Expert Contract Manufacturing Services — 8 Dosage Forms, FDA-Registered
cGMP-Certified, NSF-Audited CDMO in Orange County, California — Oral Dissolving Films, Suppositories, Whitening Strips, Capsules & More. Low MOQ, In-House R&D.
Contract Manufacturing Services We Offer
Atrium Scientific Group provides expert contract manufacturing services across 8 dosage forms from a single FDA-registered, cGMP-certified facility in Orange County, California. One manufacturing partner. One quality system. Every format you need.
Where Complex Projects Get Solved
Most contract manufacturers have equipment. Atrium has process engineers. When a formula is sensitive, a dosage form is technically demanding, or a previous CDMO quietly handed the project back — that is exactly where our team begins. We built our contract manufacturing services around the formulations that expose capability gaps in less specialized facilities.
Sensitive emulsions, suppositories, oral dissolving films, sublingual strips, topical analgesics — if the dosage form is complex and the process demands precision, that is the work we are set up to do. Our in-house formulation scientists stay in the problem with you until it is solved.
From First Conversation to Commercial Production
Technical Intake
We start by understanding your formula, regulatory requirements, and where previous development efforts stalled — before recommending a path forward.
Formulation & Pilot
In-house R&D scientists develop and iterate on your formula. Our lab sits inside the manufacturing facility — iteration cycles are measured in days, not weeks.
Stability & Scale-Up
Stability protocols are designed around real-world conditions. Scale-up decisions are backed by data we generated ourselves — no third-party lab delays.
Why Brands Choose Atrium
Complex Projects Welcome
We take on the formulations other CDMOs hand back — ODF, suppositories, sensitive emulsions, and difficult oral care actives.
Faster Development Cycles
In-house testing lab inside the manufacturing facility means iteration happens in days, not weeks. No outsourcing delay between R&D and production.
Domestic Supply Chain
100% Made in USA. No overseas production delays, no compliance gaps, no import uncertainty. Brands that cannot afford supply chain risk choose Atrium.
Low MOQ, Scalable
Starting from 3,000 units for ODF strips. Launch-friendly minimums for startups and scale-up paths that keep you with one partner as volume grows.
Frequently Asked Questions
Questions about our contract manufacturing services, minimums, and capabilities. Not seeing your question? Contact our team directly — we respond within one business day.
Ready to Move Your Project Forward?
Tell us your contract manufacturing concept — dosage form, target market, and key active ingredients. Our formulation team will respond within one business day. We work exclusively with B2B clients and sign NDAs before any technical discussion.
Contract Manufacturing Services — Full FAQ
What contract manufacturing services does Atrium Scientific offer?
Atrium Scientific provides contract manufacturing services across 8 dosage forms: oral dissolving films (ODF) and sublingual strips via the HarmonyFilm™ platform, oral care products including mouth rinses, tongue gels, oral sprays, and toothpastes, rectal and vaginal suppositories, teeth whitening strips and gels, dietary supplement capsules, topical creams and gels, stick packs and powder formats, and custom formulation R&D. Both private label manufacturing and custom formulation development are available for all product categories.
What is Atrium Scientific’s minimum order quantity (MOQ)?
Atrium’s minimum order quantity starts at 3,000 units for oral dissolving film and sublingual strip formats. MOQs for other dosage forms vary — suppositories, capsules, topicals, and liquid formats each have their own minimums based on fill size and packaging format. See the full MOQ guide by dosage form for specific numbers by product category.
Does Atrium Scientific support startups and new supplement brands?
Yes. Atrium’s 3,000-unit minimum order quantity is specifically designed to be accessible to startup supplement brands, emerging DTC businesses, and companies launching their first product. Atrium’s team works with brands at all stages — including those with no prior manufacturing experience — guiding them through formulation development, regulatory classification, label requirements, and production planning.
Can Atrium Scientific manufacture products for international markets?
Yes. Atrium manufactures products for brands selling in the United States, Australia, Canada, and other international markets. The FDA-registered facility provides manufacturing documentation supporting Australian TGA GMP recognition and Health Canada NHP compliance for Canadian market entry. International brands receive the same manufacturing standards and full regulatory documentation support as domestic clients.
What is included in Atrium’s end-to-end contract manufacturing service?
Atrium’s turnkey contract manufacturing service includes custom formulation R&D, raw material sourcing and supplier qualification, prototype and pilot batch production, stability testing, in-house analytical quality control, GMP production at scale, packaging and labeling support, Certificate of Analysis documentation, and finished goods delivery. Brands can engage Atrium at any stage of the product development process.
