The primary aim of carrying out stability studies of drug products is to determine the expiration date and to promise the product standardized for efficacy, safety and elegance throughout its shelf-life. ICH, WHO, ASEAN and separate agencies issued the guidelines for stability studies, which are requisite to be demeanour in a deliberate way and are wise as pre-requisite for regulatory fill and approval of any medicinal product. Stability investigating provides the collection on stability strikingness of drug product including the belief of various environmental factors, packaging method etc. ensuring that it remain within planted specification to hold its degree and present the desirable performance consistently and in a way comforting for the usefulness of its intentional use all finished the retest or expiry date. This canvas types of stability studies, guidelines issue for stability investigation and forecasting of shelf life of medicine products along with flowing trends in stability studies.
All Pharmaceutical industries endeavour to produce good quality products which are achieved by allowing in-process and finished product quality control approaches. In-process quality control is concepts that are carried out before, after and during production covering all steps, counting the establishment of specifications, sampling, relevant testing and analytical clearance assuring that the intermediates, packaging materials and finished pharmaceutical tablets conform with approved specifications or standard for efficacy, safety and elegance which assure the consumer that the products perform consistently and in a manner satisfactory for the purpose for which it is recommended. Quality control highlights testing of products for defects which ease the producer to refuse the releases of products or carry out the possible investigation to make pharmaceutical tablets perfect before released into the market. Since different pharmacopoeias have set the diverse specified limits to some extent within which the value ought to fall with respect to be acquiescent as per the standards. Hence by comparing pharmacopoeias, an effort is made to convey the harmonized limits so that the products should meet the requirements as specified in pharmacopoeias specification to confirm the quality of pharmaceutical dosage form. The endeavour of this study is to compare various quality control assessments for pharmaceutical tablets according to different pharmacopoeias standards.
Whether originating from physical or mental factors, stress has been demonstrated to provoke alterations in blood sugar levels, presenting a predicament for individuals living with diabetes. Stress tends to elevate the levels of counter-regulatory hormones, particularly cortisol, adrenaline, or noradrenaline. Furthermore, diabetes itself constitutes a significant source of stress. To investigate the impact of stress on diabetes, a study was conducted with 200 participants diagnosed with Type-I and Type-II diabetes. These individuals were divided into two distinct groups based on their stress levels. A battery of tests and questionnaires was administered to both groups to assess their respective stress levels. The data collected underwent rigorous statistical analysis, which revealed that individuals diagnosed with diabetes displayed a mean stress score of 18, with a corresponding mean deviation of 12.59. This study provides compelling evidence that people living with diabetes experience significantly higher levels of stress compared to their non-diabetic counterparts. Key words: Diabetes, Type-I and Type-II diabetes, biological stress.
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