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SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

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Tag: Pharmacovigilance risk management plan SOP

SOP for Pharmacovigilance System Maintenance

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SOP for Pharmacovigilance System Maintenance Guidelines for Pharmacovigilance System Maintenance 1) Purpose The purpose of this SOP is to outline procedures for the ongoing maintenance and support of pharmacovigilance systems to ensure continuous functionality, data integrity, and compliance with regulatory requirements. 2) Scope This SOP applies to personnel responsible for pharmacovigilance system maintenance, including IT…

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Pharmacovigilance

SOP for Pharmacovigilance System Validation

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SOP for Pharmacovigilance System Validation Guidelines for Pharmacovigilance System Validation 1) Purpose The purpose of this SOP is to establish procedures for validating pharmacovigilance systems to ensure compliance with regulatory requirements and data integrity standards. 2) Scope This SOP applies to personnel responsible for pharmacovigilance system validation, including IT personnel, pharmacovigilance managers, and quality assurance…

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Pharmacovigilance

SOP for Pharmacovigilance Safety Database Upgrades

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SOP for Pharmacovigilance Safety Database Upgrades Guidelines for Pharmacovigilance Safety Database Upgrades 1) Purpose The purpose of this SOP is to define procedures for planning, executing, and validating upgrades to the pharmacovigilance safety database to enhance functionality, performance, and compliance. 2) Scope This SOP applies to personnel responsible for pharmacovigilance database management, including database administrators…

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Pharmacovigilance

SOP for Pharmacovigilance Safety Database Lock Procedures

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SOP for Pharmacovigilance Safety Database Lock Procedures Guidelines for Pharmacovigilance Safety Database Lock Procedures 1) Purpose The purpose of this SOP is to establish procedures for locking the pharmacovigilance safety database at predefined intervals to ensure data integrity and regulatory compliance. 2) Scope This SOP applies to personnel responsible for pharmacovigilance database management, including database…

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Pharmacovigilance

SOP for Pharmacovigilance Aggregate Report Distribution

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SOP for Pharmacovigilance Aggregate Report Distribution Guidelines for Pharmacovigilance Aggregate Report Distribution 1) Purpose The purpose of this SOP is to define procedures for the distribution of pharmacovigilance aggregate reports to regulatory authorities, marketing authorization holders (MAHs), and other stakeholders in compliance with regulatory requirements. 2) Scope This SOP applies to personnel responsible for pharmacovigilance…

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Pharmacovigilance

SOP for Pharmacovigilance Expedited Reporting Criteria

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SOP for Pharmacovigilance Expedited Reporting Criteria Guidelines for Pharmacovigilance Expedited Reporting Criteria 1) Purpose The purpose of this SOP is to establish criteria and procedures for identifying and reporting expedited safety reports of suspected serious adverse reactions (SUSARs) to regulatory authorities within defined timelines. 2) Scope This SOP applies to personnel responsible for pharmacovigilance case…

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Pharmacovigilance

SOP for Pharmacovigilance Causality Assessment

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SOP for Pharmacovigilance Causality Assessment Guidelines for Pharmacovigilance Causality Assessment 1) Purpose The purpose of this SOP is to establish procedures for conducting causality assessment of adverse events reported in pharmacovigilance to determine the likelihood of a causal relationship between medicinal products and adverse events. 2) Scope This SOP applies to personnel involved in pharmacovigilance…

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Pharmacovigilance

SOP for Pharmacovigilance Seriousness Assessment

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SOP for Pharmacovigilance Seriousness Assessment Guidelines for Pharmacovigilance Seriousness Assessment 1) Purpose The purpose of this SOP is to provide guidelines for assessing the seriousness of adverse events reported in pharmacovigilance to determine appropriate regulatory reporting and risk management actions. 2) Scope This SOP applies to personnel responsible for pharmacovigilance case assessment and seriousness determination…

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Pharmacovigilance

SOP for Pharmacovigilance Data Analysis and Reporting

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SOP for Pharmacovigilance Data Analysis and Reporting Guidelines for Pharmacovigilance Data Analysis and Reporting 1) Purpose The purpose of this SOP is to establish procedures for conducting pharmacovigilance data analysis and preparing accurate and timely safety reports to regulatory authorities and stakeholders. 2) Scope This SOP applies to personnel involved in pharmacovigilance data analysis, reporting,…

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Pharmacovigilance

SOP for Pharmacovigilance Data Entry and Verification

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SOP for Pharmacovigilance Data Entry and Verification Guidelines for Pharmacovigilance Data Entry and Verification 1) Purpose The purpose of this SOP is to establish standardized procedures for accurate and timely data entry and verification in pharmacovigilance to ensure data quality and compliance with regulatory requirements. 2) Scope This SOP applies to personnel involved in pharmacovigilance…

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Pharmacovigilance

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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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