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Sunday, August 8, 2010

PHARMACEUTICS PHARMACY SUBJECTS,THEIR TOPICS AND TEXT BOOKS AND REFERANCE BOOKS PHARMACEUTICS

PHARMCY SUBJECTS,THEIR TOPICS AND TEXT BOOKS AND REFERANCE BOOKS PHARMACEUTICS
PHARMACEUTICS
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Text books
a. Cooper and Gunns Dispensing for pharmacy students.
b. A text book Professional Pharmacy by N.K.Jain and S.N.Sharma.

Reference books
a. Introduction to Pharmaceutical dosage forms by Howard C. Ansel.
b. Remington’s Pharmaceutical Sciences.
c. Register of General Pharmacy by Cooper and Gunn.
d. General Pharmacy by M.L.Schroff.

1 a. Introduction to dosage forms - classification and definitions
b. Prescription: definition, parts and handling
c. Posology: Definition, Factors affecting dose selection. Calculation of children and infant doses.
2 Historical back ground and development of profession of pharmacy and pharmaceutical industry in brief.
3 Development of Indian Pharmacopoeia and introduction to other Pharmacopoeias such as BP, USP, European Pharmacopoeia, Extra pharmacopoeia and Indian national formulary.
4 Weights and measures, Calculations involving percentage solutions, allegation, proof
spirit, isotonic solutions etc.
5 Powders and Granules: Classification advantages and disadvantages, Preparation of
simple, compound powders, Insufflations, Dusting powders, Eutectic and Explosive powders, Tooth powder and effervescent powders and granules.
6 Monophasic Dosage forms: Theoretical aspects of formulation including adjuvant like stabilizers, colorants, flavours with examples. Study of Monophasic liquids like gargles, mouth washes, Throat paint, Ear drops, Nasal drops, Liniments and lotions, Enemas and collodions.

7 Biphasic dosage forms: Suspensions and emulsions, Definition, advantages and disadvantages, classification, test for the type of emulsion, formulation, stability and evaluation.

8 Suppositories and pessaries: Definition, advantages and disadvantages, types of base, method of preparation, Displacement value and evaluation.
9 Galenicals: Definition, equipment for different extraction processes like infusion,
Decoction, Maceration and Percolation, methods of preparation of spirits, tinctures and extracts.
10 Pharmaceutical calculations.
11 Surgical aids: Surgical dressings, absorbable gelatin sponge, sutures, ligatures and
medicated bandages.
12 Incompatibilities: Introduction, classification and methods to overcome the incompatibilities.

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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)

What is a drug interaction

Examples of drug interactions


Antibiotic Definition and classification


Antibiotic resitance and Antibiotic resistance mechanism

Antioxidants food suppliments

Vitamin D Details on FDA cautions on accurate dosage of Vitamin D


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Enzyme linked immunosorbent assay ELISA

Raido Immuno assay

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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