Specipig has experience in running drug development in-vivo pig studies to overcome the regulatory requirements. Such as efficacy or proof of concept trials, pharmacokinetic trials, multi dose tolerance studies, toxicology studies and skin tolerance trials.
All under GLP certification.
Our aim is to accompany our partners all along the process, from the very beginning of the preclinical phase, overcoming the regulatory requirements.
R&D
- R&D development
- Proof of concept
- Efficacy validation
- Product testing
- Additive/nutritional trials
Preclinical studies
- In-vivo swine model studies
- Efficacy studies
- Safety studies
Regulatory preclinical studies
- GLP
- Toxicity studies: in-vivo toxicity and tolerance
- Dose testing