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© 2026 cohaga AG · All Rights Reserved · St. Gallen, Switzerland · Imprint744,962 companies indexed · Last updated: today
DirectoryIndustryPharmaceutical IndustryMannoRivopharm SA
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Rivopharm SA

Summary

About the company

The core activity of Rivopharm is the development, manufacture and marketing of pharmaceutical products, including generic and branded medicines, dietary supplements and other health products. The company also provides services such as product formulation, packaging and regulatory affairs, and operates in more than 60 countries worldwide.

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Industry:Pharmaceutical Industry
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Prescription generic medicines (Rx)
Prescription generic medicines in oral dosage forms for chronic and acute treatments; tablets, capsules, blister and bottle packaging, across many therapeutic areas.
Over-the-counter (OTC) medicines
OTC medicines in oral dosage forms, in particular tablets and capsules, offered with blister and bottle packaging for various everyday needs.
Dietary supplements
Dietary supplements in different oral forms, with capsules, tablets, vials and drops; range including products for skin, heart, sleep, eyes and joints.
Pharmaceutical manufacturing and packaging
Manufacture of oral solid dosage forms, packaging of tablets and capsules, blister and bottle filling, with facilities inspected and approved by Swiss authorities and the FDA.
Analytical development and validation
Analytical development and validation for pharmaceutical products, supporting the development and industrialisation of formulations.
Pharmaceutical formulation development
Pharmaceutical formulation development, including modified-release dosage forms, with in-house services and co-development projects.
Scale-up and process development
Scale-up, process development and validation for pharmaceutical production, from development transfer to manufacturing.
QC analysis and release
Quality control analyses and product release, integrated into the pharmaceutical manufacturing and validation workflow.
Contract pharmaceutical packaging
Packaging of pharmaceutical oral dosage forms in blisters and/or bottles for clients’ formulations, with flexibility on dosing technologies.
Regulatory affairs and registration
Regulatory support, national submission or DCP procedure, coordinating approval and product registration to reduce time to market.
Direct commercialisation in selected markets
Direct commercialisation of the products in selected countries, in addition to sales via partners and customers.
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Location

Hier entsteht die Karte
Centro Insema
6928 Manno

At a glance

Legal form
Corporation
UID
CHE-102.401.066
Founded
1961 · 65 years
Last commercial register change
February 19, 2026
Employees
1 to 10

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