Skip to content
  • Clinical Studies
  • Pharma GMP
  • Pharma Tips
  • Stability Studies
  • Pharma Books
  • Schedule M

SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

  • Home
  • Job Safety Analysis (JSA)
    • Oral Dosage Forms (Tablets & Capsules)
    • Oral Liquid Dosage Forms (Syrups, Elixirs, Suspensions, Emulsions)
    • Powder and Granule Dosage Forms
    • Topical Dosage Forms (Creams, Ointments, Gels, Lotions, Pastes)
    • Transdermal Dosage Forms (Patches)
  • Standard Test Procedures (STP)
  • SOP – Blog Post
  • Toggle search form

Elixir Department: SOP for Use of Personal Protective Equipment (PPE) in Dispensing Room – V 2.0

Posted on By

Elixir Department: SOP for Use of Personal Protective Equipment (PPE) in Dispensing Room – V 2.0

Standard Operating Procedure for Use of Personal Protective Equipment (PPE) in Dispensing Room

Department Elixir Department
SOP No. SOP/ELX/010/2025
Supersedes SOP/ELX/010/2022
Page No. Page 1 of 8
Issue Date 13/04/2025
Effective Date 15/04/2025
Review Date 13/04/2026

1. Purpose

To establish standard requirements and procedures for the appropriate selection, usage, and disposal of personal protective equipment (PPE) by all personnel entering and working in the dispensing room of the Elixir Department.

2. Scope

This SOP applies to all employees, including permanent, temporary, and contract staff, involved in raw material dispensing activities for elixir manufacturing within the designated dispensing area.

3. Responsibilities

  • All Dispensing Personnel:
    • Wear complete PPE before entering the dispensing room.
    • Follow gowning procedure as per training.
  • Warehouse Supervisor:
    • Ensure availability and condition of PPE supplies.
  • Quality Assurance (QA):
    • Conduct audits to verify compliance with PPE usage.
See also  Elixir Department: SOP for Storage of Raw Materials for Elixir Manufacturing - V 2.0

4. Accountability

The Head of Production and the Head of Quality Assurance are jointly accountable for enforcement and monitoring of PPE compliance in the dispensing room.

5. Procedure

5.1 PPE Requirements

  1. The following PPE must be worn before entering the dispensing area:
    • Cleanroom coverall (non-shedding, full body)
    • Head cap
    • Face mask (surgical or N95, depending on sensitivity)
    • Sterile gloves (powder-free)
    • Shoe covers
    • Protective goggles (for handling potent or hazardous materials)
  2. Use disposable PPE wherever applicable; discard after each shift or when soiled.

5.2 Gowning Procedure

  1. Enter the change room adjacent to the dispensing room.
  2. Wear garments in the following order:
    • Head cap
    • Face mask
    • Coverall suit
    • Shoe covers
    • Gloves
    • Goggles
  3. Inspect PPE for damage or contamination before use.
  4. Sanitize gloved hands using 70% IPA before entry.
See also  Elixir Department: SOP for Dispensing Active Pharmaceutical Ingredients for Elixirs - V 2.0

5.3 Rules While Wearing PPE

  1. Do not touch face or mask once PPE is worn.
  2. Do not carry mobile phones, notebooks, or personal items inside the dispensing area.
  3. Immediately replace PPE if it becomes torn, wet, or contaminated.

5.4 Exit Procedure

  1. On completing dispensing activities:
    • Remove PPE in reverse order in the exit change room.
    • Discard disposable items in designated biohazard bins.
    • Place reusable PPE (if any) in the soiled garment bin for laundering.
  2. Sanitize hands and sign the PPE Usage Log (Annexure-1).

5.5 Training and Compliance

  1. All personnel must be trained on gowning procedure annually.
  2. Gowning procedure posters should be displayed at entry points.
  3. QA shall periodically verify PPE compliance and record observations.

6. Abbreviations

  • SOP: Standard Operating Procedure
  • PPE: Personal Protective Equipment
  • IPA: Isopropyl Alcohol
  • QA: Quality Assurance
See also  Elixir Department: SOP for Handling Material Return Post Dispensing - V 2.0

7. Documents

  1. PPE Usage Log (Annexure-1)
  2. Training Record for PPE

8. References

  • WHO GMP Guidelines – Personal Hygiene and Protective Equipment
  • 21 CFR Part 211 – Subpart E: Control of Components and Drug Product Containers

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: PPE Usage Log

Date Employee Name PPE Worn Time In Time Out Remarks
13/04/2025 Rajesh Kumar Coverall, Mask, Gloves, Goggles 09:15 11:30 —

Revision History:

Revision Date Revision No. Revision Details Reason for Revision Approved By
10/01/2022 1.0 Initial Version New SOP QA Head
13/04/2025 2.0 Added exit procedure and reusable PPE control Regulatory Compliance QA Head
Elixers V 2.0 Tags:Elixir colorants, Elixir dosage form, Elixir filtration techniques, Elixir flavoring agents, Elixir formulation, Elixir GMP compliance, Elixir manufacturing process, Elixir manufacturing SOPs, Elixir packaging requirements, Elixir pharmacopoeial standards, Elixir preparation methods, Elixir preservatives, Elixir production equipment, Elixir quality control, Elixir regulatory guidelines, Elixir shelf life, Elixir stability testing, Elixir sterilization methods, Elixir storage conditions, Elixir sweetening agents, Elixir viscosity modifiers, Hydroalcoholic solutions, Medicated elixirs, Non-medicated elixirs, Pharmaceutical elixirs

Post navigation

Previous Post: BA-BE Studies: SOP for Sample Storage at -20°C and -70°C – V 2.0
Next Post: Biosimilars: SOP for mRNA Transcript Analysis (RT-PCR) – V 2.0

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

Read SOPs in your Language:

 - 
Bengali
 - 
bn
English
 - 
en
Gujarati
 - 
gu
Hindi
 - 
hi
Malayalam
 - 
ml
Marathi
 - 
mr
Punjabi
 - 
pa
Tamil
 - 
ta
Telugu
 - 
te

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

New Publication: A must for All.

Copyright © 2025 SOP Guide for Pharma.

Powered by PressBook WordPress theme

Go to mobile version