Veterinary pharmaceuticals

Testing and analysis for batch release and registration
Customers in the veterinary medicinal industry benefit from RegiLabs’ extensive experience in this sector. Our pharmaceutical laboratory conducts extensive tests of raw materials and drug products to support batch release and end product registration in Europe, wherever your business is based. We ensure your products meet the requirements of international pharmacopoeia such as the European Pharmacopoeia (EP), the British Pharmacopoeia (BP), the United States Pharmacopoeia (USP), and any other protocols you may stipulate.

Stability studies
You can also entrust us with all necessary stability testing, which we conduct using our in-house temperature- and humidity-controlled chambers, in accordance with ICH guidelines.

Method development and validation
In addition to validating your analytical methods, we also put our expertise at your disposal to develop new methods in partnership with you.

Microbiological testing and advice
You can consult RegiLabs for expert advice, troubleshooting, brainstorming or method development with regard to microbiological testing. We conduct and validate a full range of tests, including total viable aerobic count, tests for specified micro-organisms, efficacy of antimicrobial preservation tests (challenge tests), LAL testing of endotoxins and microbiological assay of antibiotics, as well as identifying micro-organisms.

From the laboratory to market
Wherever you are based, our extensive network of partners can help you bring your products successfully to market in Europe. Working closely together with top-quality specialists in pharmaceutical registration, transport, storage, distribution and packaging, we can ensure your expansion into Europe is both rapid and cost-effective.