Operating Procedure of Dehumidifier

  • Objective:To lay down an Operating Procedure for Dehumidifier
  • Scope:This Standard Operating Procedure is applicable to the formulation plant of Pharmaceutical Company.
  • Responsibility
    • The Concerned Technician shall follow the Operating Procedure as per this SOP
    • The Officer/Executive-Engineering shall be responsible for implementation of the procedure as per this SOP.
  • Accountability: Head-Engineering and QA shall be accountable for compliance of the procedure as per this SOP.
  • Abbreviations and Definitions:
  • MCC : Machine Control Center
  • MCB : Miniature Circuit Board
  • RH : Relative Humidity
  • Procedure
    • Pre Startup Checkup
      • Ensure Power supply shall “ON” from MCC panel for all deparment
      • Ensure Chilled Water circulation is going on. Working Pressure of Chilled water shall be more than 1 Kg/Cm2.
      • Ensure that steam inlet valve should be open.
      • Ensure that inlet and outlet damper of dehumidifier should be open.
    • Starting Procedure
      • Switch on the MCB from the panel
      • Set the desire Temperature and RH on the temperature and RH controller.
      • Switch “ON” the selector switch, then process and react blower will be on.
      • Switch “ON” the heaters.
      • Ensure that there are no leakages from the door gaskets.
    • Forms and Annexure:
    • Not Applicable
  • Distribution:
    • Master Copy : Documentation Cell
    • Controlled Copies :Engineering, Production, Quality Assurance,Warehouse,Quality control and Administration and House Keeping.
  • History:
Date Revision Number Reason for revision
 – 00 New SOP

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About Pharmaceutical Guidanace

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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