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Immuno TechHorizontal Laminar Flow Cabinets receive their name due to the direction of air flow which comes from above but then changes direction and is processed across the work in a horizontal direction. The constant flow of filtered air provides material and product protection.
We are the main supplier of this product.
Immuno TechPass through box is designed to minimize traffic and contamination entry into the clean room, enables parts, tools and other work items to be passed to and from the room. Unit acts as an air lock device preventing ambient air from entering, exiting the clean room. Dynamic Pass Box allows operation in sterile and particle free conditions because the continuous flushing of the working area by a unidirectional and vertical and ultra filtered airflow, it assures a full product protection.
Technical Specification
The range of Immuno Tech laminar air flow ceilings ensures efficient protection against contamination which can occurduring invasive acts and caused by airborne dead or living particles.
The ceilings are available in square, rectangular, octagonal or circular shapes in order to suit any room layoutand answer specific requirements to create a clean zone around the patient, medical staff and medical devices.Our laminar flow ceilings are mainly used with our Clinicair Air Handling Unit, but can be also adapted to anytype of products from a different brand.
This system is dedicated to operating theatres in order to meet ISO 5 standard (complying withEN ISO 14644-1 ) as well as to pharmaceutical industry. It helps fight cross contamination and hospital borneinfections.
The diffusion plenum is made of 15/10 electro galvanized metal sheet with whiteepoxy paint or stainless steel strictly airtight, and is equipped with air filters of typeH14 (efficiency greater than 99.995% according to EN 1822).It is equipped with an anti-induction lateral apron that enables to eliminate almostcompletely the penetration of airborne particles (in particular via the swivel arms).Possibility to set the speed of air diffusion (from 0.25 to 0.50 m/s) in 2 distinct zones (central and peripheral) which improves the working comfort of medical staff (forlong duration surgeries), reduces the penetration of airborne bio contamination inthe protected area, and enables the evacuation of smokes emitted during surgerie
ImmunotechThe manufacture of oral solid dosage forms such as tablets is a complex multi-stage process under which the starting materials change their physical characteristics a number of times before the final dosage form is produced. Traditionally, tablets have been made by granulation, a process that imparts two primary requisites to formulate: compatibility and fluidity. Both wet granulation and dry granulation (slugging and roll compaction) are used. Regardless of whether tablets are made by direct compression or granulation, the first step, milling and mixing, is the same; subsequent steps differ. Numerous unit processes are involved in making tablets, including particle size reduction and sizing, blending, granulation, drying, compaction, and (frequently) coating. Various factors associated with these processes can seriously affect content uniformity, bioavailability, or stability.
Sampling/Dispensing is the first step in any pharmaceutical manufacturing process. Sampling/Dispensing is one of the most critical steps in pharmaceutical manufacturing; as during this step, the weight of each ingredient in the mixture is determined according to dose. Dispensing may be done by purely manual by hand scooping from primary containers and weighing each ingredient by hand on a weigh scale, manual weighing with material lifting assistance like Vacuum transfer and Bag lifters, manual or assisted transfer with automated weighing on weigh table, manual or assisted filling of loss-in weight dispensing system, automated dispensaries with mechanical devices such as vacuum loading system and screw feed system. Issues like weighing accuracy, dust control (LAF booths, glove boxes), during manual handling, lot control of each ingredient, material movement into and out of dispensary should be considered during dispensing.
ImmunotechThe manufacture of oral solid dosage forms such as tablets is a complex multi-stage process under which the starting materials change their physical characteristics a number of times before the final dosage form is produced. Traditionally, tablets have been made by granulation, a process that imparts two primary requisites to formulate: compatibility and fluidity. Both wet granulation and dry granulation (slugging and roll compaction) are used. Regardless of whether tablets are made by direct compression or granulation, the first step, milling and mixing, is the same; subsequent steps differ. Numerous unit processes are involved in making tablets, including particle size reduction and sizing, blending, granulation, drying, compaction, and (frequently) coating. Various factors associated with these processes can seriously affect content uniformity, bioavailability, or stability.
Sampling/Dispensing is the first step in any pharmaceutical manufacturing process. Sampling/Dispensing is one of the most critical steps in pharmaceutical manufacturing; as during this step, the weight of each ingredient in the mixture is determined according to dose. Dispensing may be done by purely manual by hand scooping from primary containers and weighing each ingredient by hand on a weigh scale, manual weighing with material lifting assistance like Vacuum transfer and Bag lifters, manual or assisted transfer with automated weighing on weigh table, manual or assisted filling of loss-in weight dispensing system, automated dispensaries with mechanical devices such as vacuum loading system and screw feed system. Issues like weighing accuracy, dust control (LAF booths, glove boxes), during manual handling, lot control of each ingredient, material movement into and out of dispensary should be considered during dispensing.