Sunday, August 8, 2010
COMMUNITY PHARMACY PHARMCY SUBJECTS,THEIR TOPICS AND TEXT BOOKS AND REFERANCE BOOKS
GET IT AS A PDF AS YOUR PERSONAL COPY
COMMUNITY PHARMACY
Text Books:
a. Health Education and Community Pharmacy by N.S.Parmar.
b. WHO consultative group report.
c. Drug store & Business management by Mohammed Ali & Jyoti.
Reference books:
a. Handbook of pharmacy – health care.Edt. Robin J Harman. The Pharmaceutical press.
b. Comprehensive Pharmacy Review – Edt. Leon Shargel. Lippincott Williams Wilkins.
Topics
1 Definition, scope, of community pharmacy
Roles and responsibilities of Community pharmacist
2 Community Pharmacy Management
a) Selection of site, Space layout, and design
b) Staff, Materials- coding, stocking
c) Legal requirements
d) Maintenance of various registers
e) Use of Computers: Business and health care soft wares
3 Prescriptions – parts of prescription, legality & identification of medication related problems like drug interactions.
4 Inventory control in community pharmacy
Definition, various methods of Inventory Control
ABC, VED, EOQ, Lead time, safety stock
5 Pharmaceutical care
Definition and Principles of Pharmaceutical care.
6 Patient counselling
Definition, outcomes, various stages, barriers, Strategies to overcome barriers Patient information leaflets- content, design, & layouts, advisory labels
7 Patient medication adherence
Definition, Factors affecting medication adherence, role of pharmacist
in improving the adherence.
8 Health screening services
Definition, importance, methods for screening
Blood pressure/ blood sugar/ lung function
and Cholesterol testing
9 OTC Medication- Definition, OTC medication list & Counselling
10 Health Education
WHO Definition of health, and health promotion, care for children, pregnant breast feeding women, and geriatric patients.
Commonly occurring Communicable Diseases, causative agents,
Clinical presentations and prevention of communicable diseases – Tuberculosis, Hepatitis, Typhoid, Amoebiasis, Malaria, Leprosy,
Syphilis, Gonorrhea and AIDS Balance diet, and treatment & prevention of deficiency disorders Family planning – role of pharmacist
11 Responding to symptoms of minor ailments
Relevant pathophysiology, common drug therapy to, Pain, GI disturbances (Nausea, Vomiting, Dyspepsia, diarrhea, constipation), Pyrexia, Opthalmic
symptoms, worms infestations.
12 Essential Drugs concept and Rational Drug Therapy
Role of community pharmacist
13 Code of ethics for community pharmacists
=======================================================================
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.
=======================================================================
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
What is an antibody? what is monoclonal and polyclonal antibodies?
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
Latest Pharma Update
USFDA approves first drug Inmazeb to treat Ebola Virus Infection
US FDA approved first drug to treat Ebola Virus Infection (zaire ebolavirus) . So far there was no drug treatment available for Ebola virus ...


You May Also Like
-
Clean Room Classification aspects of cleanroom requirements in aseptic Process in manufacturing of sterile dosage form. Classification o...
-
Clean Room classification Pharmaceutical Manufacturing Area Classification particle count Introduction: Clean rooms are classified as per...
-
Isolators in pharma manufacturing. What is an Isolator - A decontaminated unit, supplied with Class 100 (ISO 5) or higher air quality, th...
-
Pharmaceutical validation In pharmaceutical manufacturing industry Pharma Validation regulatory requirements. Validation in Pharma Indus...
-
Corrective and Preventive Action CAPA What is meant by CAPA In Pharma As the title itself suggest CAPA is an important function of qualit...

Pharmaceutical Manufacturing Guidelines
Reverse Osmosis Membrane Technology RO Water Purification system
SOP for Mechanical Qualification of Dissolution Apparatus
Standard Operating Procedure How to write a SOP
Sterile dosage form manufacturing facility inspection
Sterility testing in sterile dosage form
Sterility testing of Pharmaceuticals dosage forms
Transdermal Drug Delivery System
Ultraviolet light as antimicrobial disinfectant in water for pharmaceutical use
Monoclonal antibodies, Polyclonal Antibodies, What are Antibodies
What is a Biosimilar or Interchangeable Biopharmaceutical
What is clinical trial protocol
Common Technical Document(CTD)
What is drug receptors?How drug resistance occur
First pass metabolism of a drug
Lyophilization Freeze Drying advantages and disadvantages of lyophilization
What is a prion, What is Mad Cow Disease
What is protein binding of drug, Why a drug is bound to protein
What is protein binding of drug, Why a drug is bound to protein
Requirements Transdermal drug delivery system
Ophthalmic Preparation |Ophthalmic solution and suspensions
Monoclonal antibodies, Polyclonal Antibodies, What are Antibodies
GO TO TOP

No comments:
Post a Comment