Developed to Perform. Manufactured to Scale.
Partnering with you across development to commercial manufacturing to bring complex non‑sterile liquids, semi‑solids, and suspensions to market faster.
our partners
01
Pharmaceutical companies
You gain production flexibility to match batch sizes to your program.
02
Biotech Startups
You scale production with the right technical expertise at each stage.
Reach the World.
Our Services
Our integrated, GMP-compliant site supports the full product lifecycle, from formulation to commercial manufacturing, with flexibility and reliable execution.
Pre-Formulation Studies
Pre‑formulation studies tailored to your target profile, guided by measurable data.
Learn moreFormulation Development
Non‑sterile dosage forms designed for robust performance and consistent manufacturing
Learn moreProcess Scale-Up
Equipment aligned to deliver consistent results from engineering runs to GMP batches.
Learn moreProcess Validation
Process validation with defined criteria, controlled PPQ, and submission‑ready docs.
Learn moreMethod Development
Analytical methods tailored for stability data and simplified validation and transfer.
Learn moreMethod Validation
Validation and method transfer to support GMP QC testing and full-lifecycle use.
Learn moreRelease Testing
GMP release testing aligned with approved specifications for confident batch release.
Learn moreStability Studies
Stability studies from protocol to reporting support a confident shelf‑life assignment.
Learn moreDrug Manufacturing
Drug manufacturing with disciplined GMP execution across all production stages.
Learn moreClinical Supply
Clinical supply delivered through manufacturing and packaging aligned with GMP requirements.
Learn morePrimary & Secondary Packaging
Turn‑key primary and secondary packaging ensuring product integrity and compliance.
Learn moreLabeling & Serialization
Labeling and serialization are aligned with manufacturing for a compliant commercial supply.
Learn moreIntegrated GMP execution
Whether you’re developing a new product or scaling into a commercial production, our single‑site model ensures seamless scientific, operational, and regulatory support throughout the entire lifecycle.
01
End-to-end execution
Keep your program within a single GMP facility to streamline decision-making, minimize risk, and accelerate your path to market.
02
Scientific expertise
We serve as an extension of your team, providing access to our experts to resolve challenges faster and reinforce product robustness.
03
Flexible production
Scale seamlessly from clinical batches to commercial production, with adaptability for complex formulations and specialty programs.
04
Ongoing commitment
Proven reliability fostering long‑term partnerships to support programs across development and commercialization.
Partnerships that last
Over 30 years of operations have fostered client relationships, reflecting the trust, consistency, and collaboration we deliver at every stage.
Manufacturing
Biotech company
Analytical
Pharmaceutical company
Manufacturing
Biotech company
Analytical
Pharmaceutical company
Analytical
Pharmaceutical company
Analytical
Pharmaceutical company
careers
Join our Team
Collaborate with dedicated professionals and grow in a company that supports career development.
News and insights
Access expert insights and resources to navigate non‑sterile development and manufacturing.
2026/04/27
How Drug Product Formulation Works: Topical, Oral, and Nasal Liquid and Semi-Solid Dosage Forms
Global Regulatory Compliance
GMP operations aligned with global regulatory requirements, reducing risk and supporting submissions.
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Have a project in Pipeline?
Let’s discuss how we can confidently support your program from development through commercialization.