In the world of pharmaceuticals, precision is not optional; it’s, in fact, the only option. Even a tiny contaminant can make the medicine less effective. Pharma output comes in several forms, including sterile injectables, oral tablets, and vaccines. All of these call for uncompromising environmental control across every step of the manufacturing process.
For pharma companies with high standards, Kaizen Airtreat provides Turnkey cleanroom solutions, while upholding the highest global standards, including those under cGMP and ISO classifications. We do so with a complete understanding of the process flows and regulatory compliance in every case.
Cleanrooms with their control over the smallest of particulate matter help ensure the desired hygienic environment during active ingredient mixing that prevents cross-contamination and resultant batch inconsistency.
Cleanrooms help create the much-needed aseptic conditions that are essential for the safe filling of vials, ampoules, and syringes. It thus ensures a marked reduction in risks associated with the making of injectable medicines.
Cleanrooms with humidity and dust control protect granules and tablets from degradation, ensuring uniformity of quality and flow during compression.
Cleanrooms with their control over the smallest of particulate matter help ensure the desired hygienic environment during active ingredient mixing that prevents cross-contamination and resultant batch inconsistency.
Cleanrooms help create the much-needed aseptic conditions that are essential for the safe filling of vials, ampoules, and syringes. It thus ensures a marked reduction in risks associated with the making of injectable medicines.
Cleanrooms with humidity and dust control protect granules and tablets from degradation, ensuring uniformity of quality and flow during compression.
Cleanroom-controlled zones help prevent particulate and microbial contamination during packing, be it blister packing, strip sealing, or secondary packaging.
Cleanrooms with the correct and certified equipment that we specialise in are necessary for clean and calibrated conditions for sampling, analysis, validation, and microbial testing.
Vaccine development and filling always need the right environment provided by a specialised cleanroom with directional airflow, pressure differentials, and temperature regulation to maintain biosafety and compliance during production.
Cleanroom-controlled zones help prevent particulate and microbial contamination during packing, be it blister packing, strip sealing, or secondary packaging.
Cleanrooms with the correct and certified equipment that we specialise in are necessary for clean and calibrated conditions for sampling, analysis, validation, and microbial testing.
Vaccine development and filling always need the right environment provided by a specialised cleanroom with directional airflow, pressure differentials, and temperature regulation to maintain biosafety and compliance during production.
We specialise in providing Turnkey Solutions, including Designing, Engineering, Procurement, Construction, Commissioning, Validation, and FEED services, including operation & maintenance of cleanroom and HVAC systems that cater to diverse industries such as Automotives, EVs, Semiconductors, Pharmaceuticals, Healthcare and Medical, Electronics, Aerospace, and the Food industry.
We specialise in providing Turnkey Solutions, including Designing, Engineering, Procurement, Construction, Commissioning, Validation, and FEED services, including operation & maintenance of cleanroom and HVAC systems that cater to diverse industries such as Automotives, EVs, Semiconductors, Pharmaceuticals, Healthcare and Medical, Electronics, Aerospace, and the Food industry.
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