PRP are steps or procedures including GMP & SSOP that control conditions within a food establishment to promote safe food production. They establish basic hygienic requirements including facility location and construction, equipment cleaning, utilities like water and air, cleaning and sanitation programs, personal hygiene facilities, and more. Requirements include proper drainage, separation of raw and processed areas, smooth cleanable surfaces, pest control, and documented cleaning procedures.
Current Good Manufacturing Practices in Food IndustryPECB
Good manufacturing practice (GMP) is a system for ensuring that products are consistently produced and controlled according to the quality standards. There are many risks: unexpected contamination of products, causing damage to health or even death; incorrect labels on container, etc. This webinar will guide you through all of the requirements, steps you need to take going from concepts to implementation of appropriate measures.
Main points covered:
• Current good manufacturing practice (CGMP) requirements
• A Quality Management System for medical devices Required By FDA (Food & Drug Association) USA
• From Concepts to implementation
Presenter:
This webinar was presented by PECB Certified Trainer, who is also a senior consultant, trainer and coach in Occupational Health and Safety, Mr. Raza Shah.
Link of the recorded session published on YouTube: https://youtu.be/9ZTtnAQn3HQ
All organizations recognize the increasing need to demonstrate and provide adequate evidence of their ability to identify and control food safety hazards and the many conditions impacting food safety.
Therefore, ISO 22000 requires that all hazards that may be reasonably expected to occur identified and assessed, resulting in a clear determination of those to be controlled within the organization and those that are to be controlled within the food chain.
Current Good Manufacturing Practices in Food IndustryPECB
Good manufacturing practice (GMP) is a system for ensuring that products are consistently produced and controlled according to the quality standards. There are many risks: unexpected contamination of products, causing damage to health or even death; incorrect labels on container, etc. This webinar will guide you through all of the requirements, steps you need to take going from concepts to implementation of appropriate measures.
Main points covered:
• Current good manufacturing practice (CGMP) requirements
• A Quality Management System for medical devices Required By FDA (Food & Drug Association) USA
• From Concepts to implementation
Presenter:
This webinar was presented by PECB Certified Trainer, who is also a senior consultant, trainer and coach in Occupational Health and Safety, Mr. Raza Shah.
Link of the recorded session published on YouTube: https://youtu.be/9ZTtnAQn3HQ
All organizations recognize the increasing need to demonstrate and provide adequate evidence of their ability to identify and control food safety hazards and the many conditions impacting food safety.
Therefore, ISO 22000 requires that all hazards that may be reasonably expected to occur identified and assessed, resulting in a clear determination of those to be controlled within the organization and those that are to be controlled within the food chain.
this presentation contains information about HACCP implementation in food industry. with example, easy to understand comment below how is this presentation
FSSC 22000 V4.1, USFDA FSMA, SQF V8.0 standards now require to address the controls over food fraud & food defense through vulnerability & threat assessment. Our expert will train your team on the requirements & assist in documenting the plan for VACCP & TACCP.
Global Manager Group provides ISO 22000 awareness and auditor training presentation to learn requirements of revised ISO 22000:2018 standard. It helps corporate professional to establish good food safety management system in organization.
For more information visit: https://www.globalmanagergroup.com/
What is HACCP? (Hazards Analysis Critical Control Point). This presentation provides a basic understanding of HACCP plus a history of its beginnings and how it became adopted by the food international food industry.
Premises’ refers to the buildings and facilities where pharmaceutical processing is done. These places must comply with cGMP requirements.
Premises must be located in a site that is of a size suitable to house all the different departments. The nature of manufacturing and testing to be performed, the magnitude of the operation in terms of daily production levels, the number of products that will be processed, and the storage space required for raw material, in-process and finished goods are some of the important factors to be considered when choosing a location. Other factors such as availability of power, water, labor workforce, and closeness to transport hubs may also impact this decision. From the GMP point of view, the most important factor is the climatic condition and hygiene levels in the surroundings. Pharmaceutical premises must ideally be located away from polluting industries as otherwise, it will burden the air handling and water handling systems.
According to Schedule M of the Drugs and Cosmetics Rules, factory buildings must be situated in a place that avoids contamination risk from the external environment (for example from open drains, public lavatory, open sewage lines, or industry that produces gaseous fumes or strong odors or generates smoke, dust or other chemical emissions).
The building used must be designed, constructed, and maintained in a manner that permits drug production under hygienic conditions. It must be suitable for the operations being performed. The layout of the premises must be such that it reduces the risk of errors, and also avoids the buildup of dirt and cross-contamination that may affect drug product quality. Construction and layout of the building must allow for a sequential and logical flow of the production process and movement of personnel and materials. It must also permit regular cleaning, repair, and maintenance work without harming product quality.
The walls, ceilings, and floors of the building must be smooth and crack-free, easy to clean and disinfect. Surfaces must not shed particles; they must be kept smooth and without any open joints where dust can accumulate.
utitlities
The building must be supplied with adequate light, water, power supply, and ventilation and must be fitted with systems to maintain the temperature and humidity of different areas at desired levels. There must be arrangements to protect against the entry of pests, insects, rodents, etc.
The fittings, ducts, pipes, and ventilation points must be designed in such a way that they do not produce difficult-to-clean recesses. Such points must be located to be easily accessible for maintenance work without having to enter the manufacturing areas.
this presentation contains information about HACCP implementation in food industry. with example, easy to understand comment below how is this presentation
FSSC 22000 V4.1, USFDA FSMA, SQF V8.0 standards now require to address the controls over food fraud & food defense through vulnerability & threat assessment. Our expert will train your team on the requirements & assist in documenting the plan for VACCP & TACCP.
Global Manager Group provides ISO 22000 awareness and auditor training presentation to learn requirements of revised ISO 22000:2018 standard. It helps corporate professional to establish good food safety management system in organization.
For more information visit: https://www.globalmanagergroup.com/
What is HACCP? (Hazards Analysis Critical Control Point). This presentation provides a basic understanding of HACCP plus a history of its beginnings and how it became adopted by the food international food industry.
Premises’ refers to the buildings and facilities where pharmaceutical processing is done. These places must comply with cGMP requirements.
Premises must be located in a site that is of a size suitable to house all the different departments. The nature of manufacturing and testing to be performed, the magnitude of the operation in terms of daily production levels, the number of products that will be processed, and the storage space required for raw material, in-process and finished goods are some of the important factors to be considered when choosing a location. Other factors such as availability of power, water, labor workforce, and closeness to transport hubs may also impact this decision. From the GMP point of view, the most important factor is the climatic condition and hygiene levels in the surroundings. Pharmaceutical premises must ideally be located away from polluting industries as otherwise, it will burden the air handling and water handling systems.
According to Schedule M of the Drugs and Cosmetics Rules, factory buildings must be situated in a place that avoids contamination risk from the external environment (for example from open drains, public lavatory, open sewage lines, or industry that produces gaseous fumes or strong odors or generates smoke, dust or other chemical emissions).
The building used must be designed, constructed, and maintained in a manner that permits drug production under hygienic conditions. It must be suitable for the operations being performed. The layout of the premises must be such that it reduces the risk of errors, and also avoids the buildup of dirt and cross-contamination that may affect drug product quality. Construction and layout of the building must allow for a sequential and logical flow of the production process and movement of personnel and materials. It must also permit regular cleaning, repair, and maintenance work without harming product quality.
The walls, ceilings, and floors of the building must be smooth and crack-free, easy to clean and disinfect. Surfaces must not shed particles; they must be kept smooth and without any open joints where dust can accumulate.
utitlities
The building must be supplied with adequate light, water, power supply, and ventilation and must be fitted with systems to maintain the temperature and humidity of different areas at desired levels. There must be arrangements to protect against the entry of pests, insects, rodents, etc.
The fittings, ducts, pipes, and ventilation points must be designed in such a way that they do not produce difficult-to-clean recesses. Such points must be located to be easily accessible for maintenance work without having to enter the manufacturing areas.
Design and Construction of plant as per the GMP Guidelines.pdfMohiniTawade
GMP is that part of Quality assurance which ensures that the products are consistently
manufactured and controlled to the Quality standards appropriate to their intended use
MANUFACTURING OF PARENTRALS
1. Formulation and Raw Materials:
Concept: The process begins with the formulation of the parenteral drug, determining its composition and concentration.
Raw Materials: High-quality pharmaceutical-grade raw materials, including active pharmaceutical ingredients (APIs), excipients, and solvents, are selected based on their compatibility and purity.
2. Sterilization of Raw Materials:
Concept: Due to the sterile nature of parenteral products, all raw materials, including the API and excipients, must undergo rigorous sterilization.
Methods: Common sterilization methods include autoclaving, filtration, and aseptic processing to ensure aseptic conditions throughout the manufacturing process.
3. Manufacturing Process:
Preparation: The formulation is prepared, and various components are weighed and measured precisely.
Mixing: The ingredients are mixed under controlled conditions to achieve a homogeneous blend, ensuring uniform distribution of the API and other components.
Filtration: The solution is then filtered to remove any particulate matter and ensure clarity.
Filling: The sterile drug solution is filled into vials, ampoules, or other suitable containers in a controlled environment, maintaining sterility.
4. Sterilization of Final Product:
Terminal Sterilization: The final product, in its container, undergoes terminal sterilization methods like autoclaving or gamma irradiation to eliminate any microbial contamination that may have occurred during the manufacturing process.
Hygiene standards and procedures usually described as Good Hygienic Practices (GHP) or Good Manufacturing Practices (GMP), have been in place for many years and constituted an essential tool in traditional food control. These concepts are still essential in a modern food control system by providing the basic environmental and operating conditions for production of safe food and thus being a requisite or foundation for HACCP in an overall food safety management program. What is new is the concept of formalizing the prerequisite program alongside HACCP and the legal requirement in some countries (USA) of documented monitoring of certain sanitation areas.
Designing of aseptic area, laminar flow equipment: Study of different source ...Ms. Pooja Bhandare
Designing of aseptic area, laminar flow equipment: Study of different source of contamination in aseptic area and methods of prevention, clean area classification. PHARMACEUTICALMICROBIOLOGY (BP303T)Unit-IVPart-1
Introduction: Designing of Aseptic Area . i) The clean-up area,
ii) The compounding area,
iii) The aseptic area,
iv) The quarantine area and
v) The packaging/labelling area.
Flow diagram of aseptic area. Floors, walls and ceilings, Doors, windows and services Personnel and protective clothing Cleaning and disinfection. Air Supply. Laminar flow equipment. Vertical laminar air flow bench
Horizontal laminar air flow bench
High Efficiency Particulate Air (HEPA) Filter. Operating Instructions Uses of Laminar Air Flow.Advantages of Laminar Air Flow.Limitations of Laminar Air Flow. Air flow pattern Unidirectional airflow
Non-unidirectional airflow
Combined airflow
Different Sources of Contamination in an Aseptic Area
1) Personnel:
2) Buildings and Facilities
3) Equipment and Utensils:
4) Raw Materials
5) Manufacturing Process:
Methods of Prevention of Contamination Clean Area Classification
Ang Chong Yi Navigating Singaporean Flavors: A Journey from Cultural Heritage...Ang Chong Yi
In the heart of Singapore, where tradition meets modernity, He embarks on a culinary adventure that transcends borders. His mission? Ang Chong Yi Exploring the Cultural Heritage and Identity in Singaporean Cuisine. To explore the rich tapestry of flavours that define Singaporean cuisine while embracing innovative plant-based approaches. Join us as we follow his footsteps through bustling markets, hidden hawker stalls, and vibrant street corners.
At Taste Of Middle East, we believe that food is not just about satisfying hunger, it's about experiencing different cultures and traditions. Our restaurant concept is based on selecting famous dishes from Iran, Turkey, Afghanistan, and other Arabic countries to give our customers an authentic taste of the Middle East
Piccola Cucina is regarded as the best restaurant in Brooklyn and as the best Italian restaurant in NYC. We offer authentic Italian cuisine with a Sicilian touch that elevates the entire fine dining experience. We’re the first result when someone searches for where to eat in Brooklyn or the best restaurant near me.
Roti Bank Hyderabad: A Beacon of Hope and NourishmentRoti Bank
One of the top cities of India, Hyderabad is the capital of Telangana and home to some of the biggest companies. But the other aspect of the city is a huge chunk of population that is even deprived of the food and shelter. There are many people in Hyderabad that are not having access to
Key Features of The Italian Restaurants.pdfmenafilo317
Filomena, a renowned Italian restaurant, is renowned for its authentic cuisine, warm environment, and exceptional service. Recognized for its homemade pasta, traditional dishes, and extensive wine selection, we provide a true taste of Italy. Its commitment to quality ingredients and classic recipes has made it a adored dining destination for Italian food enthusiasts.
Food and beverage service Restaurant Services notes V1.pptx
Prerequisite Program (PRP).pptx
1. Prerequisite Program (PRP):
• Prerequisite Programs:
PRP are steps or procedures including GMP & SSOP, which control the operational conditions within
a food establishment and promote environmental conditions that are favorable for safe food
production/Manufacturing.
These are “Basic Conditions and activities” that are necessary to maintain a hygienic environment
throughout the food chain
The Food safety Team establishes PRPs
For FSSC 22000 will also include prerequisite programs to meet the requirements of ISO/TS
22002-1 or ISO/TS 22002-4
2. Requirement of ISO 22002-1 & PAS 220
• Location Surrounding of facility:
• Building Design, Construction & Layout of Premises
• Equipment: Cleaning & Maintenance
• Utilities: Air/Water/Energy
• Cleaning & Sanitation of premises
• Personal Hygiene & Employee facilities
• Raw material procurement
• Pest Control
• Product Information
• Storage
• Rework
• Waste disposal
• Product recall procedure
• Food Defense (VACCP/TACCP)
3. • Location & Construction of Facility:
i. Facility shall be situated away from environmentally polluted areas like open sewage, drain,
public lavatory or any factory which produces disagreeable or obnoxious odour, fumes,
excessive soot, dust, smoke, chemical or biological emissions to avoid risk of contamination
from external environment. In case it is already existing, appropriate control measures shall be
taken.
ii. The site boundaries shall be clearly identified with appropriate access control to prevent the
chances of theft and sabotage. Dogs, cats or other pet animals should not be allowed to enter
the premises.
iii. The manufacturing premise shall not have direct access to any residential area.
iv. The manufacturing premises shall be located away from flood prone area. Where the premises
are located in areas prone to flooding, it is recommended that height of the manufacturing area
should be suitably elevated to prevent the risks due to flooding.
v. The surrounding areas of the establishment shall be kept in good order. Roads, yards, parking
lots outside the factory building should be free of debris and refuse, and from any source of
pollution.
vi. There should not be any stagnant water surrounding the facility. Where buildings are
surrounded by grassed or planted areas, a clear space should be provided between the grassed
planted areas and the building. Such grassed/planted areas should be regularly tended and
maintained
4. • Building Design, Construction & Layout of Premises:
i. Plant layout should be designed, constructed and maintained in order to facilitate good manufacturing
and hygienic practices.
ii. The building shall provide adequate working space with a logical flow of materials, products, personnel
and to the extent that is practicable physical separation of raw from processed area to prevent any
cross-contamination.
iii. Entry to the manufacturing area shall be through a double door airlock facility
iv. Sufficient space and proper placement of equipment’s as is necessary for the maintenance of sanitary
operations.
v. The premises should have a proper space for inward and outward vehicle movement. Openings
intending for transfer of materials shall be designed to minimize any cross contamination from foreign
matter, pests, etc. have adequate controls to Designed, constructed and maintained to prevent entry of
insects and rodents.
vi. Walls and Partitions shall be soundly constructed of materials that are durable, cleanable, and
impervious to food, grease and water with no toxic effect in product. For example: emulsion oil paint
(which is easily cleanable by wiping); tiles(which are less porous and causes less crevices)., Premises
shall be free of flaking paint and plaster to prevent the accumulation of dust, minimize condensation,
and shredding of particles; Wall floor joints should be curved in processing and packaging areas to
facilitate cleaning; Wall and pillar guards (SS) should be used to avoid daily wear and tear of the
surfaces.
vii. Ceilings- Shall be maintained in sound condition and constructed of materials that are durable,
cleanable, and impervious to food, grease and water with no toxic effect in intended use; Shall prevent
the entry of dirt, dust and pests; Shall be free from flaking paint or plaster. Overhead fixtures Shall be
suitably protected so that they do not act as contaminants in case of breakage.
5. • Building Design, Construction & Layout of Premises:
viii. Floors shall be non-slippery, sloped appropriately, to allow adequate drainage, The drainage shall
flow opposite to the flow of manufacturing process flow; It should be maintained in good repair
with no cracks and crevices and made of materials that are durable and easy to clean such as Epoxy
coated floors or PU flooring or any other suitable flooring. The floor and the walls should not be
damp or moist.
ix. Doors& Window’s shall have smooth, non-absorbent surfaces, Wooden doors are not
recommended as it promotes mould growth, termites with ageing, shall be easy to clean, close-
fitting and with suitable precautions to prevent entry of pests, Gaps if any between the door and
the floor should be closed with suitable material like rubber strips, polyurethane etc. to avoid pest
entry, To ensure dust, insects, birds and animals to be kept out of the premises entry/exit points
should be suitably protected with such as PVC strip /air curtains/ doors with automatic self-closing
devices etc. For External opening windows, roof vents or exhaust fan, where present, shall be
adequately screened to avoid any external pest ingress. Stairs, lift cages and auxiliary structures
such as platforms, ladders, chutes should be so situated and constructed as not to cause
contamination to product. They should also be well maintained.
6. • Equipment: Cleaning & Maintenance:
i. Equipment and containers that come in direct contact with food (including food contact surfaces)
and used for food handling, storage, processing, packing shall be: -
• located, designed and fabricated so that it permits necessary maintenance and periodic cleaning.
• kept in good order, repair and condition as to minimize any risk of contamination. These include free from
cracks, crevices, open seams etc.
• Made of impervious, corrosion free material (Stainless Steel) which do not impart any toxicity to the food
material and shall be easy to clean.
• Shall be placed to achieve easy and effective cleaning of adjacent areas like floors, walls, ceilings and other
surfaces.
ii. Equipment, containers and piping should be clearly labelled and identifiable.
iii. All openings such as manholes, inlets, outlets, draining out of points, etc. should be made such
that they can be locked and/or effectively sealed.
iv. Manufacturing vessels, pipework, and material handling equipment are well bonded and smooth
to prevent material build up and promote sanitary conditions.
v. Hygienic design features may include:
• Pipes shall be sloped, with no dead-legs or right-angled bends,
• Domed tops, curved sides, conical bases for vessels/tanks.
• Flexible hoses shall have a smooth (not ribbed) internal surface and have fittings which are sanitary and easy
to connect/disconnect hoppers.
7. • Equipment: Cleaning & Maintenance:
vi. All utensils/ container containing food products shall be covered with a properly fitted cover/lid or
with a clean gauze net/ any other material. This helps to completely protect food from dust, dirt,
flies and other insects.
vii. There shall be appropriate facilities for cleaning and disinfecting the food contact equipment and
instruments, and wherever possible Clean-In-Place (CIP) should be adopted.
viii. Defective equipment shall be removed from production and quality control areas. If the equipment
is such that they cannot be removed, they should be clearly indicated with their status as (NOT IN
USE/ UNDER MAINTENANCE).
8. • Utilities: Water/Air/Energy:
i. Water System-
• Adequate supply of potable water shall be available to meet operational needs.
• Water including steam/Ice used as a product ingredient or in contact with food of food contact surfaces
or used for equipment and plant cleaning shall be potable.
• Potable water quality shall be as specified in the latest edition of BIS standard on drinking water (IS
10500). Potable water shall be analyzed at least semi-annually to confirm that it meets the
requirements of this standard.
• Where it is necessary to store water, storage facilities including the storage tanks and water pipes shall
be adequately designed, made of material that is non-toxic, corrosion resistant material and periodic
cleaned and maintained to prevent contamination and records of the same should be maintained. The
tanks shall be covered to prevent access by animals, birds, pests and other extraneous matter.
• Where water filters are used, they shall be regularly monitored & effectively maintained.
• Recycled water used in processing or as an ingredient shall not present risk of contamination. It shall be
of the same standard as potable water.
• Non potable water (for use in, for example, steam production, firefighting& refrigeration equipment
and other similar purposes where it will not contaminate food) shall have a separate system. Non-
potable water systems shall be identified and shall not connect with, or allow reflux into, potable water
systems.
• The material of construction of pumps, valves, storage and distribution skids shall be non-reactive, non-
corrosive, non-leaching and sanitary in design.
• Water lines (used in internal Cleaning & as ingredients) shall be clearly separated and identified from
others. Color coding of separate pipelines for potable water and non-potable water is recommended.
9. • Utilities: Water/ Air/Energy:
ii. Air Quality & Environmental condition:
• Air quality and environment conditions shall be maintain as recommended for various areas – Most
likely -ISO 8 with RLAF ISO 5, Temperature should not be more than 25° C and Relative Humidity (RH)
should not be more than 60%+/- 5% or as recommended.
• The air shall not flow from contaminated to clean areas, the ventilation systems shall be so designed.
• Adequate Differential Pressure shall be maintained between different classified areas. Systems shall be
accessible for cleaning, filter changing and maintenance. Recommended differential pressure in
adjacent areas should be min 0.5 mm of Water Column (5-10 psi).
• Air filters, exhaust and air intake ports shall be examined periodically for physical filter integrity.
• Periodic air quality monitoring shall be in place.
• Ventilation systems, natural and/or mechanical, including Heating, Ventilation and Air Conditioning
(HVAC) systems or air-conditioning, air filters, exhaust fans, wherever required, shall be designed and
constructed so that pre-decided conditions are maintained
iii. Compressed air and other gases:
• Compressed air & other gas used in manufacturing shall be maintained so as to prevent contamination.
• Compressed air / gases intended for direct or incidental product contact shall be from a source
approved for food contact use, filtered to remove dust, oil and water to ensure microbial quality and so
shall be checked at least in a year.
• It is recommended to have an oil free Compressed air system.
10. • Utilities: Water/Air/Energy:
iv. Lighting:
• Adequate natural or artificial lighting shall be provided to enable the personnel to operate in a hygienic
manner. Where necessary, lighting should not be such that the resulting colour is misleading.
• The intensity (that is, the lux level) should be adequate to the nature of the operation. Recommended
lux level for processing areas) is at least 540 LUX, as per USFDA Food Code 2013.
• Light fixtures shall be protected to ensure that materials, product or equipment are not contaminated
in the case of breakages.
11. • Cleaning & Sanitation of premises:
i. Cleaning & Sanitation:
• Effective cleaning of premises and equipment must be carried out at the defined frequency and using the
methods and materials specified in well-designed cleaning schedules and procedures.
• Cleaning standard operating procedures (SOPs) shall be defined and records demonstrating compliance shall
be maintained.
• Premises should be regularly inspected for cleanliness and good housekeeping.
• Cleaning materials should be stored in a separate location in order to avoid contamination
• Cleaning and sanitizing programs shall be established at facility to ensure that the food-processing equipment and
environment are maintained in a hygienic condition to prevent contamination of food, such as from metal shards,
flaking plaster, food debris and chemicals and records of the same shall be maintained. The programme should
ensure that all parts of the establishment are appropriately clean, and shall include the cleaning of cleaning
equipment.
• Master sanitation schedule shall be maintained for overall facility through checklists which includes: -
-Areas, items of equipment and utensils to be cleaned;
- Responsibility for particular tasks;
- Cleaning method and frequency of cleaning; and
- Monitoring arrangements for checking effectiveness of cleaning –
- Person responsible for cleaning
- Persons responsible for monitoring & verification of effectiveness of cleaning
- In case of any deviation what correction & corrective actions being taken.
- Where ever chances of microbial risk with product air count & swab test being recommended.
12. • Cleaning & Sanitation of premises:
i. Cleaning & Sanitation:
• Cleaning and disinfection chemicals shall be food grade wherever chances of it may come in direct or indirect
contact through equipment’s or plant surfaces, handled and used carefully and in accordance with
manufacturers’ instructions, for example, using the correct dilutions, and stored, where necessary, separated
from food, in clearly identified containers to avoid the risk of contaminating food.
• Cleaning shall remove food residues and dirt and it can be carried out by the separate or the combined use of
physical methods, such as heat, scrubbing, turbulent flow and vacuum cleaning or other methods that avoid the
use of water, and chemical methods using appropriate cleaning agents.
• These facilities should be constructed of corrosion resistant materials, be easy to clean and shall have adequate
supply of hot and cold potable water, where appropriate. It is recommended to have different colour for hot and
cold pipes.
• A validation mechanism should be in place for all cleaning program.
• Cleaning procedure should generally involve-
- Removing gross visible debris from surfaces.
- Applying a detergent solution to loosen soil and bacterial film (cleaning)
- Rinsing with water (hot water where possible) to remove loosened soil and residues of detergent.
- Dry cleaning or other appropriate methods for removing and collecting residues and debris and
- Where necessary, cleaning should be followed by disinfection with subsequent rinsing.
• Designated area with lock & key provision should be allocated for cleaning equipment’s & chemicals.
• Where ever necessary & applicable CIP procedure should be defined for equipment’s cleaning.
13. • Cleaning & Sanitation of premises:
ii. House keeping:
• A housekeeping schedule covering manufacturing and storage areas shall be maintained.
• The surrounding areas including roads, parking lots and drains should be well maintained.
• Walls and floors should be maintained neat and clean. Ceilings and light fixtures should be easy to clean.
• Drains should be sufficiently sized and well sloped. Drains should have removable grates installed for ease of
cleaning.
• For 3rd party (contract) cleaning companies, the supplier should define clear scope, details of services and
responsibilities.
• Waste storage areas should be clearly marked and waste shall be disposed of in a timely manner.
14. • Personal Hygiene & Employee facilities:
• Personnel hygiene facilities shall be available to ensure that an appropriate degree of personal hygiene can
be maintained to avoid any cross contamination. Such facilities shall be suitably located & designated.
• Facility shall have following facilities-.
i. Hand washing facilities:
• Facility with shot and cold or suitable temperature controlled potable water with suitable hygienic means of drying hands
can be provided in such a position that the employee must pass them when entering the processing areas. This will help
employees to automatically get an alert for hand washing without a miss.
• Where hot and cold water are available, mixing taps should be provided.
• Hand washing notices shall be posted on walls near hand wash stations.
• Non- Perfumed liquid soap should be used in dispensers to wash hands as soap bars are a potential source of cross
contamination.
• The design of taps should be such that there is no hand contact after washing while closing the taps. Preferably, Automatic,
elbow or foot operated taps are used in food manufacturing units
ii. Hand drying and sanitizing facility:
• Hand drier where installed should be in working condition at all the times during working hours.
• Where paper towels are used, a sufficient number of dispensers and receptacles should be provided near to each washing
facility. Paper towel rolls should be covered from top at all time to avoid dust and dirt on them.
• Generally, and preferably, hand driers are considered better than paper towels based on cost efficiency and effectiveness.
• The dustbins used to throw the used-paper towels, should be foot-operated. This avoids any direct hand contact (washed
hands) to open the dustbin.
• Self-drying hand sanitizer should be provided and should be used after drying of hands. This is the next step of disinfecting
hands after cleaning.
15. • Personal Hygiene & Employee facilities:
iii. Lavatories:
• Lavatories shall be separate from other areas and shall not be directly connected to the production or storage areas.
• Sufficient number and separate toilets/urinals for male and female should be provided. Industry best practice of 1:25 is
followed for facility: employee ratio.
• Adequate supply of water should be provided in toilets and urinals. Potable water should be used at the toilet wash basin
stations, as the employees may need to touch food items while in production areas.
• All toilet facilities should be clean and sanitized at all times of the working hours.
• Toilets should be so designed so as to ensure hygienic removal of waste matter.
• Toilets should be well lit and ventilated and should not open directly into food handling areas
iv. Changing facilities
v. Rest and refreshment room