We understand the challenges of modern product development and thrive on the opportunity to provide customers creative solutions based on experience, market understanding and cutting-edge science.
Our most valued asset is our team of proficient specialists whose combined expertise encompasses all aspects of pharmaceutical development and operations.
From small runs for new cosmetic products to mega-runs for established and growing brands, we can meet your manufacturing needs with fill capacities from .5 ml to >1 L.
We utilize top third party, independent laboratory specialists which enables us to ensure quality of results.
We provide cGMP manufacturing from 10 L to 7,500 L batch sizes with the flexibility to process aqueous, anhydrous and emulsion-based formulations across a wide viscosity range and under an assortment of conditions.
From raw materials to finished products, the analytical lab ensures all aspects of production quality are on target and the specifications for each product are met.
All of our goods and services are available for export, and our team of experts will assist you with the necessary paperwork and documentation to help you expand your business around the world.
Our regulatory group is experienced in providing assistance to large, mid-sized and start-up cosmetic and skincare companies. We routinely interact with FDA and other regulatory agencies on behalf of our customers and stay current on regulatory requirements and industry trends.
Our product development scientists perform critical experimentation to determine the physicochemical characteristics of the drug substance with the goal of designing optimum drug delivery systems.
Commercial volume manufacturing of solid-dose products with Single and Tri-layer tablet compression capabilities.
Our coating services are tailored for large volume commercial products. Our state-of-the-art coating equipment is cGMP compliant.
We offer a comprehensive package of analytical services to support product development.
IND, NDA, ANDA submissions. Foreign Facility and Product Registration. Post approval change consultation.