto-pharma is not only a major player in bee health, but also a key player in animal health!
Indeed, the Véto-pharma Manufacturing department offers bespoke manufacturing services. As a CDMO (Contract Development Manufacturing Organisation), we support our clients in the success of their projects with excellence, through a customer service that is local, agile, and efficient.
Our quality indicators, customer satisfaction, and loyalty are a testament to our ability to meet the demands of the animal health sector.
Our production site in Chaillac, France
Located in Chaillac in France, since 1988, our industrial site covers 10,000 m² and includes 3 production workshops, designed to meet the highest pharmaceutical quality standards.
Equipped with facilities compliant with Good Manufacturing Practices (GMP), our workshops are fully dedicated to the production and packaging of non-sterile veterinary products for external or oral use.
We manage our resources with agility and responsibility, prioritizing strategic investments that ensure a sustainable and beneficial impact for all.
Our CDMO services
Contract manufacturing and packaging services: bulk, primary, and secondary
3 manufacturing workshops across different production and packaging lines:
- Liquid: emulsion, solution, suspension, etc.
- Semi-liquid: gel, paste, cream, ointment, etc.
- Extrusion of medicinal polymers
With great flexibility in batch sizes and a wide range of packaging options, both large and small.
Formulation developement and industrial transfer
We specialise in the development of medicines (excluding injectables, cytotoxic drugs, and ß-lactams), hygiene and care products, as well as food supplements.
Our formulations cover various pharmaceutical forms, including liquids (emulsions, solutions, suspensions…), semi-liquids (gels, pastes, creams, ointments…), and extruded forms, including drug polymers and collars.
Analytic development
Our dedicated team offers a bespoke analytical development service:
- Adaptation of an existing method in the case of a reformulated product (change in form, excipients, or industrial manufacturing process).
- Conducting analyses of products under development (formulation) to verify product stability over time.
Pharmaceutical stability studies under ICH conditions
Our GMP laboratory conducts stability studies as part of development projects or post-marketing surveillance. We offer substantial storage capacity in climate-controlled chambers under ICH conditions for initial stability (real-time or accelerated) or ongoing stability. We provide bespoke advice and develop specific stability study protocols.
What are the temperatures and humidity levels in our climate-controlled chambers?
- 25°C / 60% RH
- 30°C / 65% RH
- 40°C / 75% RH
Our climate-controlled chambers are under 24/7 surveillance with pharmaceutical on-call monitoring
Quality Control
Our Quality Control laboratory guarantees the compliance and quality of products, from raw materials through to finished goods. Our quality control team provides on-demand services and is also equipped to handle large-scale analysis projects, including physicochemical tests, identifications, and dosage assessments.
