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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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SOPs for Medical Devices

SOP for Calibration of Quality Testing Equipment

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SOP for Calibration of Quality Testing Equipment Comprehensive Guide to Calibration of Quality Testing Equipment in Medical Device Manufacturing 1) Purpose The purpose of this SOP is to establish a systematic procedure for calibrating quality testing equipment used in medical device manufacturing. Proper calibration ensures accurate, reliable measurements, compliance with regulatory standards, and the production…

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Medical Devices

SOP for Managing Device Master Records (DMR)

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SOP for Managing Device Master Records (DMR) Comprehensive Guide to Managing Device Master Records (DMR) in Medical Device Manufacturing 1) Purpose The purpose of this SOP is to establish a standardized approach to creating, maintaining, and managing Device Master Records (DMR) for medical devices. The DMR is a comprehensive document that defines the specifications, production…

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Medical Devices

SOP for Final Quality Inspection of Medical Devices

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SOP for Final Quality Inspection of Medical Devices Comprehensive Guide to Final Quality Inspection of Medical Devices 1) Purpose The purpose of this SOP is to define a standardized procedure for conducting final quality inspections on medical devices before their release for distribution. This ensures that the devices meet the required quality, safety, and performance…

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Medical Devices

SOP for In-Process Quality Control Checks

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SOP for In-Process Quality Control Checks Comprehensive Guide to In-Process Quality Control Checks in Medical Device Manufacturing 1) Purpose The purpose of this SOP is to establish a systematic procedure for performing in-process quality control (IPQC) checks during the manufacturing of medical devices. These checks ensure that products meet specified standards and regulatory requirements at…

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Medical Devices

SOP for Quality Control Testing of Raw Materials

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SOP for Quality Control Testing of Raw Materials Comprehensive Guide to Quality Control Testing of Raw Materials in Medical Device Manufacturing 1) Purpose The purpose of this SOP is to establish a standardized procedure for testing raw materials used in medical device manufacturing. This ensures that all materials meet the required specifications, quality standards, and…

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Medical Devices

SOP for Disposal of Rejected or Scrap Materials

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SOP for Disposal of Rejected or Scrap Materials Comprehensive Guide to Disposal of Rejected or Scrap Materials in Medical Device Manufacturing 1) Purpose The purpose of this SOP is to define the procedures for handling, documenting, and disposing of rejected or scrap materials in medical device manufacturing. This ensures compliance with environmental regulations, prevents unauthorized…

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Medical Devices

SOP for Handling Non-Conforming Products in Manufacturing

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SOP for Handling Non-Conforming Products in Manufacturing Comprehensive Guide to Handling Non-Conforming Products in Medical Device Manufacturing 1) Purpose The purpose of this SOP is to establish a standardized procedure for identifying, documenting, and handling non-conforming products in the manufacturing process. This ensures that all non-conforming products are managed in a way that maintains compliance…

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Medical Devices

SOP for Tool and Die Maintenance in Medical Device Manufacturing

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SOP for Tool and Die Maintenance in Medical Device Manufacturing Comprehensive Guide to Tool and Die Maintenance in Medical Device Manufacturing 1) Purpose The purpose of this SOP is to define the procedures for maintaining tools and dies used in medical device manufacturing. Proper maintenance ensures precision, prolongs the lifespan of tools and dies, and…

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Medical Devices

SOP for Production Planning and Scheduling

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SOP for Production Planning and Scheduling Comprehensive Guide to Production Planning and Scheduling in Medical Device Manufacturing 1) Purpose The purpose of this SOP is to establish a structured approach to production planning and scheduling in medical device manufacturing. This ensures optimal resource utilization, timely delivery of products, compliance with regulatory standards, and alignment with…

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Medical Devices

SOP for Identifying and Mitigating Manufacturing Risks

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SOP for Identifying and Mitigating Manufacturing Risks Comprehensive Guide to Identifying and Mitigating Manufacturing Risks in Medical Device Production 1) Purpose The purpose of this SOP is to outline a systematic approach for identifying, assessing, and mitigating risks in the manufacturing process of medical devices. This ensures compliance with regulatory standards, maintains product quality, and…

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Medical Devices

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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

New Publication: A must for All.

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