JS Pharmatechno Services
JS Pharmatechno are one of the manufacturers of HVAC Clean Room projects and Turnkey Solution Provider within India. We provide cost-effective Enterprise Solutions & Turn-Key services customized for specific projects and typical requirements
Projects
We are determined to meet high moral and ethical standards in performing our work at every level of our organization and in every location where we operate.
HVAC CLEAN ROOM
We, at JS Pharmatechno, understand that appropriate sizing of HVAC components is critical for the design of energy-efficient HVAC systems at optimum cost.
TURNKEY
We take into consideration various factors such as climate, building configuration, space usage, System & Area zoning, and classifications.
CUSTOMIZED PROJECTS
We have experienced architects, engineers, developers, plant managers, etc to deliver the highest quality product within specifications and on schedule.
Why Choose JS Pharma?
We provide cost-effective Enterprise Solutions & Turn-Key services customized for specific projects and typical requirements.
We believe that progress must be achieved in harmony with the environment.
A commitment to environmental protection is an integral part of the corporate vision.
Trusted
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Performance and leadership into JS Pharmatechno personnel.
Key Essentials
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Genuine Quality, Dedication, Responsibility, Respect, and Determination
Legacy
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Assuming responsibility, and acting with respect and determination.
Future
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To nurture our technology leadership, our pioneering spirit, and ability to be “at home” everywhere
CALIBRATION AND VALIDATION
JS Pharmatechno consists a team of Experienced and Qualified CALIBRATION and VALIDATION SPECIALISTS in the field of Pharmaceuticals, API factory, Clinical-Research, R&D, Quality Control Laboratories, Hospitals etc.
Cleanroom Validation with accurate documentation of paramount importance. A well-conceived properly administered maintenance program can be measured by regular testing of the facility by our technicians. A Program of periodic inspection can be established on a Quarterly, Half Yearly or Annual basis. Once a program has been initiated, the schedules of onsite testing will be accomplished automatically. We execute the Cleanroom Validation requirements.
Equipment and Process Validation is done by keeping in mind about the critical requirements of various regulatory authorities and Latest GMP, GLP requirements in the industry.
Now international standard impactor mensuration service now available in India with minimum turnaround time.