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


Pharmaceutical

Groupe PARIMA

Lyson Nadeau

Andrea Chen

Louis-David Cantin

Riccardo Santopietro

Claude Mongrain

Rinaldo di Meglio

Anis Chalal

Hector Fabian Castro.

Peter Herskovits

Alireza Sami Seresht

Céline Gauthier

Dominique Chan

Elham K.

Hamida Ibrahim

Nathalie Lemieux

Zahia Hamma H.

The Operations Team at Groupe PARIMA is responsible for overseeing and optimizing the production processes of non-sterile liquids, suspensions, and semi-solid drug products. They ensure efficient utilization of resources, maintain high standards of quality and compliance with health regulations, and coordinate the workflow from manufacturing to packaging. Through strategic planning and effective management, the team supports timely delivery and operational flexibility, positioning Groupe PARIMA as a reliable partner for its clients' product development and manufacturing needs.

Operations Team

Quality Assurance Team

Research and Development Team

Operations Team

About

Team members

Other teams at Groupe PARIMA

Quality Assurance Team

Research and Development Team