A deep commitment to manufacturing exceptional, quality products and solutions and excellent consumer fulfillment is our number 1 priority. The metering and dispensing methods that Ivek creates offer outstanding efficiency and dependability for quite possibly the most demanding applications.
Materials of development for all factors, notably all Get hold of components, for instance device pipe function; inside factors of purchased fittings like automatic valves like elastomeric and mechanical seals; pipeline joint seals; welding materials; filters and filter housings such as casing and substrate levels of cartridges, along with the most important medium and all elastomeric seals; and polymer extrusion gear.
Liquid bottle filling equipment offer major cost price savings and contribute to waste reduction, earning them an priceless asset in advertising and marketing sustainable procedures throughout the pharmaceutical field.
Following your pilot operate, you’ll have item and creation information that could go away a optimistic impact within your brand with investors, distributors, and merchants.
Many drug products which require aseptic fill complete are liquids geared up in a solution or possibly a suspension, such as the pursuing:
IVEK delivers free of charge in-depth analysis to ascertain probably the most appropriate fluid handling process for your personal application.
When acquiring a sterile product, individuals normally don't comprehend what’s required to manufacture the item. Does the molecule need aseptic filling, or can it be terminally sterilized? Is the application truly a sterile software And just how do they uncover the ideal CDMO to manufacture their product or service securely and efficiently?
Safeguarding public health and fitness is of paramount significance within the pharmaceutical industry, and compliance with stringent polices is a essential aspect of obtaining this target. Liquid bottle filling machines Enjoy a pivotal role in guaranteeing adherence to these polices.
Terminal sterilization consists of filling and sealing containers below particular environmental conditions to stop the website contamination of such products and solutions from microbial and particulate subject.
For items that can’t endure terminal sterilization, companies employ aseptic manufacturing. The aseptic manufacturing method demands the drug merchandise and any excipients, the container, as well as stoppers for being separately sterilized prior to staying introduced in to the cleanroom or sterile manufacturing Main exactly where the final product or service is manufactured within a really controlled natural environment continuously monitored for air good quality and opportunity microbial ingress.
Mycap® assemblies are well-suited to most biopharma, vaccine or cell and gene therapy purposes where closed, aseptic fluid managing is required. Check out beneath to read more learn more about the focused apps for Mycap® single-use assemblies.
Set up on an array of tube supplies, Quickseal® gives trustworthy and rapid aseptic tube disconnection.
Opta® SFT aseptic tube connectors make it possible for quick and trustworthy sterile connection and fluid transfer among two pre-sterilized process parts.
Absolutely automatic, semi-automated and manual inspection; plunger rod insertion; automatic business labeling; 2nd info matrix verification; variable print info