Compare 7 listed pharmaceuticals manufacturer profiles in Utah by process fit, location, and documented capabilities.
Results are ordered alphabetically. Inclusion is based on the matching process or industry recorded on each published profile.
Leading contract manufacturer with 61 employees in 104,000 sq ft facility. cGMP, FDA, NSF, and Kosher certified specializing in supplements including ...
Deseret Laboratories, Inc. stands as a premier pharmaceutical and nutraceutical manufacturing company based in Saint George, Utah. This full-service c...
High-speed supplement manufacturing facility since 2013 with 201-500 employees. FDA registered, NSF and SQF certified with capability to produce 27 mi...
Turnkey contract manufacturer since 2019 with 30,000 sq ft facility. cGMP, USDA Organic, and hemp certified. Ranked #125 Fastest-Growing Private Compa...
cGMP certified supplement contract manufacturer since 2015 with 21 employees. Specializes in custom capsule, powder, stick pack, and sachet production...
Nutritional contract manufacturer with 99 employees and $24.8 million revenue. FDA, NSF, and CCOF certified facility offering comprehensive manufactur...
GMP and FDA certified private-label nutraceuticals manufacturer with 5 employees. Innovation hub focusing on traditional gummies, center-filled gummie...
Compare listed pharmaceuticals manufacturer profiles in Utah by process fit, location, and the documentation the buyer can actually verify.
A pharmaceutical manufacturer can be a commercial plant, a packager, or a development lab. Choose the site type before comparing listed profiles.
| When this is the job | Use | Why |
|---|---|---|
| Commercial finished-dose supply with batch records and release testing | cGMP finished-dose manufacturer | The award depends on registered process, documentation, and inspection history. |
| Primary or secondary packaging, serialization, or labeling only | Pharmaceutical packager | The product is already made; the constraint is coding, artwork, and distribution-ready pack-out. |
| Clinical, scale-up, or formulation development before commercial transfer | Development or CDMO site | The buyer needs process development and tech-transfer evidence, not only commercial volume. |
Use a pharmaceutical manufacturer when cGMP, FDA registration, dosage form, contamination control, and batch documentation—not general contract manufacturing capacity—are the buying criteria.
Start with dosage form, registration, and quality-system scope. Then compare which operations are on site, what batch records look like, and whether the site is set up for clinical or commercial supply. Directory listing is not an FDA approval.
New Jersey, Pennsylvania, North Carolina, Illinois, and Massachusetts are the first UNITEMFG state-and-category pages to open. California remains important for specialty, clinical, and West Coast packaging work.
Our directory makes it easy to research listed manufacturing companies.