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With a vast amount of experience that spans more than three decades, Porsolt conducts trials and studies pertaining to central nervous system (CNS) disorders, cardiovascular issues, pain, inflammation, gastrointestinal, obesity, oncology, predictive toxicology, and many more. “The adaptability of Porsolt’s studies is reflected through the availability of varied in-vivo models and in-vitro testing expertise used in research, along with numerous capabilities to supplement its services,” affirms Guillaume Froget, President and CEO of the company. Furthermore, to ensure that the drugs are safe for humans, Porsolt performs its studies on a wide range of living species, from mice and rats,through larger species. Porsolt’s Good Laboratory Practice (GLP) compliance and animal care accreditation (AAALAC) also ensure that any study and testing handled by the company will always follow the norms provided by regulatory bodies, to ensure quality and lessen the risk of being rejected by such bodies.
What sets Porsolt apart from the rest of its contemporaries is the direct and transparent approach the company undertakes while engaging with clients and conducting relevant studies. A continuous dialogue between the companies focuses on the direct interaction with its scientists, so the client has complete vision and awareness.
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The adaptability of Porsolt’s studies is reflected through the availability of in-vivo models and in-vitro testing expertise used in research, along with numerous capabilities to supplement its services.
What supports Porsolt’s claim of providing unique and compliant research studies is its collaboration with clients to address their specific questions, while being mindful of the regulatory quidelines. One such example involved adapting its well established and GLP compliant drug abuse capabilities to test a novel client compound. Often regulatory authorities, such as the FDA or EMA, require a similar known substance to be tested as a control alongside the test compound. Given the unique properties of the client compound, Porsolt was able to adapt the study protocol to successfully test the drug while still addressing the guidelines from the regulatory authorities. This innovative approach, utilizing Porsolt’s varied capabilities and years of experience, resulted in huge time and expenditure savings for the client.

Porsolt’s competence in developing bespoke models and conducting tailored studies is also crucial in today’s evolving drug development market. One case involved Porsolt developing a unique model for testing a client’s pain-reducing drug, by combining an established pain model together with its surgical, electrophysiology, and biomarker analysis capabilities, thereby addressing the specific needs of the client’s program.
In a bid to improve its expert services, Porsolt is aspiring to further enhance its current service portfolio towards new areas of opportunities, determined by client demands and market trends. In terms of global expansion, the company is looking forward to broadening its global presence in new and growing markets across Korea, China, India, and Eastern Europe.
Company
Porsolt
Management
Guillaume Froget, CEO
Description
Porsolt is a long-established preclinical CRO, having started
operations in 1984 under the name ITEM-Labo. Porsolt has obtained an international reputation for expertise in physiopathological models, customized procedures and tailored solutions for discovering treatments of psychiatric and neurological disorders, acute and chronic pain, inflammation, cardiac and vascular diseases, and metabolic and eating disorders. Porsolt also offers services for safety evaluation of drug candidates from screening to pre-Phase 1 regulatory studies (ICH S7), in full compliance with GLP. Porsolt’s safety program includes full assessment of arrhythmogenic risk and abuse/dependence liability.
Porsolt is headquartered in France with research facilities in Laval.