For Global Markets
We can partner with your firm on a green field build-out, Optimization and improvement of a current facility, or qualification to a USFDA, UKMHRA or equivalent regulatory standard. We are committed to a long term approach for helping qualify any pharmaceutical firm reach their full potential.
Our Science team will train to any grade facility.Technology transfer of pharmaceutically stable products including transfer of validated analytical methods, share stability testing reports of development batches and provide support for dossier compilation.
LODAAT has developed a proprietary extraction process for our branded botanical ingredients. Our cutting-edge extraction technology termed enables the highest quality botanical extracts. We manufacture both Powder and Direct Compression (DC) Granules for Contract manufacturers, Sports and CPG firms. Many products have Clinical Trials and Double-Blinded Placebo Control Documentation.
For emerging markets, we manufacture a wide variety of Off-patent Generic drugs under the LODAAT brand and private label. With over a 1000 allopathic dosage formulations, we cover all major finished formulations and therapeutic categories.
LODAAT manufactures a full range of finished Nutraceutical products including
Our nutraceuticals support a wide range of health indications including, energy, sexual health, and weight loss. We have developed our own proprietary formulations and manufacturing process for our branded ingredients.
With a 25 member regulatory team, we are able to create dossiers including CTD, DMF, US DMFs, COS and other registrations required in various markets.dossiers that include bio-equivalency, and comparative studies.
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