Compare 6 listed pharmaceuticals manufacturer profiles in Maine 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.
BBI Solutions Maine is a leading life sciences and in vitro diagnostic reagents manufacturer headquartered in Portland, ME, with over 70 years of expe...
FHC Inc is a leading manufacturer of precision neurosurgical and neurological medical devices based in Bowdoin, Maine. Since its establishment, the co...
ImmuCell Corporation, headquartered in Portland, Maine, is a pioneering pharmaceutical manufacturing company specializing in innovative colostrum-base...
Lonza Rockland Inc is a leading bioscience manufacturing facility located in Rockland, Maine, specializing in molecular biology research products and ...
Northeast Laboratory Services (NEL) stands as Maine's largest laboratory service provider, delivering comprehensive testing solutions from their facil...
Leading provider of in vitro diagnostic products and solutions for the healthcare industry. Specializes in ASSURANCE product line with high quality, h...
Compare listed pharmaceuticals manufacturer profiles in Maine 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.
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