The document discusses concepts related to cGMP (current good manufacturing practices) and industrial management. It covers several topics related to cGMP compliance including objectives of cGMP, layout of buildings and facilities, production organization, material management, inventory management, and quality control. It also discusses concepts like plant layout, material procurement, inventory costs, and techniques for inventory management. The overall document provides an overview of various aspects involved in ensuring cGMP compliance and efficient industrial management practices.
Process Validation is Key important factor for the Pharmaceutical Industry to maintain Consistent Quality in product which claimed by the manufacturer.
Objectives and policies of c gmp, layout of building and servicesSharwari Sapate
Pharmaceutical Quality affects every individual. Therefore GMP is required to ensure the quality of the particular drug or dosage form. In this presentation you will go through some basic information about cGMP and layout of buildings.
Introduction, Regulatory requirements for validation, Role of FDA, Code of Federal regulation, Validation life cycle, Significance of validation, Types of validation, Process valiadation, Phases of process validation, Process capability design, Process Qualification, Validation maintainance phase
Types of Process validation, Examples
Objectives , policies and principles of cGMP guidelines in pharmaceutical ind...JaskiranKaur72
The presentation contains detailed information about the current GMP in the pharmaceutical industry. It has objectives , policies and principles of cGMP guidelines.
Pdf file is being attached in the link below- https://drive.google.com/file/d/11al8n8AqrkUR_Vnm-z4Mp6O0elzyniEz/view?usp=drivesdk
Master Formula Record (MFR) is a master document for any
pharmaceutical product. MFR contains all information about the manufacturing process
for the product. MFR is prepared by the research and development team of the
company. MFR is used as reference standard for preparing batch manufacturing record (BMR) by manufacturing units.
cGMP refers to Current Good Manufacturing Practices (CGMP) regulations enforced by US FDA .
CGMP are the methods to be used in ,the facilities or controls to be used for ,the manufacturing ,processing, packaging or holding of a drug to assure that such drug meets
The requirements of the act, and has the identity and strength and meets the quality and purity characteristics that is represented to possess.
Process Validation is Key important factor for the Pharmaceutical Industry to maintain Consistent Quality in product which claimed by the manufacturer.
Objectives and policies of c gmp, layout of building and servicesSharwari Sapate
Pharmaceutical Quality affects every individual. Therefore GMP is required to ensure the quality of the particular drug or dosage form. In this presentation you will go through some basic information about cGMP and layout of buildings.
Introduction, Regulatory requirements for validation, Role of FDA, Code of Federal regulation, Validation life cycle, Significance of validation, Types of validation, Process valiadation, Phases of process validation, Process capability design, Process Qualification, Validation maintainance phase
Types of Process validation, Examples
Objectives , policies and principles of cGMP guidelines in pharmaceutical ind...JaskiranKaur72
The presentation contains detailed information about the current GMP in the pharmaceutical industry. It has objectives , policies and principles of cGMP guidelines.
Pdf file is being attached in the link below- https://drive.google.com/file/d/11al8n8AqrkUR_Vnm-z4Mp6O0elzyniEz/view?usp=drivesdk
Master Formula Record (MFR) is a master document for any
pharmaceutical product. MFR contains all information about the manufacturing process
for the product. MFR is prepared by the research and development team of the
company. MFR is used as reference standard for preparing batch manufacturing record (BMR) by manufacturing units.
cGMP refers to Current Good Manufacturing Practices (CGMP) regulations enforced by US FDA .
CGMP are the methods to be used in ,the facilities or controls to be used for ,the manufacturing ,processing, packaging or holding of a drug to assure that such drug meets
The requirements of the act, and has the identity and strength and meets the quality and purity characteristics that is represented to possess.
Presented By :- Raghav Sharma
Class :- M.Pharm, 1st sem.
Department :- Pharmaceutics
Institute :- Parul Institute of Pharmacy
Content :-
Current good manufacturing Practices
Equipment and their maintenance
Production Management
Conclusion
References
Current good manufacturing practice .pptxOsamaTauseef2
Current good manufacturing practice according to Leon Lachman
Helpful contains for al pharmacy students like diploma, degree and also masters of pharmacy students
So use the contains and build your knowledge.
Manufacturing Control Systems. J R Controls provides control systems for the manufacturing industry. A typical control system will monitor the progress of parts through the manufacturing and finishing process.
Introduction to manufacturing operations, Sanitation, Cross-contamination, Packaging, IPQC, time limitation, Expiration,Calculation of Yield, Production record review, process deviation
Objective and policies of CGMP and Inventory control . This topic is from M.PHARM 1 st year syllabus from modern pharmaceutics
Objective and policies of CGMP
ABBREVIATED NEW DRUG APPLICATION (ANDA),INVESTICATION OF MEDICINAL PRODUCTS D...GOKULAKRISHNAN S
Introduction to ANDA
Regulations applied to ANDA process
Format and content of ANDA
ANDA approval process
Exclusivity
Hatch-Waxman amendments & 180 days exclusivity
Introduction to IMPD
Contents of IMPD
Introduction to IB
Contents of IB
Introduction
Brief description of the drug and the therapeutic class to which it belongs
Chemical and pharmaceutical information
Animal Pharmacolog
Animal Toxicology
Human/Clinical Pharmacology phase I
Therapeutic exploratory trials (Phase II)
Therapeutic confirmatory trials (Phase III)
Special Studies Geriatrics, pediatrics, pregnant or nursing women
Regulatory status in other countries
Prescribing information
Samples and Testing Protocol/s
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Bills have a main role in point of sale procedure. It will help to track sales, handling payments and giving receipts to customers. Bill splitting also has an important role in POS. For example, If some friends come together for dinner and if they want to divide the bill then it is possible by POS bill splitting. This slide will show how to split bills in odoo 17 POS.
Ethnobotany and Ethnopharmacology:
Ethnobotany in herbal drug evaluation,
Impact of Ethnobotany in traditional medicine,
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Bio-prospecting tools for drug discovery,
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Reverse Pharmacology.
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For more information, visit-www.vavaclasses.com
2024.06.01 Introducing a competency framework for languag learning materials ...Sandy Millin
http://sandymillin.wordpress.com/iateflwebinar2024
Published classroom materials form the basis of syllabuses, drive teacher professional development, and have a potentially huge influence on learners, teachers and education systems. All teachers also create their own materials, whether a few sentences on a blackboard, a highly-structured fully-realised online course, or anything in between. Despite this, the knowledge and skills needed to create effective language learning materials are rarely part of teacher training, and are mostly learnt by trial and error.
Knowledge and skills frameworks, generally called competency frameworks, for ELT teachers, trainers and managers have existed for a few years now. However, until I created one for my MA dissertation, there wasn’t one drawing together what we need to know and do to be able to effectively produce language learning materials.
This webinar will introduce you to my framework, highlighting the key competencies I identified from my research. It will also show how anybody involved in language teaching (any language, not just English!), teacher training, managing schools or developing language learning materials can benefit from using the framework.
The French Revolution, which began in 1789, was a period of radical social and political upheaval in France. It marked the decline of absolute monarchies, the rise of secular and democratic republics, and the eventual rise of Napoleon Bonaparte. This revolutionary period is crucial in understanding the transition from feudalism to modernity in Europe.
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1. S.GOKULAKRISHNAN
M.Pharm (Pharmaceutics) – I Year,
Mother Theresa Post Graduate and Research Institute of
Health Sciences,
(A Government of Puducherry Institution)
Puducherry.
cGMP&INDUSTRIAL
MANAGEMENT
GOKULAKRISHNAN cGMP 1
2. Contents
Objectives of CGMP
Layout of buildings, services, equipments &
maintenance
Production organization
material management
handling and transportation
inventory management &control
Production and planning control
Sales forcasting
Budget and cost control
Industrial and personnel relationship
Total quality management
2GOKULAKRISHNAN cGMP
3. CGMP
CGMP refers to Current Good
Manufacturing Practice (CGMP) regulations
enforced by US FDA.
Current Good Manufacturing Practices are the
methods to be used in, the facilities or controls
to be used for, the manufacturing, processing,
packaging or holding of a drug to assure that
such drug meets the requirements of the act,
and has the identity and strength and meets the
quality and purity characteristics that is
represented to possess. 3GOKULAKRISHNAN cGMP
4. Objectives
Ensure that products are consistently manufactured and
controlled to the specified quality.
Concerned with all aspects of production and quality control.
In the manufacture of cosmetic products, overall control and
monitoring
Ensure that the consumer receives products of specified
quality.
The quality of a product depends on the starting
materials, production and quality control processes,
building, equipment and personnel involved.
CGMP regulations assures the identity, strength, quality and
purity of drug products
4GOKULAKRISHNAN cGMP
6. Plant Layout
Plant layout is a coordinated effort to
achieve the final objective to integrate
machines, materials, and personnel for
economic production.
Involves location of different
departments and arrangement of
machinery in each department.
6GOKULAKRISHNAN cGMP
7. TYPES OF PLANT LAYOUT
Process layout or functional layout
Product or straight line layout
Process layout or functional layout
Arrangement of machines of a particular class
doing a particular process as separate department
Advantage
More effective supervision
Division of labour can be provided
Disadvantage
May not be possible as a number of unit operations
have to be performed
7GOKULAKRISHNAN cGMP
8. Product or straight line layout
• The arrangement of machines doing
various operations in a line as one
department
Advantages
Processing of work is quick and smooth
Cost of handling is reduced using conveyers
Manufacturing time can be reduced
Floor space can be properly utilized
8GOKULAKRISHNAN cGMP
9. FACTORS INFLUENCING PLANT
LAYOUT
Basic managerial policies and decisions
Nature of plant location
Type of industry and process
Intermittent industries
Continuous industries
Types of methods of production
Job production
Batch or lot production
Continuous or mass production
9GOKULAKRISHNAN cGMP
10. STORES- LAYOUT
Should be planned in the objectives of:
– Achieving minimum wastage of space
– Achieving maximum ease of operations
The layouts should:
Make optimum utilization of floor space and height
Should be 1.5- 3m wide to facilitate traffic
Permit effective and orderly segregation of various
categories of materials and allow raotation of stock (1st
in 1st out)
Should be ventilated
Have provisions for storage as per specific conditions
Adequately protected from waste, damge and
deterioration.
10GOKULAKRISHNAN cGMP
12. Lighting.
Adequate lighting shall be provided in all areas.
Ventilation, air filtration, air heating and cooling.
Adequate ventilation shall be provided.
Equipment for adequate control over air pressure, micro-
organisms, dust, humidity, and temperature shall be provided
appropriate for the manufacture, processing, packing, or
holding of a drug product.
Air filtration systems, including prefilters and particulate
matter air filters, shall be used appropriate on air supplies to
production areas.
12GOKULAKRISHNAN cGMP
13. Plumbing
Potable Water shall be supplied under continuous positive
pressure in a plumbing system free of defects that could
contribute contamination to any drug product. Potable water
shall meet the standards as prescribed.
Sewage and refuse
Sewage, trash, and other refuse from the building and premises
shall be disposed of in a safe and sanitary manner.
Washing and toilet facilities
Adequate washing facilities shall be provided, including hot
and cold water, soap or detergent, air driers or single-service
towels, and clean toilet facilities easily accessible to working
areas.
13GOKULAKRISHNAN cGMP
14. Sanitation.
Any building used in the manufacture, processing, packing, or
holding of a drug product shall be maintained in a clean and
sanitary condition, Any such building shall be free of
infestation by rodents, birds, insects, and other vermin (other
than laboratory animals). Trash and organic waste matter shall
be held and disposed of in a timely and sanitary manner.
Sanitation procedures shall apply to work performed by
contractors or temporary employees as well as work performed
by full-time employees during the ordinary course of
operations.
14GOKULAKRISHNAN cGMP
16. Equipment should be designed and located to
suit the production of the product.
Design and Construction
The equipment surfaces coming into contact with any
in-process material should not react with or adsorb
the materials being processed.
Equipment should not adversely affect the product
through leaking valves, lubricant drips and through
inappropriate modifications or adaptations.
Equipment should be easily cleaned.
Equipment used for flammable substances should be
explosion proof
16GOKULAKRISHNAN cGMP
17. Installation and Location
Equipment should be located to avoid congestion and
should be properly identified to assure that products do
not become admixed or confused with one another.
Water, steam and pressure or vacuum lines, where
applicable, should be installed so as to be easily
accessible during all phases of operation. They should
be clearly identified.
Support systems such as heating, ventilation, air
conditioning, water (such as potable, purified,
distilled), steam, compressed air and gases (example
nitrogen) should function as designed and identifiable.
17GOKULAKRISHNAN cGMP
18. Equipment cleaning and maintenance
Equipment and utensils shall be cleaned, maintained,
and sanitized at appropriate intervals to prevent
malfunctions or contamination that would alter the
safety, identity, strength, quality, or purity of the drug
product
Written procedures shall be established and followed
for cleaning and maintenance of equipment, including
utensils, used in the manufacture, processing,
packing, or holding of a drug product.
18GOKULAKRISHNAN cGMP
20. Introduction
Definition :- It is an organizational concept which has
the authority & responsibility of all activities,
principally concerned with the flow of materials in
the organization.
Material management works continuously with
production, marketing, sales & quality control.
It has the responsibility of determining the amount of
inventory & its accountability.
It is concerned with planning, directing & controlling
the kind, amount, location, movement of the various
flows of materials used in & produced by a business
enterprise.
320GOKULAKRISHNAN cGMP
21. Functions of Material management
Material planning & programming.
Simplification, standardization & value analysis.
Inventory control & management.
Purchasing of materials in desired quantities without
delays.
Receiving of incoming materials.
Storage, preservation & administration of materials.
Production planning & scheduling.
Transportation (internal & external) & material
handling.
Disposing of rejects & obsolete materials.
Improving operation efficiency through training. 521GOKULAKRISHNAN cGMP
22. Vendor Customer
Material management
Value analysis,
Inventory control,
Production
planning Purchasing,
Vendor development
& Buying
Material handling
Store - keeping
Recycling or
Disposal
Raw
material
Manufacture
Finished
goods
Functions of Material management
622GOKULAKRISHNAN cGMP
23. Materials – Quality & Quantity
Four factors are considered to be essential…
1. Quality,
2.Quantity,
3.Price
4.Delivery date.
1.Quality :-
It is defined as the suitability of an item to accomplish the intended
purpose.
The best is not necessarily the highest quality.
A quality standard is the description of an acceptable quality of a
particular item.
Size reduction equipment, punches, dies, filling equipment, size
separation equipment etc. should comply with quality specifications.
The quality of the material used has direct relationship with the end use
of the product.
723GOKULAKRISHNAN cGMP
24. 2.Quantity :-
From the inventory point of view, quantity standards are
decided on the following parameters…
- Maximum inventory
- Minimum inventory
- Standard order
- Reorder point.
The quantity is mainly based on the calculation of
Economic order quantity (EOQ).
3.The prices of materials are negotiated with the firms
based on certain procedures.
4.Delivery dates are finalized based on the needs of
organization.
824GOKULAKRISHNAN cGMP
25. Value analysis
It is a systematic study of every element for its cost in a part, material or
service to make certain that it performs its function at the lowest possible
cost.
Benefits of Value analysis :-
Cost of existing product or services decreases.
Unnecessary expenditure can be identified & eliminated in products,
processes or services.
Product value gets improved for new materials & processes.
Greater profits acquired
i.e. higher returns on investment.
925GOKULAKRISHNAN cGMP
26. Types of value :-
User value
Esteem value
Cost value
Exchange value.
Value ratio :-
FUNCTION
TOTAL COST
The value can be improved by the following ways…
Reducing the costs
Improving the function
Achieving both the above.
9
VALUE
26GOKULAKRISHNAN cGMP
27. Value analysis technique:
The value of an item can be improved by…
What must it do?
What else does the item do?
What does it cost?
What else will do the job?
What will be the alternative cost?
o Value analysis – what to buy?
o Purchasing analysis – how to buy?
1127GOKULAKRISHNAN cGMP
28. Purchasing – Centralized & Decentralized
Purchasing is an activity directed towards securing
the materials, supplies, equipment & services
required in the operations of an enterprise.
Functions of Purchasing department :-
Ordering section places orders with the vendors
Service section fallows the progress of the purchase orders, its
shipment by the vendor and its final receipt by the company
Records-section maintains all records of quotation, costs,
purchases.
1228GOKULAKRISHNAN cGMP
29. Types of purchasing :
1.Centralized purchasing :
Advantages :
It is an efficient system
It permits a greater degree of specialization for buying
Bargaining capabilities are better
Procuring becomes uniform & consistent materials are
procured without price differentiation
Duplication of efforts is eliminated
Purchasing procedure & payment of invoices become simple.
1329GOKULAKRISHNAN cGMP
30. 2.Decentralized purchasing:
Advantages :
Purchasing system becomes more flexible & efficient
Procurement is faster
When purchases are made in a local place, it promotes better public
relations
Control over purchases is no longer remote.
Disadvantages :
Quantity of discounts offered is less
It involves duplication of efforts.
1430GOKULAKRISHNAN cGMP
32. INTRODUCTION
DEFINITION:
The „inventory‟ can be defined as stock of
items(includes raw materials, in process goods,
finished goods, packaging, & other spares ) in order to
meet an unexpected demand / distribution in the future.
(OR)
Inventory is defined as an itemized list of goods with
their estimated worth, specifically , annual account of
stock taken in any business.
32GOKULAKRISHNAN cGMP
33. Category
PRODUCTION INVENTORY
Special items manufactured to company specification.
MRO INVENTORY
Maintenance, repair & operating supplies which is
consumed in production process.
Do not become part of the product.
IN-PROCESS INVENTORY
Semi finished products found at various stages in the
production operation.
FINISHED GOODS INVENTORY
Complete product ready for shipment. 33GOKULAKRISHNAN cGMP
34. OBJECTIVES
To reduce dependence of one another
To enable each organisation schedule its operation
independently of another.
To reduce material handling costs.
To obtain a reasonable utilization of people &
equipment.
Maximize customer service
Longer production runs
Flexibility in production scheduling.
To avoid stock out and shortage.
34GOKULAKRISHNAN cGMP
35. Benefits
Inventory control ensures an adequate supply of
material & stores , minimizes stock out & shortage &
avoid costly interruption .
It keeps down the investment in inventory.
Eliminate duplication in ordering / replenishing
stocks.
better utilization of available stocks by facilitating
inter –dept transfer within a company
Serves as means for the location and disposition of
inactive & obsolete item of services.
provide a consistent and reliable basis for preparing
financial statement. 35GOKULAKRISHNAN cGMP
36. INVENTORY COSTS
Cost factors must be considered while taking any
decision regarding inventories.
Includes ordering costs , carrying cost, out of
stock/shortage cost and set up cost.
1.ORDERING COST:
Costs of placing an order with a vendor of material
such as preparing a purchase order(receiving and
ordering calls), processing payments(typing costs),
transportation, receiving & inspecting the material.
This cost does not depend on or vary on the number
ordered.
36GOKULAKRISHNAN cGMP
37. 2 .CARRYING COSTS/HOLDING COSTS:
Costs connected directly with material such as
deterioration, pilferage, storage facilities, obsolescence.
Financial costs includes taxes, insurance ,handling
charges & interest
3.OUT OF STOCK/SHORTAGE COST:
Back ordering
Lost sales
Customers goodwill
4.COST OF ITEM:
Direct cost of item
5. SET UP COST:
It include production charge- equipment change over,
report preparation etc. 37GOKULAKRISHNAN cGMP
38. ROLE OF PHARMACIST IN DRUG
PROCUREMENT
The hospital pharmacist should be in collaboration
with the purchase officer, assuming the following
duties:
Maintaining a list of names, addresses, and telephone
numbers of drug manufacturers,wholesalers and local
representatives.
Preparing detailed specifications for drugs, chemicals,
and biologicals.
Preparing request for purchase form.
Preparing receipt memo, if the drugs are received
directly by the pharmacy.
Preparing return goods memo whenever applicable.
38GOKULAKRISHNAN cGMP
39. TECHNIQUES IN INVENTORY
MANAGEMENT
ABC Analysis
VED Analysis
EOQ Analysis
Perpetual Inventory System
Lead time
Buffer Stock
39GOKULAKRISHNAN cGMP
40. ABC ANALYSIS
Always Better Control
It is an inventory categorization method used
for the analysis of range of items that have
different levels of significance and should be
controlled differently.
As per the analysis, the inventories is grouped
into 3 categories based on cost of the material
and money value of consumptions
40GOKULAKRISHNAN cGMP
41. A ITEMS B ITEMS C ITEMS
10 % of total inventories 20 % of total inventories 70 % of total inventories
Consumes about 70% of
total budget
Consumes about 20% of
total budget
Consumes about 10% of
total budget
Requires very strict
control
Requires moderate
control
Requires low control
Requires low or no
safety stocks
Requires low safety
stocks
Requires high safety
stocks
Needs maximum follow
up
Needs periodic follow
up
Needs maximum close
follow up
Handled by senior
officers
Handled by middle
management
Handled by any official
of management
41GOKULAKRISHNAN cGMP
42. ADVANTAGES:
The investment in inventory can be regulated
and funds can be utilized in best possible
manner.
There is a closer and strict control on those
items which represent a major portion of total
stock value.
It helps in enough safety stock of C categories
of items.
The scientific and selective control helps in
maintainence of high stock turnover rate.
42GOKULAKRISHNAN cGMP
43. VED ANALYSIS
This system is based on utility of the material .
The different brands of the drug formulation is
classified as:
V= VITAL ITEMS
E=ESSENTIAL ITEMS
D=DESIRABLE ITEMS
Vital Items:
They are very useful and important in daily patient
care.
Maximum levels of such drugs should be maintained
always in order to have a continuous supply. 43GOKULAKRISHNAN cGMP
44. Essential items:
These are such items which can affect the pharmacy
services to some extent. They require a lesser stock
level when compared to vital drugs.
Essential items are those items whose stock – out cost
is very high for the company.
Desirable items:
These are required by the pharmacy but they donot
effect the quality of service to the patient.
Desirable items are those items whose stock-out or
shortage causes only a minor disruption for a short
duration in the production schedule.
44GOKULAKRISHNAN cGMP
45. EOQ ANALYSIS
EOQ is the quantity of materials to be ordered at one time,
which minimizes the cost.
The correct quantity to buy is the quantity at which the
ordering cost and inventory cost is minimum.
EOQ = √2AB
C
A- annual requirement
B- ordering cost
C- carrying cost
45GOKULAKRISHNAN cGMP
46. PERPETUAL INVENTORY
SYSTEM
The method of recording the store balance after every receipt
and issue to facilitate regular checking and to prevent closing
down for stock taking.
It comprises of :
1.BIN CARD
2.STORE LEDGER
3.CONTINUOUS STOCK TAKING
i. BIN CARD:
Is a document maintained by the store keeper in his store .
It serves the purpose of ready reference.
46GOKULAKRISHNAN cGMP
47. It shows quantity of each material received, issued and
in stock.
ii. STORE LEDGER:
It is kept in the accounting department.
Generally maintained in form of loose leaf cards, so
that they can be easily removed and inserted.
iii. CONTINUOUS STOCK TAKING:
Only a limited no. of items are verified on a day.
Selection of the item should be such that each item
gets checked at least a certain no. of times in a year,
and checking is evenly distributed during the period.
47GOKULAKRISHNAN cGMP
48. LEAD TIME
It is the time taken between the placing of
order and receipt of drugs to the department.
The longer the lead time, longer the safety
stock, resulting in excess of investment in
inventory
48GOKULAKRISHNAN cGMP
49. BUFFER STOCK
Is used in emergency to meet the unseen demands
,i.e, the minimum quantity of particular item which
must be kept in the stock at all the time.
Buffer stock needs the following factors to be taken
into consideration like:
- lead time
- nature of items, rate of consumption
- availability of substance
- re-order level
- stock out cost
49GOKULAKRISHNAN cGMP
50. REFERENCES
FDA “Guidance for Industry: Q7A Good
Manufacturing Practice.
Guidance for Active Pharmaceutical Ingredients,”
Section 19.
ICH Q7 Good Manufacturing Practice Guide For
Active Pharmaceutical Ingredients. Current step 4
version; November 2000 Website. Available from:
http://www.ich.org/LOB/media/MEDIA433.pdf
[Last cited on 2010 Jan 1].
50GOKULAKRISHNAN cGMP