Meet the Challenges of Biopharmaceutical Powder Manufacture with EZ BioPac®

EZ BioPac® is a single-use powder containment and transfer system, purpose-built by ILC Dover. It is recognized as the fastest and most efficient powder containment and transfer system, speeding fill time and making it easy to adjust contents to precise target weight. Download our information sheet to learn more about the advantages and use-cases for EZ BioPac®.

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Featured! Sentinel Clear XT™ PAPR SystemHow EZ BioPac<sup>®</sup> Works

EZ BioPac® features a separate discharge outlet and antistatic polymer material for faster, cleaner discharge with residuals consistently 2g or less in a 5 kg bag. The bag’s unique design and protective skirt reduce or eliminate contamination of the support stand and bag exterior, drastically reducing clean-up requirements. Its large diameter top-opening permits easy filling and fine-tuning of final weight. It is suitable for a wide range of filling/dispensing volumes, flow rates, and product weights.

Why EZ BioPac® from ILC Dover?

Ease of Use

EZ BioPac® bags and custom polypropylene support stand allow fast, foolproof set-up

Fast Fill Time

Large-diameter top opening speeds filling by as much as 71%

Less Cleaning

Attached zip ties or ILC Dover’s proprietary crimping system assure complete closure and containment

Wide Capacity Range

Bags are available in capacities from 1-to-100 liters to suit full range of plant requirements

Array of Flange Sizes

Discharge sanitary flange sizes range from 1.5˝ to 8˝ to match a variety of process vessels

The Benefits of EZ BioPac®

Unlike systems adapted from an existing liquid-handling system, EZ BioPac® is designed specifically to handle powders in biopharmaceutical applications. It has proven to substantially lessen the amount of powder that disperses into the air, reduces the time needed for changeover, lowers staff costs, and frees staff to work on more vital jobs, which all contribute to profitability.

Certified Quality for GMP

EZ BioPac®’s ArmorFlex film meets FDA and 2002/72/EC requirements and EP 3.1.3 test conditions. It complies with FDA 21 CFR and passes USP <661> Physiochemical Tests for Plastics, USP <88> Class VI (7-day implant), USP <87> biological reactivity (in vitro) and Chilworth incendivity tests. Its permanent antistatic has a five-year shelf life and replaces migrating additives. EZ BioPac® is also tested for solvent resistance, and a DMF has been filed with FDA.