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Manufacturing companies in Latvia

3 manufacturing profiles in Latvia. Every profile is hand-reviewed with leadership, certifications, and public sources.

Profiles3
Verified3
With certifications3
Cities2
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Where does manufacturing cluster in Latvia?

Riga (2) and Marupe (1) Most visible profiles: Kalceks, Lotos Pharma, and Silvanols.

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Which standards are already visible?

GMP (3) Latest review: 21 March 2026. Review cycle: March 2026.

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Manufacturing profiles in Latvia

3 profiles match the active filter.

Current review cycle

Kalceks

RigaLatviaManufacturing

Riga pharmaceutical manufacturer developing, producing, registering, and distributing sterile hospital medicines and other finished dosage forms for international markets.

Lead
Egils KopstalsChairman of the Board
Scale
International finished-dosage manufacturing
0 sources72d reviewGMP requirementsISO certificationsICH guidelines
Current review cycle

Lotos Pharma

MarupeLatviaManufacturing

Latvian pharmaceutical manufacturing platform in Marupe combining GMP-backed production, consumer health formulations, and locally developed bio-product lines.

Lead
Kaspars IvanovsHead of Company
Scale
Commercial manufacturing
Current review cycle

Silvanols

RigaLatviaManufacturing

Riga phytopharma manufacturer combining herbal formulation expertise, GMP-backed production, and regional natural-products manufacturing capacity.

Lead
Liene PurinaMember of the Board
Scale
Regional Supply
Related brief

Read deeper on this category

Market brief

BIO CITY Vilnius: Northway Biotech’s Biotechnology City Outside Vilnius — Capabilities, Anchor Tenant, and the 2026 Build-Out

What the BIO CITY biotechnology city in Vilnius is, how Northway Biotech operates as the 2026 anchor tenant, which capabilities are live at BIO CITY Vilnius today, and how the multi-phase biotech city build-out is progressing — with sources.

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FAQ

Frequently asked questions on this category

What is the difference between a manufacturer and a CDMO?
A manufacturer primarily produces its own drug substance, drug product, or device for its own pipeline or commercial supply. A CDMO (Contract Development and Manufacturing Organization) takes external programs from other companies — process transfer, scale-up, contract production. Some companies operate as both: manufacturing their own pipeline AND offering excess capacity to external clients.
Which European countries have the most manufacturing capacity?
Germany leads by industrial depth (Boehringer Ingelheim, Bayer, BioNTech production, Merck KGaA). Switzerland concentrates premium-tier sites (Roche, Novartis manufacturing). Denmark anchors aseptic/biologics scale (Novo Nordisk). Sweden adds AstraZeneca's Gothenburg base. Poland is competitive on cost (Polpharma, Adamed). Lithuania and Estonia have growing biologics manufacturing (Northway, Icosagen).
What certifications should a biotech manufacturer hold?
For drugs and biologics: GMP (essential, country-specific national authority enforces in EU). For medical devices: ISO 13485 + CE marking under MDR/IVDR. For US-bound supply: FDA inspection. For nonclinical studies: GLP. Use the /compliance pages on this directory to filter by specific markers — every published company has its certification context documented and source-backed.
How are manufacturers verified in this directory?
Every profile is hand-reviewed: leadership confirmed by primary source, physical site address sourced from official disclosures, regulatory matrix (GMP / ISO-13485 / GLP / FDA-Inspected) backed by certification documents, and a registry note explaining current operating context and production scope.
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