An Overview of Pharmaceutical Process Validation of Solid Dosage Form.
نویسندگان
چکیده
منابع مشابه
Development and Validation of Deflazacort Drug in Pharmaceutical Dosage Form
A Simple fast and precise reversed phase high performance liquid chromatographic method is developed for the Deflazacort drug. Chromatographic separation was performed a C18 column (250×4.6 mm) as a stationary phase with the mobile phase of Acetonitrile, methanol and water (90:5:5 v/v). Flow rate is 1.0 ml/min the detection of wave length is 230 nm. This method was validated for linearity, accu...
متن کاملAn Overview: the Role of Process Validation in Pharmaceutical Industry
The present review article focus on introduction and general overview on process validation in pharmaceutical industry. The word validation simply means “Assessment of validation or action of proving effectiveness”. The process is developed in such a way that the required parameters are achieved and it ensures that the output of the process will consistently meet the required parameters during ...
متن کاملIndustrial Process Validation of Tablet Dosage Form: a Review
The present article gives an introduction and general overview on process validation of pharmaceutical manufacturing process especially tablet manufacturing process. The principal objective of dosage form design is to achieve a predictable therapeutic response to a drug included in a formulation which is capable of large scale manufacture with reproducible product quality. Solid dosage forms in...
متن کاملOverview of Pharmaceutical Validation and Process Controls in Drug Development
It has always been known that facilities and processes involved in pharmaceutical production impact significantly on the quality of the products. The processes include raw material and equipment inspections as well as in-process controls. Process controls are mandatory in good manufacturing practice (GMP). The purpose is to monitor the on-line and off-line performance of the manufacturing proce...
متن کاملDetermination of Darunavir in Pharmaceutical Dosage Form
An accurate and economical spectrophotometric method for the determination of Darunavir in pure and dosage forms has been described in the present work. Stocksolution of Darunavir was prepared by initially by dissolving 100 mg of Darunavir in 10 mL of methanol and made up to 100 mL with distilled water. The values obtained by the proposed and reference method for formulations were compared stat...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Journal of Current Pharma Research
سال: 2013
ISSN: 2230-7834,2230-7842
DOI: 10.33786/jcpr.2013.v03i02.006