Month: June 2022
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Clean room classification In Pharmaceutical Industry Guidelines
Clean Room Classification in pharmaceutical Industry how it is done?. What is a clean room and clean room Classification in Pharmaceutical Manufacturing? Which are the different requirements of clean room class in pharmaceutical manufacturing ? Relation of Particle count and Viable Count requirements of different grades of Clean Rooms. Clean rooms in pharmaceutical industry are…
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Clean room classification Pharma area classification particle count Required class as per Pharma Dosage forms Tablet Oral Injection
Clean Room classification Pharmaceutical Manufacturing Area Classification particle count What is a clean room in Pharmaceutical Manufacturing,which are the different requirements of clean room class in pharmaceutical manufacturing. Introduction: Clean rooms are classified as per ISO and Federal standards 209E ISO 14644-1 and ISO 14698 is non regulatory while FED STD 209E are mandatory guideline of…
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Is it true that stress is responsible for diabetes?
Yes it is true that mental stress is responsible for developing diabetes. Why stress is responsible for diabetes? How stress can develop diabetes? Stress is associated with diabetes is very true, whenever someone is in stress, his body produces a hormone noradrenalin an anti stress hormone, but this hormone has negative effect on secretion of…
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Nanoparticles of polyethylene terephthalate PET in treatment of MRSA
Even with the advances in medicine still there are few bacterial and fungal infection which are difficult to treat as the drugs available do not always work against them, or the drugs themselves prove more toxic to body cells than to infecting microorganism, one of such is microbe is Staphylococcus aureus. Resistant form of Staphylococcus…
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Sildenafil Reduces Risk of Alzheimer's Disease
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, stem cell derived nerve cells when added…
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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 CFM What is ACPH, Air Changes per hour Importance of CFM and ACPH (air changes per hour). How ACPH is related to cleanness of room. Is it true that higher degree of clean room requires high number of ACPH? In pharma industry manufacturing facility area are classified depending up on ther requirements of…
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Revalidation in pharmaceutical manufacturing when why to do Revalidation
Periodic revalidations in pharmaceutical manufacturing its regulatory and general requirements. Validation in pharmaceutical is not only mandatory by law or regulation, but also it a is one of the method by which pharmaceutical quality assurance ensure that the drug manufactured in the firm will always meet the required quality standards. Validation is a process of…
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USFD Guidelines WHO GMP Guidelines on Validation Requirments of Documents and Documentation
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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Stem Cells use Cord blood stem cells treatment
Stem cell and regenerative medicine: What is stem cell therapy ? Which disease condition can be treated with stem cell therapy.There are certain cells in our body known as stem cells can differentiate in to many different organ tissue cells and connective tissues (pluripotent cells), which make stem cells one of great tool in regenerative medicine…
Guidelines on Pharmaceutical Manufacturing Pharma Quality Assurance Quality Management System 