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SOP for cleaning of Pass Box

  •  Objective
  • To lay down a procedure for cleaning of Pass Box.
  • Scope
  • This SOP is applicable for the procedure of cleaning of Pass Box in the formulation plant of pharmaceutical company.
  • Responsibility
  • Production Operator/ Technician – For the cleaning of the equipment.
  • Production Officer/ Executive– To ensure the cleanliness of the equipment.
  •  Accountability
  • Production Head and QA shall be accountable for the compliance of the SOP.
  • Abbreviations:
  • SOP : Standard Operating Procedure.
  • PRD: Production Department
  • No. : Number.
  • S.S. : Stainless Steel.
  • Procedure
  • Switch OFF main power supply of Machine.
  • Clean the cabinet by using dry lint free duster.
  • Clean the doors and door handle by using dry lint free duster.
  • Clean the S.S. caps by using dry lint free duster.
  • Clean the light diffuser by using dry lint free duster.
  • Wipe the cabinet by using wet lint free duster.
  • Wipe the doors by using wet lint free duster.
  • Wipe the door handles by using wet lint free duster.
  • Wipe the hinges by using wet lint free duster.
  • Clean the cabinet by using dry lint free duster.
  • Clean the doors and door handle by using dry lint free duster.
  • Clean the S.S. caps by using dry lint free duster.
  • Clean the light diffuser by using dry lint free duster.
  •  Affix “CLEANED” label on Pass Box.
  • Forms and Records (Annexures)
  • Not Applicable  
  • Distribution
  • Master copy –   Quality Assurance
  • Controlled copies- Quality Assurance, Production, Quality Control
  • History
    Date Revision Number
    Reason for Revision
    00 New SOP

 

About Pharmaceutical Guidanace

Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 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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