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Tablets dosage form different types of tablets

Tablets dosage form different types of tablets dosage form manufactured Tablet is an oral dosage form in pharmaceutical dosage forms, it is one of widely acceptable and of very great importance. One can formulate a tablet with drug amount in the range of 0.01 mg to 500 to 600 mg for human dosage and up […]

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What is Site Master File SMF

Site Master File

    1.0  SITE MASTER FILE (SMF) 1.1 What is Site Master File SMF SMF is detail information about the site. it is abbreviated as SMF SMF is a document that summarizes the firm’s overall philosophy, intentions and approach to be used for establishing registration in various countries. It is also referred as drug master […]

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Dementia treatment Sildenafil Reduces Risk of Alzheimer’s Disease

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Dementia treatment with Sildenafil Multivitamin Multimineral  Alzheimer’s disease is a disease condition associated with aging and is very critical in some patients, patients tend to forget things even their adress and homes in old age.   While it if found in a recent research done by National Institute of Health that, in an experimental models, […]

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Breast Cancer Vaccine prevent reoccurrence of barest cancer

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Vaccine that prevent re-occurrence of barest cancer:Mucin1 +Mannan (a type of sugar) complex when injected in to patient affected with breast cancer develops cellular immunity that prevents  reoccurrence of breast cancer. Brest cancer is one of most life threatening disease responsible for loss of women’s lives worldwide. It accounts to about 29.1 % of the total cancers, and […]

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How to calculate Air changes per hour ACPH in what is CFM in AHU

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What is air changes per hour What is CFM how they are related to cleanness of Pharmaceutical Manufacturing Aria What is ACPH, Air Changes per hour Importance of CFM and ACPH (air changes per hour). How ACPH is related to cleanness of room. How to calculate Air changes per hour ACPH in what is CFM […]

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USFD Guidelines WHO GMP Guidelines on Validation Requirments of Documents and Documentation

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Which documents are required to be keep updated during a Validation or Qualification Activity?  As per USFDA Guidelines, WHO GMP guidelines on Validation Which documents are required to be updated for conducting a successful validation activity. 1: Validation master Plan, should cover the present validation activity schedule and its revalidation future plan. 2. All SOPS […]

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