Your Trusted CDMO Partner

Curida is a trusted CDMO based in Norway, offering end-to-end development and contract manufacturing of biologics and sterile or non-sterile liquid pharmaceuticals. With over 50 years of expertise in Blow-Fill-Seal and Nasal Spray technologies, we support everything from formulation and tech transfer to commercial scale-up. Our Bio-CDMO unit provides manufacturing of monoclonal antibodies for preclinical and diagnostic use.

Our Values

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Flexible

We adapt, take initiative, and support our partners with empathy and openness.
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Enthusiastic

We show up with energy, listen carefully, and celebrate shared success.
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Trustworthy

We deliver with integrity, quality, and accountability—every time.
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Bold

We speak up, embrace change, and act with confidence to drive innovation.

Our Story

The "Pillefabrikken" is born
Norsk Medisinaldepot (NAF) establishes a site focused on tablets, liquids, and sterile solutions.

1974

Ås pharmacy is founded
Pharmacist Kjell-Erik Andersen opens the pharmacy in Ås.
Elverum Site
Elverum site acquired by Norsk Hydro

1987

Diatec founded as a diagnostic distributor
Quickly expands to develop in-house diagnostic kits and monoclonal antibodies.

1988

Elverum site acquired by Nycomed
The plant specialises in sterile liquids and ampoules.

1992

Ås Produksjonslab is founded
Becomes a dedicated production department focused on liquids.
Diatec restructuring
Diatec restructures to focus on monoclonal antibody services

2003

Takeda acquires Elverum site
Becomes part of the global Takeda network.
Diatec's first clinical-phase
Diatec manufactures its first clinical-phase API for a cancer drug

2011

Diatec gets certified
Diatec achieves GMP certification

2014

Curida is born
Employees volunteer over 10,000 hours to revive the Elverum site.

2015

New investors, shared vision
Norwegian family offices and Investinor invest in Curida.

2017

Ås Produksjonslab joins Curida
Strengthens Curida’s connection to the Norwegian pharmacy industry.

2018

Diatec upgrades GMP facility
Redesigned for flexibility and operational efficiency.

2019

Curida acquires Diatec Monoclonals
Expands Curida's biologics and monoclonal antibody capabilities.

2022

A new look for Curida
The new Consolidated Curida Brand & Website is launched

2025

Want to Work with us?

We are always on the lookout for talented people with a Life Science background.

Careers

Committed to GMP Excellence

We put quality and patient safety at the heart of everything we do. Operating under EU GMP and ISO 13485:2016, our teams ensure sterility, consistency, and full compliance. From seamless tech transfer to aseptic manufacturing, we follow recognised best practices to deliver trusted pharmaceuticals and products—every step of the way.

Find out more from one of our key services.

Contract Manufacturing

Our Certifications

Curida operates to the highest regulatory standards across all facilities. Our certifications reflect our commitment to compliance, quality, and traceability in every aspect of pharmaceutical manufacturing.
ISO 13485

Our Liquid Formulations site is ISO 13485 certified, ensuring consistent, high-quality products.

ISO 9001

Our Biologics site is ISO 9001:2015 certified, demonstrating our commitment to robust quality management practices.

GMP Certified

Curida is EU GMP certified for Liquid Formulation manufacturing.

ISPE Good Practice

We follow the ISPE Good Practice Guide for Technology Transfer to ensure compliant and consistent product transfers.

Code of Conduct

At Curida, ethics is about how we treat each other, our partners, and the world around us. Our Code of Conduct is the foundation of how we work — guiding our decisions, shaping our culture, and helping us do what’s right.
It sets clear expectations for how we act, both inside the company and with those we work with. It’s not just a document — it’s a reminder to stay mindful, responsible, and professional in everything we do.

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