Groupe PARIMA

Development and manufacturing of non-sterile liquid, suspensions, and semi-solid pharmaceutical products.

General Information
Company Name
Groupe PARIMA
Founded Year
1994
Location (Offices)
Montreal, Canada +1
Founders / Decision Makers
Number of Employees
68
Industries
Manufacturing, Pharmaceutical
Funding Stage
-
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Groupe PARIMA - Company Profile

Groupe PARIMA

Groupe PARIMA is a Contract Development and Manufacturing Organization (CDMO) founded in 1994 in Canada. The company specializes in the development and manufacturing of non-sterile liquids, suspensions, and semi-solid drug products. Their strategic focus on these specific areas has allowed them to establish unique expertise to support product development and manufacturing needs. Additionally, Groupe PARIMA has expanded its capabilities to include handling low-flash point mixtures and packaging metered-dose sprays, towelettes, and sachet/stick/packs.

The company operates as a 100% free-for-service business, exclusively providing contract services with a commitment not to compete with its clients. Groupe PARIMA has received favorable inspections from the European, US, Turkish, and Canadian health authorities and currently manufactures products for markets in over 30 countries.

Groupe PARIMA's services include product development such as formulation and packaging development, QbD, process scale-up, validation, and project management. They also offer analytical testing for various parameters and commercial manufacturing for several regions including the USA, Europe, Canada, Turkey, South America, Mexico, Australia, New Zealand, and MENA. The company's capabilities also cover serialization and cold-chain logistics.

With expertise in manufacturing a range of pharmaceutical products and specialized packaging, Groupe PARIMA offers solutions for creams, ointments, lotions, gels, solutions, liquids, suspensions, and flammable products. Their packaging options include bottles, jars, sprays, pumps, tubes, and specialized delivery systems like nasal sprays, sublingual sprays, and sachets/stick packs in an inert atmosphere.

Taxonomy: CDMO, Contract Development and Manufacturing Organization, Pharmaceutical Manufacturing, Formulation Development, Packaging Development, Quality by Design, Process Scale-Up, Process Validation, Analytical Testing, Commercial Manufacturing, Serialization, Cold Chain, Microbiology Testing, Non-Sterile Pharmaceutical Products, Health Authorities Compliance

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