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JOHN DOE
Licensed Real Estate Salesperson


Tlf.: +11 111 111 111
jhondoe@realestate.com
www.loremipsum.com



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JOHN DOE
Licensed Real Estate Salesperson


Tlf.: +11 111 111 111
jhondoe@realestate.com
www.loremipsum.com



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3R Pharmaceutical Industries is a manufacturing company that was established in 1993 to cater to the growing demands of pharmaceutical companies for toll and contract manufacturing in the MENA region. In 1994 3R was licensed by the JFDA for the production of creams, ointments and cosmetics, and has a complete manufacturing line for that purpose. In 2001 3R was licensed by the JFDA for the secondary packaging of pharmaceutical products. As of 2020, 3R partnered with Advancis Portugal for the secondary packaging of a best selling Supplements and Vitamins product line, and also partnered with JPM (Jordanian Pharmaceutical Manufacturing Co.) in that same year for the toll manufacturing of local Pharma products. Over the years 3R has produced its own brands as well, which include Simona cosmetics, Erasmic shaving creams, Aspitect 81mg (Aspirin) and a newfound Alcohol Gel and Hand Wash product line in light of the Covid 19 pandemic.
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3R Pharmaceutical Industries is a manufacturing company that was established in 1993 to cater to the growing demands of pharmaceutical companies for toll and contract manufacturing in the MENA region. In 1994 3R was licensed by the JFDA for the production of creams, ointments and cosmetics, and has a complete manufacturing line for that purpose. In 2001 3R was licensed by the JFDA for the secondary packaging of pharmaceutical products. As of 2020, 3R partnered with Advancis Portugal for the secondary packaging of a best selling Supplements and Vitamins product line, and also partnered with JPM (Jordanian Pharmaceutical Manufacturing Co.) in that same year for the toll manufacturing of local Pharma products. Over the years 3R has produced its own brands as well, which include Simona cosmetics, Erasmic shaving creams, Aspitect 81mg (Aspirin) and a newfound Alcohol Gel and Hand Wash product line in light of the Covid 19 pandemic.
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About Us
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Mixing Room (1)


This room is specialized for mixing raw materials to produce semi-solid mixtures using a TMP mixer; this includes creams and ointments. The mixing technician receives material for only one batch of a certain product from the waiting room. The technician mixes the weighed raw material according to the manufacturing procedure in the batch record. The process includes calibrating the temperature, speed, and direction of the blade’s movement. Once the process is complete, the mixture is poured into drums allocated for the batch. Identification labels with details of the batch record are placed on each drum.
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Mixing Room (1)


This room is specialized for mixing raw materials to produce semi-solid mixtures using a TMP mixer; this includes creams and ointments. The mixing technician receives material for only one batch of a certain product from the waiting room. The technician mixes the weighed raw material according to the manufacturing procedure in the batch record. The process includes calibrating the temperature, speed, and direction of the blade’s movement. Once the process is complete, the mixture is poured into drums allocated for the batch. Identification labels with details of the batch record are placed on each drum.
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Microbiology lab


The microbiology lab is isolated from the rest of the labs due to the high-risk nature of the tests conducted here. As such, the micro lab technician must be fully dressed in personal protective equipment.


The lab is devoted to analysing the primary products to ensure that they are free from pathogenic microbes. The total microbial count must fall within a certain range according to ISO standards.


To conduct these microbiological tests, several pieces of equipment are used. This includes an autoclave for sterilizing the apparatus; a laminar flow to conduct tests in a controlled environment; and finally, an incubator for growing bacterial and fungi culture to test the efficacy of all medical device and cosmetic products.




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Microbiology lab


The microbiology lab is isolated from the rest of the labs due to the high-risk nature of the tests conducted here. As such, the micro lab technician must be fully dressed in personal protective equipment.


The lab is devoted to analysing the primary products to ensure that they are free from pathogenic microbes. The total microbial count must fall within a certain range according to ISO standards.


To conduct these microbiological tests, several pieces of equipment are used. This includes an autoclave for sterilizing the apparatus; a laminar flow to conduct tests in a controlled environment; and finally, an incubator for growing bacterial and fungi culture to test the efficacy of all medical device and cosmetic products.




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Labeling Room


Once the primary product is complete and filled, the items are then brought here to be branded. Depending on the shape of our products, this process is done with the help of one of our two labelling machines.


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Labeling Room


Once the primary product is complete and filled, the items are then brought here to be branded. Depending on the shape of our products, this process is done with the help of one of our two labelling machines.


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Finished Products Warehouse


It is a ventilated, temperature and humidity-controlled area where finished products are stored in line with Good Manufacturing Practice standards. The finished products are organized in shipping boxes and are clearly labeled with their specifications. The products are organized according to product line and purchase order in preparation for dispatch to distributors.


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Finished Products Warehouse


It is a ventilated, temperature and humidity-controlled area where finished products are stored in line with Good Manufacturing Practice standards. The finished products are organized in shipping boxes and are clearly labeled with their specifications. The products are organized according to product line and purchase order in preparation for dispatch to distributors.


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Posi Fill Machine No. PD-029A


It is specific for filling ointments and creams in jars.
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Posi Fill Machine No. PD-029A


It is specific for filling ointments and creams in jars.
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Filling Room


This room is dedicated for multiple functions which include the filling of ointments, creams, gels, or liquids in either jars, small bottles, or sachets.


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Filling Room


This room is dedicated for multiple functions which include the filling of ointments, creams, gels, or liquids in either jars, small bottles, or sachets.


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Raw Material Warehouse


It is a ventilated, temperature and humidity-controlled area where raw materials are stored in line with Good Manufacturing Practice standards. The raw materials are organized according to type and are clearly labelled with their specification details.


The raw materials admitted to this store have already gone through analysis and have been approved by the Quality Control officer during the quarantine stage.


The raw materials are then incrementally dispatched from the warehouse to the weighing room depending on production demand.



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Raw Material Warehouse


It is a ventilated, temperature and humidity-controlled area where raw materials are stored in line with Good Manufacturing Practice standards. The raw materials are organized according to type and are clearly labelled with their specification details.


The raw materials admitted to this store have already gone through analysis and have been approved by the Quality Control officer during the quarantine stage.


The raw materials are then incrementally dispatched from the warehouse to the weighing room depending on production demand.



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Preparation Area


In this room, the production staff prepares the primary packaging material prior to its transfer to the production area. The primary packaging is removed from the carton boxes and is placed on a steel or plastic tray. This ensures that all products are sterile before entry to the production area.
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Preparation Area


In this room, the production staff prepares the primary packaging material prior to its transfer to the production area. The primary packaging is removed from the carton boxes and is placed on a steel or plastic tray. This ensures that all products are sterile before entry to the production area.
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Packaging Material Receiving Area


This is the area where primary and secondary packaging material from the warehouses enter the production area. The Warehouse Keeper transfers material according to production demand, however, only one batch enters the production area at any given time. The Production Officer, under the supervision of the Quality Assurance Officer, receives the material and records it in the logbook.



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Packaging Material Receiving Area


This is the area where primary and secondary packaging material from the warehouses enter the production area. The Warehouse Keeper transfers material according to production demand, however, only one batch enters the production area at any given time. The Production Officer, under the supervision of the Quality Assurance Officer, receives the material and records it in the logbook.



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Filling Machine No. PD-036


With this machine the technician places the mixture in the hopper while another secures the bottles on the conveyer belt where every four bottles are filled simultaneously. At the end of the belt the machine itself includes a printing mechanism where bottles are printed with the Batch Number, Manufacturing and Expiration Date. Another employee collects the filled and printed bottles to insert the lids and ensure their weight is within range using a weighing scale. Bottles are then placed in plastic bins in preparation for transfer onto the Packaging area.


The filling machine can fill 1,000 bottles per hour.
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Filling Machine No. PD-036


With this machine the technician places the mixture in the hopper while another secures the bottles on the conveyer belt where every four bottles are filled simultaneously. At the end of the belt the machine itself includes a printing mechanism where bottles are printed with the Batch Number, Manufacturing and Expiration Date. Another employee collects the filled and printed bottles to insert the lids and ensure their weight is within range using a weighing scale. Bottles are then placed in plastic bins in preparation for transfer onto the Packaging area.


The filling machine can fill 1,000 bottles per hour.
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Filling Machine No. PD-37


It is specific for filling small bottles (5ml - 150ml) with gel and liquids.
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Filling Machine No. PD-37


It is specific for filling small bottles (5ml - 150ml) with gel and liquids.
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Sachets Machines


It is specific for filling sachets with liquid or gel purposed for sample distribution. Examples include sanitizers, shampoos, lotions, and condiments.
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Sachets Machines


It is specific for filling sachets with liquid or gel purposed for sample distribution. Examples include sanitizers, shampoos, lotions, and condiments.
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Labeling Machine No. PD-38


This machine is used for products with a flat surface. The machine places one label on the front and another on the back. The machine can label up to 1,000 units per hour.
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Labeling Machine No. PD-38


This machine is used for products with a flat surface. The machine places one label on the front and another on the back. The machine can label up to 1,000 units per hour.
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Intermediate Room


This is an intermediate area where the filled tubes are stored until one batch is complete.
Once one batch of filled tubes has been consolidated, they are then transferred onto the secondary packaging area.



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Intermediate Room


This is an intermediate area where the filled tubes are stored until one batch is complete.
Once one batch of filled tubes has been consolidated, they are then transferred onto the secondary packaging area.



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Labeling Machine No. PD-39


This machine is used for sticking labels on items with a round surface. The machine can label up to 900 units per hour.
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Labeling Machine No. PD-39


This machine is used for sticking labels on items with a round surface. The machine can label up to 900 units per hour.
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Melter PD-006


Used for melting the solid materials before they are placed in the TMP Mixer.
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Melter PD-006


Used for melting the solid materials before they are placed in the TMP Mixer.
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Mixer. Capacity


This machine is dedicated to preparing nail polish mixtures and can handle up to 50kg in one mix.
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Mixer. Capacity


This machine is dedicated to preparing nail polish mixtures and can handle up to 50kg in one mix.
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Mixing Room (2)


This room is specialized for mixing raw materials to produce perfumed liquid mixtures including nail polish remover and nail polish.
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Mixing Room (2)


This room is specialized for mixing raw materials to produce perfumed liquid mixtures including nail polish remover and nail polish.
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TMP Mixer No. PD-007A


Used for mixing creams or ointments ingredients weighing 300 kg per batch. One mixture needs 4 hours to be completed and another half hour to be emptied into specific and identified drums.
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TMP Mixer No. PD-007A


Used for mixing creams or ointments ingredients weighing 300 kg per batch. One mixture needs 4 hours to be completed and another half hour to be emptied into specific and identified drums.
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Mixing Room (3)


This room is dedicated for producing liquid mixtures. There are three machines each with a different capacity. Depending on the production demand the relevant mixing machine is utilized.
Examples of mixtures produced in this room include shampoos, rubbing alcohols, colognes, alcohol gels and liquid disinfectant soaps.



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Mixing Room (3)


This room is dedicated for producing liquid mixtures. There are three machines each with a different capacity. Depending on the production demand the relevant mixing machine is utilized.
Examples of mixtures produced in this room include shampoos, rubbing alcohols, colognes, alcohol gels and liquid disinfectant soaps.



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Mascott Mixer No. PD-14A


This machine is dedicated to preparing the mixture of acetone or perfumed liquids. The capacity is 500kg per mixture requiring about 4 hours to complete.
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Mascott Mixer No. PD-14A


This machine is dedicated to preparing the mixture of acetone or perfumed liquids. The capacity is 500kg per mixture requiring about 4 hours to complete.
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Weighing Room


This room is dedicated to weighing the raw materials to prepare the mixtures for production.


Under the supervision of the Quality Assurance Officer, the material is weighed according to the master formula in the batch record. Only one type of raw material is present in the weighing room at any given time.
The weighed raw material is then placed in individual drums or sealed bags and are identified with labels.


The drums and sealed bags are then delivered to the waiting area.



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Weighing Room


This room is dedicated to weighing the raw materials to prepare the mixtures for production.


Under the supervision of the Quality Assurance Officer, the material is weighed according to the master formula in the batch record. Only one type of raw material is present in the weighing room at any given time.
The weighed raw material is then placed in individual drums or sealed bags and are identified with labels.


The drums and sealed bags are then delivered to the waiting area.



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Research and Development Lab


This lab is dedicated for research and development of new products.
The lab technician experiments with different formulas to produce a mockup of the most suitable mixture. The technician then performs and follows up with necessary analysis, evaluation, and documentation of the chosen formula.


Based on regulations, the new formula may require validation and stability studies. The technician then compiles the necessary documents to submit to the regulatory bodies for approval.


The technician is also responsible for the calibration and performance of the lab equipment and stability chambers.



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Research and Development Lab


This lab is dedicated for research and development of new products.


The lab technician experiments with different formulas to produce a mockup of the most suitable mixture. The technician then performs and follows up with necessary analysis, evaluation, and documentation of the chosen formula.


Based on regulations, the new formula may require validation and stability studies. The technician then compiles the necessary documents to submit to the regulatory bodies for approval.


The technician is also responsible for the calibration and performance of the lab equipment and stability chambers.



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Water Filtration System


The water used in any of our mixtures must be purified before it enters the production area. The water is filtered through reverse osmosis as follows:


First the water passes the cartridge which removes chlorine. Second, the water passes through 3 membranes to filter large impurities. The water then passes through another set of 3 membranes to remove the small elements and salt. The last involves the water passing through a UV filter to remove bacteria and fungi.


The resulting water is free of impurities and microbes, has a PH around 7, and electrolytic conductivity less than 10 to align with GMP standards.



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Water Filtration System


The water used in any of our mixtures must be purified before it enters the production area. The water is filtered through reverse osmosis as follows:


First the water passes the cartridge which removes chlorine. Second, the water passes through 3 membranes to filter large impurities. The water then passes through another set of 3 membranes to remove the small elements and salt. The last involves the water passing through a UV filter to remove bacteria and fungi.


The resulting water is free of impurities and microbes, has a PH around 7, and electrolytic conductivity less than 10 to align with GMP standards.



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Tube-Filling Room


After the mixture has cooled down and approval has been granted by the Quality Control Officer in the Staging Room the drums are transferred to this room. The mixture is poured into the tube-filling machine and is inserted into the consumer tubes. Once filled the technician measures the weight to confirm all tubes are in line with the product specification. The filled tubes are then transferred to the Intermediate Room.
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Tube-Filling Room


After the mixture has cooled down and approval has been granted by the Quality Control Officer in the Staging Room the drums are transferred to this room. The mixture is poured into the tube-filling machine and is inserted into the consumer tubes. Once filled the technician measures the weight to confirm all tubes are in line with the product specification. The filled tubes are then transferred to the Intermediate Room.
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Retained Samples Room


This room is assigned to storing retention samples. A retention sample is a sample taken from each batch of finished products prior to being dispatched to the market. The samples are stored under controlled conditions to replicate market retail storage conditions.


The purpose of retaining samples is to be used as a reference in the case of any customer complaint investigations.


The quality control officer occasionally undertakes relevant tests on the retained samples to ensure the quality remains consistent in line with the products’ shelf-life.
The samples are disposed one year after the product expiry date.



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Retained Samples Room


This room is assigned to storing retention samples. A retention sample is a sample taken from each batch of finished products prior to being dispatched to the market. The samples are stored under controlled conditions to replicate market retail storage conditions.


The purpose of retaining samples is to be used as a reference in the case of any customer complaint investigations.


The quality control officer occasionally undertakes relevant tests on the retained samples to ensure the quality remains consistent in line with the products’ shelf-life.
The samples are disposed one year after the product expiry date.



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Mixer No. PD-26


This machine is used to pilot new formulas after they have been developed in the Research & Development Lab. This process will imitate the production environment of the bigger machines to ensure a lean manufacturing process. The machine has a capacity of producing 100kg of mixture per cycle.
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Mixer No. PD-26


This machine is used to pilot new formulas after they have been developed in the Research & Development Lab. This process will imitate the production environment of the bigger machines to ensure a lean manufacturing process. The machine has a capacity of producing 100kg of mixture per cycle.
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Air Lock (2)


After one batch is released from the Raw Material Warehouse and Packaging Material Warehouse, it enters the Airlock area where the Warehouse Keeper temporarily places the required raw material and packaging material required. The Production Supervisor then confirms the quantities in the presence of the Quality Assurance Officer and transfers the material onto the Intermediate Store.



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Air Lock (2)


After one batch is released from the Raw Material Warehouse and Packaging Material Warehouse, it enters the Airlock area where the Warehouse Keeper temporarily places the required raw material and packaging material required. The Production Supervisor then confirms the quantities in the presence of the Quality Assurance Officer and transfers the material onto the Intermediate Store.



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Intermediate Room


Intermediate Room is where the raw material and packaging material are placed, before commencing onto the full process of the secondary packaging phase. Only one full batch can be placed in the Intermediate store before having it moved incrementally onto the production process. Once this batch is used up completely, the intermediate store is replenished with another full batch.


All materials within this store must be assigned an identification label which encompasses the product name, manufacturing date, expiry date, batch number and Quantity numbers. This includes Quality Control numbers to prove the item has met quality standards.


The Quality Assurance Officer then hands over the batch records to the Production Officer. A batch record is a document which records the entire production process from start to finish to maintain an internal and external audit trail.



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Intermediate Room


Intermediate Room is where the raw material and packaging material are placed, before commencing onto the full process of the secondary packaging phase. Only one full batch can be placed in the Intermediate store before having it moved incrementally onto the production process. Once this batch is used up completely, the intermediate store is replenished with another full batch.


All materials within this store must be assigned an identification label which encompasses the product name, manufacturing date, expiry date, batch number and Quantity numbers. This includes Quality Control numbers to prove the item has met quality standards.


The Quality Assurance Officer then hands over the batch records to the Production Officer. A batch record is a document which records the entire production process from start to finish to maintain an internal and external audit trail.



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Mixer No. PD-27


The largest mixer in the room, this mixing machine has a capacity of 2,000kg per mixture. A 2,000kg mixture takes about four hours to complete.
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Mixer No. PD-27


The largest mixer in the room, this mixing machine has a capacity of 2,000kg per mixture. A 2,000kg mixture takes about four hours to complete.
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Cosmetics Finished Products Warehouse


It is a ventilated, temperature and humidity-controlled area where cosmetics finished products are stored in line with Good Manufacturing Practice standards. The finished products are organized in shipping boxes and are clearly labeled with their specifications. The products are organized according to product line and purchase order in preparation for dispatch to distributors.


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Cosmetics Finished Products Warehouse


It is a ventilated, temperature and humidity-controlled area where cosmetics finished products are stored in line with Good Manufacturing Practice standards. The finished products are organized in shipping boxes and are clearly labeled with their specifications. The products are organized according to product line and purchase order in preparation for dispatch to distributors.


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Discharge Room


An area where the raw material received from the Intermediate Store is organized for the secondary packaging process. Any excess material that is not required for packaging is disregarded and recycled.


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Discharge Room


An area where the raw material received from the Intermediate Store is organized for the secondary packaging process. Any excess material that is not required for packaging is disregarded and recycled.


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Finished Product Area


This is the area where finished products are received after completion of the packaging process.


The Quality Assurance Officer here confirms that the total quantity of received packs are in line with the batch records and crosschecks that the specifications of the finished products match the details of the respective batch record. Once approved, the Quality Assurance Officer add a “Released” label to all finished packs.



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Finished Product Area


This is the area where finished products are received after completion of the packaging process.


The Quality Assurance Officer here confirms that the total quantity of received packs are in line with the batch records and crosschecks that the specifications of the finished products match the details of the respective batch record. Once approved, the Quality Assurance Officer add a “Released” label to all finished packs.



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Mixer No. PD-16


This machine has a capacity of 1,000kg per mixture. One mixture takes about two hours to complete.
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Mixer No. PD-16


This machine has a capacity of 1,000kg per mixture. One mixture takes about two hours to complete.
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Receiving Area


The area where primary and secondary packaging material is first admitted to the factory.


First, the Warehouse Keeper confirms the quantities received.
Second, the Quality Control Officer assigns the quality control receiving numbers per category of material. This is used as an internal tracking system.


Third, the Quality Assurance Officer generates an incoming identification label to place onto the packaging material. This label includes information about the Material Name, Batch Number, Manufacturing date, Expiry Date (if applicable) and Quality Control Receiving Numbers.




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Receiving Area


The area where primary and secondary packaging material is first admitted to the factory.


First, the Warehouse Keeper confirms the quantities received.
Second, the Quality Control Officer assigns the quality control receiving numbers per category of material. This is used as an internal tracking system.


Third, the Quality Assurance Officer generates an incoming identification label to place onto the packaging material. This label includes information about the Material Name, Batch Number, Manufacturing date, Expiry Date (if applicable) and Quality Control Receiving Numbers.




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Tube-Filling Machine No. PD-011


This machine is specific for filling aluminum and laminated tubes with semi-solid mixtures. The machine can fill up to 1,000 tubes per hour.
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Tube-Filling Machine No. PD-011


This machine is specific for filling aluminum and laminated tubes with semi-solid mixtures. The machine can fill up to 1,000 tubes per hour.
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Airlock (7)



The purpose of an airlock is to allow for a shift between cleanliness levels and avoid cross contamination.
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Airlock (7)



The purpose of an airlock is to allow for a shift between cleanliness levels and avoid cross contamination.
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Airlock (1)



Once the products are fully packaged in their respective shipping boxes, the production staff temporarily places the cartons in the Airlock. Next, the Warehouse Keeper transfers the items from the Airlock to the Finished Products Warehouse.
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Airlock (1)



Once the products are fully packaged in their respective shipping boxes, the production staff temporarily places the cartons in the Airlock. Next, the Warehouse Keeper transfers the items from the Airlock to the Finished Products Warehouse.
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3R Pharmaceutical Industries is a manufacturing facility that introduces the innovative idea of licensed manufacturing and secondary packaging in order to support principals in facilitating the registration of pharmaceuticals, medical devices, and cosmetic products to the Jordanian and MENA market using alternative business models.


To explore our facilities please use the animated arrows and circles to move around, you can also use the interactive floorplan to go to the designated areas.
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3R Pharmaceutical Industries is a manufacturing facility that introduces the innovative idea of licensed manufacturing and secondary packaging in order to support principals in facilitating the registration of pharmaceuticals, medical devices, and cosmetic products to the Jordanian and MENA market using alternative business models.


To explore our facilities please use the animated arrows and circles to move around, you can also use the interactive floorplan to go to the designated areas.
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Antiseptic & Disinfectants Production Area


This room is specific for the filling of antiseptic & disinfectant products, including printing of batch details on the packaging. The released mixtures such as Rubbing Alcohol, Alcohol gels and Liquid Disinfectant Soaps are first filled into their designated packaging and are then labelled using the same machine with the batch number, production date and expiry date.



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Antiseptic & Disinfectants Production Area


This room is specific for the filling of antiseptic & disinfectant products, including printing of batch details on the packaging. The released mixtures such as Rubbing Alcohol, Alcohol gels and Liquid Disinfectant Soaps are first filled into their designated packaging and are then labelled using the same machine with the batch number, production date and expiry date.



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Chemical lab


The Quality Control Officer uses this lab to analyse and test the physical and chemical qualities of raw materials, work-in-progress goods, and finished products. This ensures all materials meet the required specifications.
Analyzing the chemical components includes PH and conductibility tests, moisture analysis, and titration.
The physical assessment includes examining the texture of the primary product and the outer packaging for any defects in appearance.


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Chemical lab


The Quality Control Officer uses this lab to analyse and test the physical and chemical qualities of raw materials, work-in-progress goods, and finished products. This ensures all materials meet the required specifications.
Analyzing the chemical components includes PH and conductibility tests, moisture analysis, and titration.
The physical assessment includes examining the texture of the primary product and the outer packaging for any defects in appearance.


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Mixer 1000 Kg for Iodine


This is a mixer for liquids and has a capacity to fill 1,000kg of liquid per cycle which takes about 3 hours to complete



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Mixer 1000 Kg for Iodine


This is a mixer for liquids and has a capacity to fill 1,000kg of liquid per cycle which takes about 3 hours to complete



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Aerofill Machine PD-024


This machine is for filling gas in spray cans. It can fill up to 1,200 70ml bottles per hour.



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Aerofill Machine PD-024


This machine is for filling gas in spray cans. It can fill up to 1,200 70ml bottles per hour.



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Packaging Room (1)


The area where the raw material is packed in specific boxes with their respective leaflets and organized in their identified outer cartons for shipping.
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Packaging Room (1)


The area where the raw material is packed in specific boxes with their respective leaflets and organized in their identified outer cartons for shipping.
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Quarantine Area


This is the second step after the receiving area. Here, the raw material and packaging material are entered after being labelled in the Receiving Area.


The Quality Assurance Officer here includes a “HOLD” label onto all material for further inspection.


As for the Quality Control Officer, they conduct sampling and testing procedures to check the physical quality and precision of the received goods before moving them onto the Released stores. This inspection includes: packaging and content defects, measurements of pack dimensions, and identification labels.


Once the material is approved for transfer, the Quality Control officer adds a “RELEASED” label onto all Received Goods.





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Quarantine Area


This is the second step after the receiving area. Here, the raw material and packaging material are entered after being labelled in the Receiving Area.


The Quality Assurance Officer here includes a “HOLD” label onto all material for further inspection.


As for the Quality Control Officer, they conduct sampling and testing procedures to check the physical quality and precision of the received goods before moving them onto the Released stores. This inspection includes: packaging and content defects, measurements of pack dimensions, and identification labels.


Once the material is approved for transfer, the Quality Control officer adds a “RELEASED” label onto all Received Goods.





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Raw Material Warehouse


It is a temperature and humidity controlled area where raw material approved by the Quality Control officer is stored in line with best practices. From here, the raw material is then incrementally delivered onto the Intermediate Store within the production area based on the production batch in demand.


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Raw Material Warehouse


It is a temperature and humidity controlled area where raw material approved by the Quality Control officer is stored in line with best practices. From here, the raw material is then incrementally delivered onto the Intermediate Store within the production area based on the production batch in demand.


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Receiving Area


This is a temperature-controlled area where raw material as well as packaging materials are first admitted as a primary point of entry. Here, the quantities are checked by the warehouse keeper and the Quality Control officer who initiates Quality Control Receiving Numbers to the packaging material only.


Additionally, the Quality Assurance officer here adds an incoming identification label onto the packaging material (Such as the Product Name, Batch Number, Manufacturing date, Expiry Date and Quality Control Receiving Numbers).


As for the raw material, they already have identification labels from the manufacturing company, however if the specifications are unclear, the Quality Assurance officer adds an identification label onto all the raw material.


Once cleared, the material is then transferred to the Quarantine Area.



HTMLText_B06E34F7_916A_3783_41DF_7DF3EF06EFD1_mobile.html =
Receiving Area


This is a temperature-controlled area where raw material as well as packaging materials are first admitted as a primary point of entry. Here, the quantities are checked by the warehouse keeper and the Quality Control officer who initiates Quality Control Receiving Numbers to the packaging material only.


Additionally, the Quality Assurance officer here adds an incoming identification label onto the packaging material (Such as the Product Name, Batch Number, Manufacturing date, Expiry Date and Quality Control Receiving Numbers).


As for the raw material, they already have identification labels from the manufacturing company, however if the specifications are unclear, the Quality Assurance officer adds an identification label onto all the raw material.


Once cleared, the material is then transferred to the Quarantine Area.



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Labeling Machine No. PD-40


This machine is specific for labelling bottles with rounded dimensions.
The machine has the capacity to label up to 900 bottles per hour.


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Labeling Machine No. PD-40


This machine is specific for labelling bottles with rounded dimensions.
The machine has the capacity to label up to 900 bottles per hour.


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Packaging Material Warehouse


It is a temperature and humidity controlled area where packaging material approved by the Quality Control officer is stored in line with best practices. From here, packaging material are then incrementally delivered onto the Intermediate Store within the production area.



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Packaging Material Warehouse


It is a temperature and humidity controlled area where packaging material approved by the Quality Control officer is stored in line with best practices. From here, packaging material are then incrementally delivered onto the Intermediate Store within the production area.



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Printing Area


The area where batch numbers, manufacturing and expiry dates are printed onto each product box using our dedicated printing machine.


Before printing commences, the Quality Assurance Officer confirms that the printing machine has been properly calibrated by inspecting a few samples.



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Printing Area


The area where batch numbers, manufacturing and expiry dates are printed onto each product box using our dedicated printing machine.


Before printing commences, the Quality Assurance Officer confirms that the printing machine has been properly calibrated by inspecting a few samples.



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labeling Room


The room where labels are stickered on bottles with the help of a designated labeling machine.
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labeling Room


The room where labels are stickered on bottles with the help of a designated labeling machine.
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Packaging Room (2)


The area where the raw material is packed in specific boxes with their respective leaflets and organized in their identified outer cartons for shipping.
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Packaging Room (2)


The area where the raw material is packed in specific boxes with their respective leaflets and organized in their identified outer cartons for shipping.
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Air Lock 1


Once the products are fully packaged and organized in their respective shipping boxes, the production staff temporarily places the cartons in the Airlock. Next, the Warehouse Keeper transfers the items from the Airlock to the Finished Products Warehouse.



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Air Lock 1


Once the products are fully packaged and organized in their respective shipping boxes, the production staff temporarily places the cartons in the Airlock. Next, the Warehouse Keeper transfers the items from the Airlock to the Finished Products Warehouse.



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G 230i Thermal Ink Jet


The ink used in this process has been approved by the Jordanian FDA. The machine can print up to 1,500 units per hour.
HTMLText_B78D3DA2_9176_31BD_41CA_3E3C83C1B5D2_mobile.html =
G 230i Thermal Ink Jet


The ink used in this process has been approved by the Jordanian FDA. The machine can print up to 1,500 units per hour.
HTMLText_B78DCDA0_9176_31BD_41B9_C29E203BB35A.html =
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