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SOP for Personnel Hygiene and Gowning

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SOP for Personnel Hygiene and Gowning

Standard Operating Procedure for Personnel Hygiene and Gowning in Otic Manufacturing Unit

1) Purpose

To ensure that personnel maintain high standards of hygiene and gowning practices to prevent contamination during manufacturing of Otic (Ear) Dosage Forms.

2) Scope

This SOP applies to all personnel entering manufacturing areas where Otic dosage forms are processed, including production, quality control, and maintenance staff.

3) Responsibilities

Operators: Responsible for following gowning procedures and maintaining personal hygiene.
Supervisors: Responsible for ensuring compliance with gowning requirements.
Quality Assurance: Responsible for monitoring and auditing gowning practices.

See also  SOP for Vacuum Oven

4) Procedure

4.1 General Hygiene Requirements
4.1.1 Hand Washing
4.1.1.1 Wash hands thoroughly with soap and water before entering production areas.
4.1.1.2 Use hand sanitizers as per defined protocols.

4.1.2 Personal Protective Equipment (PPE)
4.1.2.1 Wear appropriate PPE including clean uniforms, hairnets, masks, and gloves.
4.1.2.2 Change PPE as required or when contamination is suspected.

4.2 Gowning Procedure
4.2.1 Gowning Area
4.2.1.1 Enter the designated gowning area.
4.2.1.2 Ensure the gowning area is clean and free from contaminants.

4.2.2 Gowning Steps

4.2.2.1 Don gown in the following order: coveralls, hair covers, face masks, and shoe covers.
4.2.2.2 Ensure all gowning steps are followed meticulously to prevent contamination.

See also  SOP for Weighing Balance

4.3 Behavior in Manufacturing Areas
4.3.1 Conduct
4.3.1.1 Avoid unnecessary movements and activities that may compromise hygiene.
4.3.1.2 Report any breaches in hygiene practices immediately to supervisors.

5) Abbreviations, if any

PPE: Personal Protective Equipment
SOP: Standard Operating Procedure

6) Documents, if any

Gowning log
Training records for hygiene practices

7) Reference, if any

GMP guidelines for personnel hygiene in pharmaceutical manufacturing

8) SOP Version

Version 1.0

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Standard Operating Procedures V 1.0

  • Aerosols
  • Analytical Method Development
  • Bioequivalence Bioavailability Study
  • Capsule Formulation
  • Clinical Studies
  • Creams
  • Data Integrity
  • Dental Dosage Forms
  • Drug Discovery
  • Environment, Health and Safety
  • Formulation Development
  • Gels
  • Good Distribution Practice
  • Good Warehousing Practices
  • In-Process Control
  • Injectables
  • Liquid Orals
  • Liposome and Emulsion Formulations
  • Lotions
  • Lyophilized Products
  • Maintenance Dept.
  • Medical Devices
  • Metered-Dose Inhaler
  • Microbiology Testing
  • Nanoparticle Formulation
  • Nasal Spray Formulations
  • Nebulizers
  • Ocular (Eye) Dosage Forms
  • Ointments
  • Otic (Ear) Dosage Forms
  • Pharmacovigilance
  • Powder & Granules
  • Purchase Departments
  • Quality Assurance
  • Quality Control
  • Raw Material Stores
  • Regulatory Affairs
  • Tablet Manufacturing
  • Rectal Dosage Forms
  • Transdermal Patches
  • Vaginal Dosage Forms
  • Validations and Qualifications

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NEW! Revised SOPs – V 2.0

  • Aerosols V 2.0
  • Analytical Method Development V 2.0
  • API Manufacturing V 2.0
  • BA-BE Studies V 2.0
  • Biosimilars V 2.0
  • Capsules V 2.0
  • Creams V 2.0
  • Elixers V 2.0
  • Ointments V 2.0
  • Raw Material Warehouse V 2.0
  • Tablet Manufacturing V2.0

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