admin, Author at Parsan

The Critical Role of Cleanroom

The pharmaceutical, aero space, medical, electronic, high-tech, semiconductor, and many other industries depend on cleanroom technology.  How to control the micro-organism is a key point to maintain the quality in medical or pharmaceuticals which can be performed by cleanroom. For pharmaceutical companies, clean, safe and contaminant-free products are imperative to manufacturing and distributing a viable […]

Clean Room Equipments

A. PASSBOXES: Pass box is clean room equipment used to transfer materials from one device/room to another in a closed environment to avoid human intervention and prevent cross contamination. It is widely used in Pharmaceutical manufacturing facility, hospitals, laboratories etc. There are two types of pass boxes: Static Pass box: Static pass boxes are used […]

Clean room Industry in India – on the path to progress

The cleanroom industry is one of the major industries growing at lightning speed in today’s world. Increasing Global health crisishas made it imperative that the pharmaceutical industry moves at a rapid pace alongside researchers, regulators, and contract research companies to develop a diagnosis, treatment, and vaccines. Cleanroom technologies and services play an important role in […]

clean room Validation

Why regular HVAC/clean room Validation is important statutory requirement in Pharma or medical device Industry?

HVAC/Cleanroom Validation is provided by conducting a series of tests to qualify if a controlled environment is performing in accordance with process requirements and the applicable regulatory guidelines. Process parameters and controls are determined during the validation of any process or system. Only installing HVAC (Heating Ventilation and Air conditioning) system isn’t always completely effective until a […]

HVAC

Why HVAC (Heating, Ventilation, & Air Conditioning) is an important statutory requirement in Pharma or medical device Industry?

Temperature is required to control as effective blending of ingredients in drug manufacturing process may got affected by change in temperature. So that HVAC (Heating, Ventilation, & Air Conditioning) system is installed in Pharmaceutical &Medical device industry in manufacturing, filling & packaging area to control temperature, humidity, air flow and contamination. Nowadays, the importance of […]

Potential Cleanroom Validation Hazards

For maintaining the health and safety and adhering to the high standards of a controlled cleanroom environment requires thorough training and routine testing and inspections because there are many potential hazards in clean rooms. Several common cleanroom validation hazards are listed below: Pass Through Areas –if onehas to bring a lot of equipment and parts […]

  • 1
  • 2