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Pharma Develops Intermediates Services In North America
5 services found
Manufactured by:Novasep based inChasse-sur-Rhône, FRANCE
We believe that the quality and transparency of communication with you and within our organization are crucial in delivering your project. Each project is attributed to a professional project manager who is your dedicated point of contact at Novasep for the whole duration of the collaboration. The project manager coordinates all activities related to your projects and liaises between the ...
by:CycleSolv based inNewark, DELAWARE (USA)
We supply a wide range of organic compounds, pharmaceuticals, intermediates, non-hazardous solvents, cleaning agents and detergents. We have the ability to deliver hard to find chemical products with competitive prices. Ordered products can be shipped from our warehouse in Wilmington, DE or directly from our ...
Manufactured by:CD Formulation based inShirley, NEW YORK (USA)
About 40% of newly developed medicinal chemical entities have poor water solubility, and 90% of drugs under development can be classified as poorly soluble drugs. A solid dispersion (SD) refers to a dispersion system in which the drug particle size is within the range of 0.001 to 0.1 μm in a certain state and uniformly dispersed in a solid carrier. As an intermediate of pharmaceutical ...
Manufactured by:Regis Technologies Inc. based inMorton Grove, ILLINOIS (USA)
Expedite your discovery-to-market timeline by partnering with Regis Technologies to produce your Active Pharmaceutical Ingredients (APIs) and intermediates. We are committed to advancing your projects from initial process development, scale-up development through final validation and commercial manufacturing. Partner with Regis to bring your regulatory starting material, pre-clinical, phase I-III ...
by:Ofni Systems Inc. based inRaleigh, NORTH CAROLINA (USA)
Process, Design, and Equipment Validation are the formal processes for establishing objective evidence that systems consistently produce results or products meeting predetermined specifications, as required by the Federal FD&C Act and cGMP. Validation is an excellent tool to understand and maximize value from your business processes. Validation is also a compliance issue; the FDA requires ...