Groupe PARIMA
Louis-David Cantin has over 17 years of experience in the pharmaceutical industry. From 2001 to 2007, they worked at Bayer Healthcare, starting as a Research Scientist and eventually becoming a Senior Research Scientist II. During this time, they managed the chemical inventory and purchasing, was a Project Chemistry Leader and R&D Project Co-Leader, and led an international IT project-team. In 2007, they moved to AstraZeneca as an Assistant Director of Medicinal Chemistry. In 2012, they became an Advisor to the CEO at gIcare pharma inc. Since 2013, they have been President of Groupe PARIMA Inc, a Development and Manufacturing Organization (CDMO) specialized in the development and manufacturing of pharmaceutical products. In this role, they oversee product development activities and quality control activities, as well as client relations, compliance and P&L. Louis-David is also responsible for the elaboration and execution of the marketing strategy.
Louis-David Cantin obtained a Diploma of Collegiate Education from Collège Jean-de-Brébeuf in 1989-1991, followed by a B.Sc. in Chemistry and Biology from Eckerd College in 1991-1994. Louis-David then completed a M.Sc. and Ph.D. in Organic Chemistry from Université de Montréal in 1994-1999, and a Post. Doc in Organic Chemistry from the University of Pennsylvania in 1999-2001. Finally, they obtained an MBA from École des sciences de la gestion (ESG UQAM) in 2012-2014.
Groupe PARIMA
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Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO), established in 1994. We have developed an expertise in the development and manufacturing of non-sterile liquids, suspensions, and semi-solid drug products. This strategic focus has allowed us to establish a unique expertise to support your product development and manufacturing needs, which, combined to our operational flexibility and commitment to delivering on time, enables us to operate as an extension of your team. Over the years, we have added specialized capabilities such as handling of low-flash point mixtures, and packaging metered-dose sprays (nasal or sublingual), towelettes and sachet/stick/packs. Our business is 100% free-for-service and exclusively focused on contract services. We are here to help you meet your company objectives, not to compete with you. We have been favorably inspected by the European, US, Turkish and Canadian health authorities, and we are manufacturing products for markets in over 30 countries. Product Development: Formulation Development, Packaging Development, QbD, Process Scale-up, process validation, project management Analytical Testing: IVRT, HPLC, UPLC, LCMS, Particle Size, Microbiology, Viscosity Commercial manufacturing for USA, Europe, Canada Turkey, South America, Mexico, Australia, New Zealand, MENA; Serialization, cold-chain Manufacturing: creams, ointments, lotions, gels, solutions, liquids, suspensions, flammable products (Antiseptic gel), inert atmosphere Packaging: Bottles, Jars, Sprays, Pumps, Tubes, Airless Pumps Pledgets/towelettes, Nasal Sprays, Sublingual Sprays, Metered-dose delivery, Syringe applicator (non-sterile), sachets and Stick packs, inert atmosphere