propofol
I have found results from20+products and8suppliers aboutpropofol
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Sourcing guidance for Propofol
What are the critical quality standards and certifications required for sourcing Propofol?
As a high-risk pharmaceutical anesthetic, Propofol must strictly adhere to international pharmacopoeia standards such as USP (United States Pharmacopeia), BP (British Pharmacopeia), or EP (European Pharmacopoeia). Buyers must verify that the manufacturer holds a valid GMP (Good Manufacturing Practice) certificate and a Drug Master File (DMF) registration. For cross-border trade, ensure the supplier provides a Certificate of Analysis (COA) for every batch to confirm purity, pH levels, and emulsion stability.
What technical specifications are vital for Propofol emulsions?
Propofol is typically supplied as a 1% (10mg/mL) or 2% (20mg/mL) injectable emulsion. Key technical factors include the lipid emulsion base (usually soybean oil, glycerol, and egg lecithin), which must have a mean particle size of less than 500nm to prevent embolism. Additionally, check if the formulation contains antimicrobial preservatives like EDTA or sodium metabisulfite, as this affects the shelf life and clinical usage protocols.
What are the storage and stability requirements for Propofol during transit?
Propofol is highly sensitive to temperature. It must be stored and transported within a controlled range of 4°C to 25°C (40°F to 77°F). It must not be frozen, as freezing breaks the emulsion, rendering the drug dangerous for use. Suppliers should use validated cold-chain logistics and include temperature data loggers in the packaging to ensure the product's integrity upon arrival.
How can a buyer verify the legitimacy of a pharmaceutical supplier?
Professional B2B buyers should utilize platforms like Made-in-China.com to identify Audited Suppliers. Always request the supplier's Pharmaceutical Manufacturing License and verify their export history. It is highly recommended to conduct a third-party factory audit to inspect the sterile production lines and quality control laboratories before finalizing a large-scale procurement contract.
Cross-Border Procurement Risks and Compliance for Controlled Substances
What are the legal and regulatory risks associated with importing Propofol?
Propofol is a strictly regulated prescription medication and, in many jurisdictions, is classified as a controlled substance due to its potential for misuse. Buyers must possess a Medical Device or Pharmaceutical Import License in their destination country. Failure to provide an Import Permit and the supplier's Export Permit will result in immediate customs seizure and potential legal penalties.
How should payment and transaction security be handled for medical supplies?
To mitigate financial risk, use secure payment terms such as Letter of Credit (L/C) or escrow services provided by reputable platforms like Made-in-China.com. Avoid 100% upfront wire transfers to unknown entities. Ensure the contract includes a quality claim clause that allows for independent lab testing upon receipt before the final payment is released.
What are the specific shipping precautions for liquid pharmaceutical emulsions?
Propofol is usually packaged in glass ampoules or vials, which are fragile. Packaging must include shock-absorbent materials and be labeled as 'Fragile' and 'Keep Upright'. Because it is a liquid chemical, it requires a Material Safety Data Sheet (MSDS) and a Non-Dangerous Goods Certificate (or IMO Declaration if applicable) for air or sea freight clearance.
How can I negotiate better terms with pharmaceutical manufacturers?
Focus on long-term supply stability rather than just the lowest price. Negotiate based on annual volume commitments to secure a lower unit price. Ask for extended shelf-life guarantees (typically 24 months) and ensure the supplier can provide customized labeling and inserts that comply with the language and regulatory requirements of your local Ministry of Health.























