Protamine Sulfate Injection USP 250mg/25ml manufacturer in India {Taj Pharmaceuticals}

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Taj Pharmaceuticals as Manufacturer of Protamine Sulfate Injection USP 250mg/25ml Protamine Sulfate Injection USP 250mg/25ml manufacturer in India {Taj Pharmaceuticals}; best quality supplier and exporter of Protamine Sulfate Injection USP 250mg/25ml Taj Pharmaceuticals manufactures a wide range of pharmaceuticals formulation involving Ointment/Ointment/Tablets and Orals. Taj Pharma India team has an excellent expertise in manufacturing and export of Protamine Sulfate Injection USP 250mg/25ml Taj Pharmaceuticals places its main business as a Pharmaceuticals manufacturing and exports of generic drug supply of Protamine Sulfate Injection USP 250mg/25ml; primarily of pharmaceuticals preparations known as Protamine Sulfate Injection USP 250mg/25ml; as well as more than 100+ generic equivalent drug. Taj Pharmaceuticals has performed these business activities related to exports of Protamine Sulfate Injection USP 250mg/25ml for major foreign-affiliated pharmaceutical import companies, ministry of health, tenders etc. and have enjoyed the full confidence of these companies, instructions and governments. Taj Pharma Group Under close cooperation between the formulation manufacturing division, active ingredient division and the technology development division for major generic formulations such as Protamine Sulfate Injection USP 250mg/25ml; at Taj Pharma we will appropriately meet diverse needs for Protamine Sulfate Injection USP 250mg/25ml export manufacturing in a wide range of activities from investigation of possible formulations of Protamine Sulfate Injection USP 250mg/25ml, formulation development, making applications to the international regulatory authorities for marketing approval, validation of Protamine Sulfate Injection USP 250mg/25ml through to manufacturing scale production at our cGMP compliant manufacturing units of Taj Pharmaceuticals under the umbrella of Taj Pharma Group. We at Taj Pharma intend to make our manufacturing systems comply with the requirements of the FDA (cGMP) such that pilot plant scale production of products in the stage of clinical development or for use in clinical studies, as well as manufacture of products in small lots are practicable to ensure a highly stable pharmaceuticals formulations of generic equivalent and bio-similar products. We conduct extensive bio-similar and bio-equivalency studies for all our formations


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