Offer expires September 30

Time left:

DAYS
HOURS
MINUTES
SECONDS

For teams without an in-house WFI still · Made in the USA

Water for Injection USP-Grade Quality
From QC volumes to production scale

Water for Injection quality for pharmaceutical, biotech, CDMO, diagnostics, and medical device teams. Produced under cGMP for research and further manufacturing, with a Certificate of Analysis and volumes from a few litres to 200 L drums.

For research and further manufacturing use only. Not for direct injection, ingestion or inhalation in humans or animals.

See pack sizes & pricing Talk to a WFI specialist
10% OFF First order — use code WELCOME10 at checkout
WFI Quality Water 1L bottles on the filling line at ILC Dover's cGMP facility in Lillington, NC
Produced and filled under validated cGMP conditions in Lillington, NC
ISO 9001:2015 ISO 13485:2016 21 CFR 820 cGMP · FDA Registered ISO 7 Cleanroom Production Tested per USP

Pack sizes & price per litre

Order online with a card, or request a quote for purchase-order and net terms.

SIZE CONTAINER BEST FOR PRICE PER LITRE LEAD TIME
6 × 1 L
 6 × 1 L Bottles, 6 L total Lab, QC, small-batch buffer prep $99.72 $89.75 $16.62 $14.96 3–5 business days
4 × 4 L
 4 × 4 L Jugs, 16 L total Equipment rinse, mid-scale prep $350.36 $315.32 $21.90 $19.71 3–5 business days
10 L
 10 L Single-use bag: 3 port, Luer & MPC connectors, TPE tubing Aseptic transfer into a single-use assembly $330.60 $297.54 $33.06 $29.75 3–5 business days
200 L
 200 L Drum Production-scale buffer & media, CIP $1,299.00 $1,169.10 $6.50 $5.85 BEST VALUE 3–5 business days

Documents

No form. Download what you need directly.

Purified by steam distillation following reverse osmosis and deionisation, with no added substances, the most rigorous WFI route.

Applications

Purified by steam distillation following reverse osmosis and deionisation, with no added substances — the most rigorous WFI route, filled under validated conditions.

2-year shelf life, validated using IPEC Guideline principles. On-site analytical and microbiology testing, with rapid turnaround available.

  • Buffer preparation & buffer exchange
  • Cell culture media preparation
  • High-purity aqueous reagent manufacture
  • Equipment and surface cleaning
  • Analytical testing
  • Final rinse and CIP

Batch release specifications

Every batch is released against these USP limits and shipped with a Certificate of Analysis.

PARAMETER RELEASE LIMIT UNITS USP REFERENCE
Bacterial endotoxin < 0.25 EU/mL USP <85>
Total Organic Carbon (at point of use) ≤ 500 ppb USP <643>
Conductivity Meets specification µS/cm USP <645>
Bioburden ≤ 10 CFU/100 mL USP <61> / <1231>
pH Reported (FIO) pH units USP <791>
Shelf life 2 years from manufacture IPEC stability principles

Speak to someone who can discuss endotoxin limits, validation documentation, purchase-order terms and recurring supply schedules, without being routed through general enquiries.

+1 469 822 8981 customer_service@ilcdover.com