My Pet FloraUP is an independently developed project by AllBio and is the only gut microbiota testing service in Taiwan specifically designed for pets. Using next-generation sequencing (NGS) technology, this test deciphers the microbial communities hidden in pets’ intestines. My Pet FloraUP utilizes sequencing instruments produced by Illumina, a market leader with a 90% market share. These advanced sequencing systems enable rapid data acquisition, significantly reducing the time required for sequencing.
Once sequencing is completed, the data is analyzed using AllBio's proprietary pet gut microbiota database and the self-developed iFlora algorithm. The test report includes probiotic and pathogenic bacteria analysis, health risk assessments, dietary type analysis, probiotic supplementation recommendations, and antibiotic usage suggestions. With this comprehensive report, professional veterinarians can provide personalized dietary recommendations, probiotic supplementation guidance, and dietary adjustment plans tailored to the individual pet’s needs.
Components of the My Pet FloraUP Sampling Kit:
My Pet FloraUP Sampling Kit Box: Outer packaging for the kit.
Testing Application Form (in triplicate): Used for submitting test requests.
Sampling Tube (with preservation solution): A tube containing a liquid preservative for the sample.
Label Stickers: For labeling the sample tube and form.
Biohazard-Protective Zipper Bag: For safely storing and transporting the sample.
Prepaid Courier Slip and Convenient Delivery Bag: For sample return shipping.
Material Information:
Paper Materials: Sampling kit box, testing application form (in triplicate), label stickers, and prepaid courier slip.
Plastic Materials: Sampling tube (with preservation solution), biohazard-protective zipper bag, and delivery bag.
製造廠名稱: AllBio Life, Inc, 製造廠登記: TAF ISO17025 4186, 製造廠品管: Other(ISO17025)
Establish a method for managing record forms and responsibilities to facilitate the effective operation and verification of the quality system. Ensure that laboratory quality system records are easy to read, identify, and retrieve, serving as a basis for future quality improvements and traceability.
Focus on quality control of raw materials, semi-finished products, and finished products, as well as process management, to comply with ISO laboratory standards.
To ensure proper quality control of finished products, establish procurement and inventory management procedures to ensure that the required supplies or services are supplied and accepted in a timely, appropriate, and adequate manner. Regular inventory checks should also be carried out.
Receiving, Acceptance, and Review of Goods
Once the supplier delivers the goods, relevant personnel must confirm the following: item type, model, specifications, quantity, expiration date, shelf life, and whether they match the procurement requirements. Additionally, they should ensure the appearance, packaging, and transportation temperature are correct before signing the delivery receipt. The administrative assistant will retain a copy of the delivery receipt, and the goods will be placed in a designated inspection area under proper storage conditions pending acceptance. Any non-compliant goods can be immediately rejected and returned. Complete the "Supply Inspection Checklist" to verify that all acceptance criteria are met, including:
Whether the receiving process is fully completed.
Whether storage temperatures meet requirements.
Whether the product can be used within the validity period.
Whether the COA (Certificate of Analysis) and MSDS (Material Safety Data Sheet) documents are accurate.
Whether the product insert (Packing Insert) is provided or updated.
Whether testing is required, and if tested, whether the goods meet standards.
Once goods pass inspection, relevant personnel should mark the goods with an acceptance label and the acceptance date, after which the goods can be stored in the inventory. If the goods fail the receiving or acceptance process, they must not be accepted. Non-compliant goods should be placed in the return zone, clearly labeled as prohibited for use, and the supplier should be immediately notified to arrange for a return or replacement.
Inventory and Stock Control
Establish safety stock controls for raw materials, reagents, and consumables, and conduct inventory checks every six months. Record inventory movements in the "Reagent and Consumable Inventory Management Form" and submit them for supervisor review. The administrative assistant should evaluate goods nearing safety stock levels to determine whether procurement is necessary to avoid stock shortages.
