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Sunday, August 8, 2010

PATHOPHYSIOLOGY PHARMCY SUBJECTS,THEIR TOPICS AND TEXT BOOKS AND REFERANCE BOOKS

PATHOPHYSIOLOGY PHARMCY SUBJECTS,THEIR TOPICS AND TEXT BOOKS AND REFERANCE BOOKS
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PATHOPHYSIOLOGY
Text books
a. Pathologic basis of disease by- Cotran, Kumar, Robbins
b. Text book of Pathology- Harsh Mohan
c. Text book of Pathology- Y.M. Bhinde

Reference books
a. Clinical Pharmacy and Therapeutics; Second edition; Roger Walker; Churchill
Livingstone publication

1 Basic principles of cell injury and Adaptation
a) Causes, Pathogenesis and morphology of cell injury
b) Abnormalities in lipoproteinaemia, glycogen infiltration and glycogen infiltration and
glycogen infiltration and glycogen storage diseases

2 Inflammation
a) Pathogenesis of acute inflammation, Chemical mediators in inflammation, Types of chronic inflammation
b) Repairs of wounds in the skin, factors influencing healing of wounds

3 Diseases of Immunity
a) Introduction to Tand B cells
b) MHC proteins or transplantation antigens
c) Immune tolerance -
Hypersensitivity
Hypersensitivity type I, II, III, IV, Biological significance, Allergy due to food,chemicals and drugs
- Autoimmunity
Criteria for autoimmunity, Classifications of autoimmune diseases in man,
mechanism of autoimmunity, Transplantation and immunologic tolerance, allograft rejections, transplantation antigens, mechanism of rejection of allograft.
- Acquired immune deficiency syndrome (AIDS)
- Amylodosis

4 Cancer: differences between benign and malignant tumors, Histological
diagnosis of malignancy, invasions and metastasis, patterns of spread,
disturbances of growth of cells, classification of tumors, general biology of tumors, spread of malignant tumors, etiology and pathogenesis of cancer.
5 Types of shock, mechanisms, stages and management
6 Biological effects of radiation
7 Environmental and nutritional diseases
i) Air pollution and smoking- SO2,NO, NO2, and CO
ii) Protein calorie malnutrition, vitamins, obesity, pathogenesis of
starvation.
8 Pathophysiology of common diseases
a. Parkinsonism
b. Schizophrenia
c. Depression and mania
d. Hypertension,
e. Stroke (ischaemic and hemorrhage)
f. Angina, CCF, Atherosclerosis, Myocardial infarction
g. Diabetes Mellitus
h. Peptic ulcer and inflammatory bowel diseases
i. Cirrhosis and Alcoholic liver diseases
j. Acute and chronic renal failure
k. Asthma and chronic obstructive airway diseases
9 Infectious diseases :
Sexually transmitted diseases (HIV,Syphilis,Gonorrhea), Urinary tract
infections, Pneumonia, Typhoid, Tuberculosis, Leprosy, Malaria Dysentery
(bacterial and amoebic ), Hepatitis- infective hepatitis.

1 Chemical Mediators of inflammation
2 Drug Hypersensitivity
3 Cigarette smoking , its ill effects
4 Biological Effects of Radiation
5 Etiology and hazards of obesity
6 Complications of diabetes
7 Diagnosis of cancer
8 Disorders of vitamins
9 Methods in Pathology-Laboratory values of clinical significance
10 Pathophysiology of Dengue Hemorrhagic Fever (DHF)

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Do you know now this website has become a most popular and most referred website in pharmaceutical industry and pharmaceutical companies all over the world ,for almost all topics related to Pharmaceutical Manufacturing , Pharmaceutical Regulatory Affairs and Good Manufacturing Practice and latest news and new drugs developments.
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What is What is 510(k) Clearances ?
What is 510(k) Clearances,

Premarket Notification for medical devices - PMN or 510(k)

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Examples of drug interactions


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Antibiotic resitance and Antibiotic resistance mechanism

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http://whoguideline.blogspot.com/2010/04/terminalogy-and-their-explanations.html

Pharmaceutical Aseptic Manufacturing Process Terms , Terminology and Definitions.

http://whoguideline.blogspot.com/2010/02/pharmaceutical-aseptic-manufacturing.html

Here are some articles which will be useful for you in further understanding of aspects of sterile dosage form manufacturing and regulatory affairs and good manufacturing practice in

pharmaceutical industry

Pharmaceutical Validation

Types of validations in pharmaceutical manufacturing


Requirements of documents for validation of sterilisation process

How to investigate OOS out of specification results

Determination of Phenol coefficient of a disinfectant

Sterility testing

Cleen Room Classification

Time limitations in sterile pharmaceuticals processing

Aspects of validation of manufacturing process in sterile pharmaceuticals

Clinical Trials

Controlling Pyrogens in injectable dosage forms

Media fill run process simulation aspects Validation of Aseptic Process and Sterilisation

New Drug Application (NDA) how to make a New Drug Application (NDA) to US FDA

Abbreviated New Drug Application (ANDA) What is ANDA , detaied information about ANDA preparation and submission to US FDA

How to make Investigational New Drug (IND) Application to US FDA

Drug applications submission to us fda Over the counter Drugs OTC drugs

BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS

Electronic record in pharmaceutical manufacturing industry

Good manufacturing practice in pharmaceutical industry

Pharmaceutical industry pharmaceutical companies and FDA latest updates


Here is an interesting article on world wide pharmaceutical industry
Article on Pharmaceutical Industry pharmaceutical industry

Here are some interesting articles on Quality assurance systems for pharmaceutical company

1.Quality assurance in pharma industry

2.Quality by designe concept for pharmaceutical industry

3.Quality by designe concept in pharmaceutical industryan explanation

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