In addition, all the subjects received Caltrate D (calcium plus 125 IU cholecalciferol) daily in the form of one pill. The subjects were divided into 2 groups based on the age and serum 25(OH)D concentration: 50 subjects (group A) received cholecalciferol (800 IU/d), and 50 subjects (group B) received calcitriol (0.25 μg/d) for 3 months. One hundred Chinese postmenopausal women aged 63.8☗.0 years and with serum 25-hydroxyvitamin D concentration <30 ng/mL were recruited. The Material is not recombinant and do not contain any genes associated with livestock or poultry (or livestock or poultry diseases).To compare the effects of cholecalciferol (800 IU/d) and calcitriol (0.25 μg/d) on calcium metabolism and bone turnover in Chinese postmenopausal women with vitamin D insufficiency. The Material is not immunogen and does not come from a facility where work with any viruses is done. All documents as per pharmacopeia specification including MSDS/SDS, SER REPORT, COA, HPLC, MASS, 13CNMR, 1HNMR and TGA potency (Upto 800 deg c) and are acceptable to all various regulatory authorities such as ICH, USFDA, Canadian Drug and Health Agency & also used for ANDA filing /DMF filing and genotoxic study The materials are used purely for Testing, R & D and analytical Research Purposes and the Material is not from livestock or avian species and has not been exposed to livestock or avian disease agents. And are delivered and packaged according to regulations and Non-Infectious Biology Material and is purely for research purpose only not for human consumption. Documents - COA, HNMR, 13CNMR, MASS, HPLC (by pharmacopoeia method with RT RRT results), IR and TGA will be provided with the purchase of Cholecalciferol EP Impurity B / Provitamin D3 is manufactured by ALLMPUS LABORATRIES PVT.
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