A deep determination to manufacturing top-quality, good quality merchandise and exceptional client satisfaction is our number one precedence. The metering and dispensing methods that Ivek generates present excellent overall performance and reliability for probably the most demanding programs.
A. Aseptic processing is often a manufacturing method that may generate products which is absent of germs without having subjecting the product to terminal sterilization processes. Lots of merchandise degrade and become ineffective when subjected to the harsh conditions of terminal sterilization.
Liquid bottle filling devices supply significant Charge price savings and contribute to squander reduction, building them an invaluable asset in promoting sustainable tactics inside the pharmaceutical market.
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Single Channel IVEK’s precision liquid dispensing rotary methods are capable of dispensing 1uL – 8mL inside a next and run possibly Single-Close or Dual-Conclude Motors giving you (1) or (2) dispenses at a time. Our higher precision liquid dispensing linear units are able to linear move from 2nL – 2mL.
Spray Systems IVEK’s spray units offer many of the smallest and most reliable droplet distributions accessible, masking the widest viscosity ranges during the market. Presents a regular and precise coating.
When developing a sterile products, individuals typically never fully grasp what’s necessary to manufacture the item. Does the molecule need aseptic filling, or can or not it's terminally sterilized? Is the appliance certainly a sterile plan and how do they locate the best CDMO to manufacture their product or service securely and efficiently?
The Biowelder® TC is an automated device for connecting thermoplastic tubing within a sterile welding operation.
The significant space is defined as The situation through which the sterilized drug solution, containers, and closures are subjected to environmental problems that must retain the item's sterility.
But the literature lacks sufficient cases from the implementation of QRM inside the manufacturing stage of sterile products and solutions plus the involved pitfalls of this step.
The chance evaluation method is made get more info up of a few actions. In step one, a listing of probable dangers relevant to the target procedure is ready for hazards to generally be identified, accompanied by risk analysis to higher fully grasp the here threats. The attainable harms with the threats might be measured, regardless of whether qualitatively or quantitatively or at the same time.
The combination of lessened product losses and labour discounts contributes towards the economic viability of pharmaceutical manufacturing. With Improved Value-success, companies can allocate assets strategically, put money into investigate and growth, and deliver impressive products to the marketplace.
A comprehensive portfolio of standard and custom made tube sets for transfer, distribution or filling of in-approach fluids.
Collection of nutrient medium ought to be built depending on dosage sort of the merchandise and selectivity, clarity, focus and suitability for sterilization of nutrient medium.