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

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

SOP for Training Personnel in Granules Production

Posted on By

SOP for Training Personnel in Granules Production

Standard Operating Procedure for Training Personnel in Granules Production

1) Purpose

The purpose of this SOP is to establish procedures for the training of personnel involved in granules production within the pharmaceutical industry to ensure competency, adherence to procedures, and compliance with regulatory requirements.

2) Scope

This SOP applies to all personnel involved in granules production processes within the pharmaceutical manufacturing facility.

3) Responsibilities

Human Resources (HR) Department: Responsible for coordinating and documenting training activities.
Department Managers/Supervisors: Responsible for identifying training needs and ensuring personnel receive appropriate training.
Training Instructors: Responsible for conducting training sessions and assessing trainee competence.

See also  SOP for Preparation of Powders

4) Procedure

  1. Training Needs Assessment:
    1. Identify specific job roles within granules production that require training.
    2. Assess competency gaps and training requirements for each job role.
  2. Training Program Development:
    1. Develop training programs that include theoretical knowledge and practical skills related to granules production.
    2. Ensure training materials are up-to-date and align with current procedures and regulations.
  3. Training Delivery:
    1. Schedule training sessions based on job roles and operational needs.
    2. Conduct training sessions using appropriate methods (e.g., classroom training, on-the-job training).
  4. Assessment and Competency Evaluation:
    1. Assess trainee understanding and competence through written tests, practical assessments, or simulations.
    2. Document assessment results and provide feedback to trainees.
  5. Training Records:
    1. Maintain accurate records of training activities, including attendance sheets, assessment results, and training
evaluations.
  • Review and update training records as necessary.
  • Continued Education and Refresher Training:
    1. Provide ongoing education and refresher training to reinforce knowledge and skills.
    2. Monitor changes in procedures or regulations that may require additional training.
  • 5) Abbreviations, if any

    SOP: Standard Operating Procedure
    GMP: Good Manufacturing Practice
    HR: Human Resources

    6) Documents, if any

    Training Plans, Training Materials, Training Records

    7) Reference, if any

    Regulatory requirements for personnel training in pharmaceutical manufacturing.

    8) SOP Version

    Version 1.0

    See also  SOP for Maintaining Sterility in Powders Production
    Powder & Granules Tags:analytical method development granules, assay of active ingredient granules, bulk density testing granules, contamination prevention powder, documentation in powder manufacturing, equipment cleaning for powders, final product inspection powder, flowability testing powders, formulation development granules, granulation stability testing, granule calibration SOP, granule production procedure, granule quality control SOP, homogeneity testing granules, in-process testing granules, microbial testing powder, particle size distribution powders, pharmaceutical powder handling, powder blending protocol, powder manufacturing SOP, powder packaging guidelines, powder storage conditions, process optimization powders, process validation powders, raw material inspection powders, sample collection for powders, SOP for granulation techniques, sterility in granule production, training SOP for granule production, waste disposal in granule production

    Post navigation

    Previous Post: SOP for Pharmacovigilance Case Triage
    Next Post: SOP for Preventing Contamination in MDI Production

    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