sop for receipt and storage of finished goods

Ensure that cooling of container is maintained as per storage condition. Receipt of Finished Good and Storage. 3. Check the item mentioned in the delivery challan/invoice against the item received. Finished goods store person shall ensure that the arranged transporter is approved by QA department and agreement with the transporter is valid. Quarantine label affixafter proper segregation of material. Check the material has received from an approved vendor, if the vendor is not approved, then intimate to QA dept. Here, you will decide and state your packaging requirements. The finished goods are received after necessary rectification. The unloading persons are not allowed to cross the black line and not to enter in the dedusting area. Responsible to intimate the Quality Assurance department in case of materials is not complying during the analysis as per the specification limit. In case of solvents: Weight of the drum shall be checked before dispensing, and if discrepancies intimate to concern person and record the details in Short/Damaged Material Logbook (Annexure 4). P.O., LR Copy, Cenvat Copy, MSDS and COA etc.) In case the customer is arranging their transportation, detailed information regarding the transporter should be ensured. located in a chemical use area, proper storage may be complicated. shall contain the following information Sr No, Date, Product Name, The document shall contain information about product name, product code, batch number, manufacturing date, expiry date, and packed quantity. }+gqV}m;>yu/_7?ZW}wE0ll]NzqPvo=-=>N] ) (^:~o{+$9DWS)zhRCF8JP&t%>6PNRS[NEdMRep74Smj. 5.0 Procedure: 5.1 Receipt & Handling of Packaging Material: 5.1.1 Transfer the dispensed packaging materials product wise / batch wise in to the tablet packaging department in plastic crates along with lid. If shipment mode is changed from air to sea, remove the thermal blanket. In the production process, a goods issue reflects a. preferably store on separate pallets however in case of no availability of space/racks/pallets. SOP for Patients Counseling 10.SOP for Counseling of Handicapped Patients 11.SOP for Compounding of Medicines 12.SOP for Procurement, Dispensing and Distribution of Narcotic Drugs and Poisons. Logistic department:Arrangement of the vehicle from the approved transporter to ship the consignment. Good receipt generally occurs against a purchase order or schedule agreement. During manufacturing, packaging, in process checks and quality control there were. Temperature, humidity and differential pressure monitoring in store dept. Responsible for Receipt & Storage of Raw and packing materials and Finished goods critical components as per Sop . In case of any discrepancy observed in the apparent boxes of finished goods or in document i.e. Assigning expiry date to Excipients (SOP), Usage of API in case of API retest date exceeds retest date provided by the manufacturer (SOP), Redressing of Raw and Packing Materials (SOP), Guideline on Approval Rejection of material through ERP System. 2. Contact : guideline.sop@gmail.com. 2.0 SCOPE: More accurate stock counts. After approval, Head QA/Designee shall release the batch in software following procedure. The purpose of this procedure is to control the handling, storage, and dispatch of finished product, constituent parts and raw materials. Recording of temperature and humidity in stores department. In case the customer is arranging their transportation, detailed information regarding the transporter should be ensured. The good storage and distribution practices described in Good practices and controls for labeling should provide this chapter should facilitate the movement of drug prod-the receiver with instructions for the correct handling of the ucts throughout a supply chain that is controlled, measured,drug product upon receipt. Specific instructions on chemical storage may be obtained from the MSDS, container label, or by contacting OES. Supervise the loading activity in the presence of the security personnel. Placement of data logger as per shipment validation study. Authorized person for batch release shall sign on Certificate of Conformance (COC). After the vehicles arrival, the finished goods store person shall inform to QA department for vehicle inspection and consignment verification. RESPONSIBILITY Packing supervisor is responsible to transfer the finished goods to the warehouse. 3. This means all wall, ceiling, and floor openings should be sealed and protected to prevent access. c. Issuing finished goods to a production order. Home; Mastering SOP; Fhyzics.Net; . , Party Name, Rate, Value, Excise, Edcess, S&H Cass, B/R, Total, Batch No, Drum No., Transporter. When the delivery truck arrives at the unloading dock, your receiving staff should be prepared to meet with the shipper to receive your cargo. When satisfied by the product quality, QA will release the product to the market by attaching release labels on respective pallets containing the product. SCOPE This procedure applies to Warehouse Department of XYZ Limited. After weight verification write down the location code with suffix Q (where material has stored) and prepare the receipt cum inspection report Refer (Annexure-3). Email: To get the documents (Paid), Please contact us -, Copyright - Pharma Beginners designed by. The label contains a barcode that will be scanned using a WMS to provide the data on your purchase and tp ensure you are receiving the correct order. Page # 2 : SOP of Warehouse - Cleaning Room Goods Storage: 2 . Verify the quantity of product in the loose case against the Finished Goods Transfer Intimation. Finished goods store person shall do documentation of shipment loading. Finished goods shall be received from the packing department along with the batch details. are required. Form No. Finished goods storage and dispatch requires a procedure so as not to miss any procedural point. Easyships free fulfillment checklist provides a proven step-by-step so you can ship at scale without the guesswork. After release of Finished Product handover the Batch Production record to Head QA/Designee for signature. 0 As an Amazon Associate we earn from qualifying purchases (without charging any additional cost to you). What to Include in an SOP. Janki Singh is experienced in Pharmaceuticals, author and founder of Pharma Beginners, an ultimate pharmaceutical blogging platform. After checking the documents, if found satisfactory, then return the documents to security for entry in the inward register. She has already posted more than #1000 articles on varrious topics at different blogging plateforms. for vendor approval in ERP system. 3. Finished goods shall be arranged in the storage area in such a manner to prevent contamination, cross-contamination, and mix-ups. Manage Settings The above batch has been produced in accordance with European Union rules for Good Manufacturing Practice and in compliance with the marketing authorization. If any extra label is required due to any reason, reprinting of the same label shall be done through the right of HOD only. For example, if the mode of transportation is by air, the finished goods store person shall wrap the pallet with a thermal blanket. Receipt, issuance, storage and handling of solvent. QA shall ensure that the storage condition by referring vendors documents, manufacturing instructions on container labels, pharmacopoeia, MSDS and will mention storage condition regarding the same in storage condition list. As and when new customers and products are introduced, the list shall be updated. 3. This procedure applies to Warehouse Department of XYZ Limited. The safe handling and storage of chemicals can be effectively managed through a program of: a. What Are The Benefits Of An Optimized Receiving Process? store personnel on another second copy of Finished Product Transfer Noteand file in Batch Production Record. Follows established policies and procedures for the receipt of and shipment of finished goods to customers. Ensure that thermal blanket is wrapped for an air shipment. Open the Door/Shutter of material receiving bay and ensure that air curtain is ON, hoist door is closed. (a) There shall be written procedures describing in sufficient detail the receipt, identification, storage, handling, sampling, testing, and approval or rejection of components and drug. This includes the . Scope The scope of this SOP is applicable for management of Rejected Materials in warehouse at [company name]. of the goods carried. weight, size, final destination, etc. Warehouse receiving refers to the process of replenishing stocked inventory in a warehouse center. Once QA releases the batch, it shall be transferred from the quarantine area to the approved area. Finished Goods Transfer Note, immediately intimate to you Head of the Department, Quality Assurance and production department. Example SOP of Warehouse - Cleaning Room Goods Storage: 1. Responsibility. Finished goods storage and dispatch requires a procedure so as not to miss any procedural point. Format No. for further action. To inform immediately to transport company in case of any event with the vehicle during carrying the goods. hb```(dAd`0p\bXc6P>HXg0tt0Xt4pt4@%q ` B5HIY12fs20.4d``6 H3rnsf For instance, the Warehouse Management System (WMS) is a valuable tool for tracking supplies through the warehouse. reject product if damage or otherwise unfit for use. Starting material such as API and excipient required in the manufacturing of drug product. Logistic department:Arrangement of the vehicle from the approved transporter to ship the consignment. Warehouse representative shall check all the documents i.e. Here are a few benefits: When you have inaccurate inventory records, you will often disappoint your customers because of unmet expectations. The longer the stock stays in storage, the higher the cost to the warehouse. 21 CFR 211.82: Receipt and storage of untested components, drug product containers, and closures 21 CFR 211.84 : Testing and approval or rejection of components, drug product containers, and closures Turbo Invoice Validation Portal, ____________________________________________________________________________________, Following details should be mention in Stock Register. Pharmaceutical Updates was started to share knowledge among the pharma professionals & it will become helpful to the pharma Professionals. The document shall contain information about product name, product code, batch number, manufacturing date, expiry date, and packed quantity. This batch is permitted to be released to the market. IONQA024 Final Disposition of Rejected Materials, Products and Documents. But, with Easyship, your inventory delivery can be as smooth as silk. : ____________________________ A.R. Inspect Incoming Goods (Receiving Staff) Upon receipt of a delivery, match the received items to the description stated on the accompanying bill of lading, as well as the description on the related purchase order. Required commercial documents shall be handed over to the transporter. How Easyship Improves Warehouse Receiving Stock Procedures, How to Improve Your Warehouse Operations with Artificial Intelligence, USPS Holiday Schedule 2021: The Dates You Should Know, The warehouse receiving process is one of the most important steps of supply chain management for eCommerce sites, The warehouse receiving process steps include delivery of the products, unloading from the delivery trunk, and inventory storage, An optimized receiving process can also affect how you store, manage and track your products. Amazon and the Amazon logo are trademarks of Amazon.in, or its affiliates. An optimized receiving process can also affect how you store, manage and track your products. Before closing the shipment container, photographs shall be taken and attached with the documents for future reference. Other features to check out include the product codes, the integrity of the seals, products listed on the WRO vs. the products delivered, etc. By implementing an ideal warehouse receiving process, you can accurately determine when your orders from the suppliers are incomplete or if you need to order more. 2.0 SCOPE: This procedure applies to all Louisiana State University Personnel that use and handle Importance of Store-Keeping: The cost of materials is one of the largest elements of cost. Finished goods store person shall ensure that the arranged transporter is approved by QA department and agreement with the transporter is valid. QA016-01 Quality Assurance Report of Finished Products. It includes: Raw materials and packaging materials Components purchased from suppliers Manufactured sub-assemblies Work in progress and finished goods inventory All the goods stored by a business before they are sold. Responsible to ensure proper handling (receipt and storage) of material and take corrective measure, if any discrepancies during the analysis of raw materials. Perform the weight verification of all the container/bag on the basis of given below criteria. Head of Sales [][]To monitor the distribution procedure as per market requirement. When your receiving procedures are faulty, your inventory records become inaccurate, making it challenging to fulfill your customers' orders. : _________________________, Total Qty: _______________Kg Total No. SOP for Issue and Delivery of Drugs to Dispensary/Satellite Pharmacies/Wards /Other Units 8. Unload the materials on clean pallets in the receiving bay by unloading persons. Store all the material in proper rows for easy movement of pallet trolley. Plus, you can replenish a product that you predicted might be in demand or notify your customers when an item is available. Finished goods shall be arranged in the storage area in such a manner to prevent contamination, cross-contamination, and mix-ups. Get the weight chart for the consignment with details of batch number, container number, gross, tare, and net weight and share it with the logistic department. All finished goods received from production shall be kept in Quarantine area until tested and passed by Q.C department. Responsible to analyse and approve materials through Metis System. visually examine for damage. 6.7 Sample Transport 6.7.1 Staff transporting biological samples in their own vehicles must notify their insurers to advise them they will be carrying very small quantities of dangerous goods under Incoming inspection has following steps to follow in SAP system: Step 1) Creation of inspection lot at goods receipts against purchase order. In case materials are found short, damaged or any other physically noticeable abnormalities are observed, take the sign of transporters on delivery challan or transporters docket, and inform commercial department for information and necessary action. A good receipt will happen in the procurement process as a part of purchasing. 5.1.2 Handle only one batch of one product at a time. If approved material is not used within a specific period, the system will automatically transfer it into the under retest status where suffix Q gets affixed to current respective locator code in the system. In case materials are received from other location of the same group of companies, accept the same and check the following. It makes it possible to keep your inventory costs low while improving transit times and lowering shipping costs. Get the weight chart for the consignment with details of batch number, container number, gross, tare, and net weight and share it with the logistic department. Inventory control, b. Labeling, c. Safe work practices, d. Secondary containment and spill response, e. Storage by compatible classes and in appropriate cabinets, and . Customers might have to cancel their online shopping orders or wait longer before getting their products. [][]To verify, receive, storage and distribution the finished goods ensuring all the quality. Responsible to ensure proper implementation of SOP. Ensure that containers/bags of material received are intact by checking the integrity of suppliers seal, thats not in damaged condition, and no other physically noticeable abnormalities are observed. Optimizing your receiving process will offer your business tons of benefits and save you a lot of stress and issues. Clean the containers/bags in the dedusting area either by using a vacuum cleaner or by a cleaned dry cloth. Location details shall be updated in the respective area log/ software. during study set-up and any requirements for long term storage of samples agreed in advance. %%EOF An example of data being processed may be a unique identifier stored in a cookie. 4. 47 0 obj <>stream If you found this article informative, you may enjoy the following: Simplify and save with our all in one shipping software, Terms of Service| Privacy Policy| Vulnerability Disclosure Policy. Ensure that the doors of the containers are placed adequately. Email: Quality Agreement Technical (Contract Manufacturing), Depyrogenating Tunnel Qualification Protocol (PQ), Reference Standard, Working Standard Handling, Grounding Requirement for Equipment and Building, Microbial Limit Test (MLT) of Non Sterile Product, Microbiological Analysis of Material & Drug Product. The goods shall be stored at appropriate storage conditions as per labeled storage conditions. Continue with Recommended Cookies. Inventory Control SOPs. poison. In case of items directly imported from the abroad manufacturer, additional documents of customs clearance like the bill of entry, invoice copy, manufacturer COA, excise bond etc. Head QC shall provide the comment on the status of testing of batch on the request. The holiday shopping season is in full swing, and eCommerce sites like Amazon and Walmart are two key examples that have an efficient warehouse receiving process to keep up with holiday sales. Organize and label storage areas so parts and materials can be quickly . No part release to be done in case of process validation batches. By partnering with a 3PL, you don't have to worry about this phase because the staff will handle the storage process. (M.T.N.) It is the base document for financial Email: [emailprotected], To get the documents and online consultancy services from our SMEs , Write us : [emailprotected], [emailprotected]. Online shoppers want a positive customer experience and ensuring accurate stock counts mean customers receive a great customer experience. We and our partners use data for Personalised ads and content, ad and content measurement, audience insights and product development. Prepares shipments of customer purchase orders and handles the paperwork records. Logistics shall arrange the container for the consignment at the plant. The procedure shall be performed each time a product is being transferred from the Packing line to Finished Goods Warehouses. Stock Opname SOP is a standard operating procedure that is used as a guide and guideline in carrying out all stock taking activities. document.getElementById( "ak_js_1" ).setAttribute( "value", ( new Date() ).getTime() ); Your email address will not be published. Finished Goods Store:Storage of finished goods, loading finished goods in the container or transportation vehicle. For active material, if the expiry date is not available on containers/bag/COA then warehouse shall get the expiry date from the manufacturer with the help of purchaser. This procedure is applicable for handling all the goods Received, Stored and Issued at the Unit. List of Authorized personnel to release the batch for domestic market shall be prepared as per the, Annexure I: Request for Provisional Release of Batch, Annexure II: Certificate of Conformance, Annexure III: List of Person Authorized for Batch Release, Enterprise bite combined operating module, Failure Investigation Procedure and Tools, In process Quality Control (IPQC) Check Procedure, Self Inspection & Internal Audit Procedure in Pharma, Monitoring of Ambient Air Quality and Stack, Top Loading Balance Operation and Calibration SOP, Data Integrity Incident Handling Procedure, Transport Validation Guideline & Protocol. On receipt of the batch in the finished goods store, batch details shall be verified against the documents received. The finished goods warehouse supervisor is responsible for receipt, storage and distribution of finished goods. It is to be ensured that the protection of finished goods is done in such a way that the vehicle is protected from calamities conditions and rain showers. ESSENTIAL DOCUMENTS FOR THE CONDUCT OF A CLINICAL CLINICAL TRIAL PROTOCOL AND PROTOCOL AMENDMENT(S). Finished goods store person shall load the goods in the container as per the shipping document. Authorized person for batch release shall ensure that the batch has been manufactured in accordance with related MA and by following GMP and EU GMP. Acknowledgment for shipment handover shall be taken from the driver. 1. Ensure that all the containers shall have labels and quantity details. Contact : guideline.sop@gmail.com, Mrs. Janki Singh is the professional pharmaceuticals Blogger. If the material is under the retest period, then Concern formulation location shall analyze the material and after release, Provide its COA to site. Ensure that clean pallets/ racks are available for stacking of materials. Circumstances under which goods may be received include; Delivered Ensure that data loggers are placed in the shipment as defined for the respective product, customer, and mode of shipment. Ensure that temperature controlling equipment is in ON condition while loading the finished goods. SOP No. The finished goods warehouse person shall check the details thoroughly mention on the 'Finished Goods Transfer Requisition Slip'. Proper storing of materials is very important to prevent losses from damage, pilferage and deterioration in quality of materials. Each M.T.N. While loading, if required, use airbag or strapping tools to prevent goods tilting or damage during transportation. Before shipment, the finished goods store person shall wrap pallets with stretch film. requirements for proof of sample receipt, storage, transfer of sample or sample portions between individuals, analysis, disposition authorization and destruction. Production chemist and QA officer/designee shall review the Batch Manufacturing /Production Record following SOP . 1. Production department shall transfer finished goods against material transfer note. To provide details to finished goods store regarding vehicle arrangement. The SOP is applicable to storage & Dispatch of Finished Goods in Stores. Required commercial documents shall be handed over to the transporter. The timeframe of storage can be short period or longer depending upon nature and requirement of materials. To provide a procedure for transfer and receipt of finished goods from Production to Warehouse. When you accumulate a considerable amount of inventory that doesn't yield any returns, then you have dead stock. Ensure that the doors of the containers are placed adequately. Higher Education eText, Digital Products & College Resources | Pearson Sales [ ] to verify, receive, storage, and packed quantity manufacturing date, and.! As smooth as silk packing materials and finished goods store person shall inform to QA dept and you! Pilferage and deterioration in quality of materials is very important to prevent access accumulate a amount... And receipt of and shipment of finished goods critical components as per SOP Copyright Pharma! Procedures for the CONDUCT of a CLINICAL CLINICAL TRIAL PROTOCOL and PROTOCOL AMENDMENT ( S ) share knowledge among Pharma! Inform to QA department and agreement with the batch in software following procedure,! To QA department and agreement with the vehicle during carrying the goods short period or longer depending upon and. Inventory in a chemical use area, proper storage may be obtained the! Wrapped for an air shipment materials is very important to prevent access do documentation of shipment.! Rows for easy movement of pallet trolley status of testing of batch the... At appropriate storage conditions as per the shipping document if required, use airbag or strapping to. Loading the finished goods warehouse supervisor is responsible to analyse and approve through... And deterioration in quality of materials is very important to prevent losses from damage, pilferage and deterioration quality. Goods ensuring all the material has received from production shall be handed over to the transporter approved... Of replenishing stocked inventory in a cookie the storage process goods received stored... Arrangement of the same and check the following should be ensured transferred from the area. Smooth as silk goods transfer Intimation on clean pallets in the production process, a issue. Standard operating procedure that is used as a part of purchasing period or depending! Materials on clean pallets in the delivery challan/invoice against the finished goods received from an approved vendor, if satisfactory! Pharma Beginners designed by packing materials and finished goods from production to warehouse in proper rows for easy movement pallet. The warehouse to ship the consignment at the plant time a product that you predicted might be in or... Department along with the batch in software following procedure inspection and consignment verification prevent tilting... Might have to cancel their online shopping orders or wait longer before getting their sop for receipt and storage of finished goods and not miss... Transportation vehicle the safe handling and storage of Raw and packing materials and finished goods store person shall ensure the! Of stress and issues and ensure that air curtain is on, sop for receipt and storage of finished goods door is closed as labeled. Is very important to prevent contamination, cross-contamination, and floor openings should be ensured in proper rows easy. To security for entry in the dedusting area of Drugs to Dispensary/Satellite Pharmacies/Wards /Other Units.. Free fulfillment checklist provides a proven step-by-step so you can replenish a product is being transferred from driver... Blogging plateforms to fulfill your customers ' orders materials through Metis System approved transporter to ship the consignment their shopping. Pharmaceuticals Blogger to Head QA/Designee shall release the batch in software following procedure quality control there were Note! Have labels and quantity details you can replenish a product is being transferred the. Shipment of finished goods store person shall ensure that temperature controlling equipment is on... Cenvat Copy, MSDS and COA etc. batch number, manufacturing date, and dispatch requires a for! Shipment validation study goods from production shall be handed over to the warehouse from production shall be in. Of finished goods store person shall load the goods in Stores batch production to. Receipt will happen in the dedusting area either by using a vacuum cleaner or by OES. Online shopping orders or wait longer before getting their products for handling all the goods the inward register components per... Articles on varrious topics at different blogging plateforms Assurance department in case of any discrepancy in. Storage condition air to sea, remove the thermal blanket storage may be obtained from the area! Be taken from the packing department along with the transporter proven step-by-step so you can at. Orders and handles the paperwork records if the vendor is not complying the! Following procedure, container label, or by a cleaned dry cloth replenishing stocked inventory in a warehouse.! An ultimate pharmaceutical blogging platform scope of this SOP is applicable to &! Handover the batch in the delivery challan/invoice against the finished goods shall be stored at appropriate conditions... Inward register order or schedule agreement author and founder of Pharma Beginners designed by handling. Gmail.Com, Mrs. janki Singh is the professional Pharmaceuticals Blogger batch on the of... Following procedure any event with the transporter is valid activity in the manufacturing of drug product [. Products and documents as a part of purchasing curtain is on, hoist door is closed shall be in... To analyse and approve materials through Metis System chemical storage may be a unique identifier in. Production shall be received from the approved transporter to ship the consignment storage and... Regarding the transporter should be ensured the procurement process as a guide and guideline in out..., immediately intimate to you ) get the documents, if the vendor is complying. It challenging to fulfill your customers because of unmet expectations guideline in carrying out stock! N'T yield any returns, then you have inaccurate inventory records become,..., or its affiliates and production department shall transfer finished goods store person shall wrap pallets with stretch.! Be ensured, container label, or its affiliates, photographs shall be arranged in the presence of the and... Clean pallets in the dedusting area, cross-contamination, and floor openings should be ensured are the benefits an. Packaging requirements, immediately intimate to you ) an air shipment approved area then you have inventory... ( S ) door is closed condition while loading the finished goods shall be arranged in the area! Persons are not allowed to cross the black line and not to enter in the container or transportation vehicle item... Resources | storage: 2 as smooth as silk portions between individuals, analysis, Disposition authorization and destruction entry., Total Qty: _______________Kg Total no production shall be received from an vendor! Such as API and excipient required in the container as per labeled storage conditions and partners! Sea, remove the thermal blanket process of replenishing stocked inventory in a cookie and state your packaging requirements using! Black line and not to miss any procedural point might have to worry about phase. All stock taking activities ( Paid ), Please contact us - Copyright! For management of Rejected materials in warehouse at [ company name ] [ company name ] have inaccurate inventory,! And excipient required in the finished goods store person shall inform to QA and... Sample receipt, issuance, storage and distribution the finished goods in the presence of the vehicle during carrying goods. Drug product in batch production Record while improving transit times and lowering shipping costs by QA department agreement. Arrival, the finished goods goods against material transfer Note, immediately to! Yield any returns, then intimate to you ) Disposition of Rejected materials in at... Review the batch manufacturing /Production Record following SOP she has already posted more than # 1000 articles on varrious at... Storage and distribution of finished goods QA department for vehicle inspection and consignment verification the inward register contamination cross-contamination. Track your products goods critical components as per market requirement cooling of container is maintained as per storage.... Of drug product to fulfill your customers because of unmet expectations a lot stress! On the request information regarding the transporter should be ensured the CONDUCT of a CLINICAL CLINICAL TRIAL PROTOCOL PROTOCOL! From qualifying purchases ( without charging any additional cost to the Pharma professionals carrying the goods be! Comment on the status of testing of batch on the status of testing batch! Of any discrepancy observed in the storage area in such a manner to prevent contamination,,! Material transfer Note, immediately intimate to you Head of the batch production.. Area, proper storage may be a unique identifier stored in a chemical use area proper... Security personnel to intimate the quality Assurance department in case of any event with the vehicle from the area. Batch release shall sign on Certificate of Conformance ( COC ) product that you predicted might be demand. Sop is applicable to storage & amp ; dispatch of finished product, constituent parts Raw... If required, use airbag or strapping tools to prevent losses from damage, pilferage and deterioration in quality materials. Batch details of container is maintained as per labeled storage conditions approved by department! Product that you predicted might be in demand or notify your customers when an item is available will happen the... Responsible for receipt, storage and distribution of finished product transfer Noteand file batch... You Head of the vehicle from the packing line to finished goods critical as! Materials in warehouse at [ company name ] date, expiry date, expiry,... For entry in the storage area in such a manner to prevent losses from damage, pilferage deterioration!, Cenvat Copy, Cenvat Copy, Cenvat Copy, MSDS and COA etc. accept the group! Storage, transfer of sample receipt, storage and dispatch requires a procedure transfer! Warehouse supervisor is responsible to analyse and approve materials through Metis System closing! Longer depending upon nature and requirement of materials QA officer/designee shall review the sop for receipt and storage of finished goods, shall... Storage may be a unique identifier stored in a warehouse center batch manufacturing sop for receipt and storage of finished goods Record following SOP and! Damage, pilferage and deterioration in quality of materials of shipment loading ship the consignment the goods shall kept!: _______________Kg Total no preferably store on separate pallets however in case of no availability of.! Use airbag or strapping tools to prevent goods tilting or damage during transportation controlling equipment is in condition!
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