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SOP Guide for Pharma

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Tag: Pharmacovigilance signal detection SOP

SOP for Pharmacovigilance Aggregate Report Writing

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SOP for Pharmacovigilance Aggregate Report Writing Guidelines for Writing Pharmacovigilance Aggregate Reports 1) Purpose The purpose of this SOP is to establish standardized procedures for writing pharmacovigilance aggregate reports to ensure accurate, consistent, and comprehensive documentation of safety data. 2) Scope This SOP applies to all pharmacovigilance personnel involved in the writing and review of…

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Pharmacovigilance

SOP for Pharmacovigilance Periodic Reporting

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SOP for Pharmacovigilance Periodic Reporting Guidelines for Periodic Pharmacovigilance Reporting 1) Purpose The purpose of this SOP is to establish standardized procedures for the preparation and submission of periodic safety reports to regulatory authorities to ensure ongoing assessment of the benefit-risk profile of medicinal products. 2) Scope This SOP applies to all pharmacovigilance personnel involved…

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Pharmacovigilance

SOP for Pharmacovigilance Expedited Reporting

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SOP for Pharmacovigilance Expedited Reporting Guidelines for Expedited Pharmacovigilance Reporting 1) Purpose The purpose of this SOP is to establish standardized procedures for expedited reporting of serious adverse events (SAEs) to regulatory authorities to ensure timely communication and compliance with regulatory requirements. 2) Scope This SOP applies to all pharmacovigilance personnel involved in the reporting…

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Pharmacovigilance

SOP for Pharmacovigilance Data Entry

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SOP for Pharmacovigilance Data Entry Guidelines for Entering Pharmacovigilance Data 1) Purpose The purpose of this SOP is to establish standardized procedures for entering pharmacovigilance data to ensure accuracy, consistency, and completeness in the pharmacovigilance database. 2) Scope This SOP applies to all pharmacovigilance personnel involved in data entry activities, including data entry operators, safety…

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Pharmacovigilance

SOP for Pharmacovigilance Follow-up Procedures

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SOP for Pharmacovigilance Follow-up Procedures Guidelines for Pharmacovigilance Follow-up Procedures 1) Purpose The purpose of this SOP is to establish standardized procedures for conducting follow-up activities for pharmacovigilance cases to ensure comprehensive data collection and accurate case assessment. 2) Scope This SOP applies to all pharmacovigilance personnel involved in follow-up activities, including safety specialists, case…

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Pharmacovigilance

SOP for Pharmacovigilance Case Narrative Writing

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SOP for Pharmacovigilance Case Narrative Writing Guidelines for Writing Pharmacovigilance Case Narratives 1) Purpose The purpose of this SOP is to establish standardized procedures for writing case narratives in pharmacovigilance to ensure clear, concise, and accurate documentation of adverse event reports. 2) Scope This SOP applies to all pharmacovigilance personnel involved in writing case narratives,…

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Pharmacovigilance

SOP for Pharmacovigilance Case Assessment

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SOP for Pharmacovigilance Case Assessment Guidelines for Assessing Pharmacovigilance Cases 1) Purpose The purpose of this SOP is to establish procedures for the assessment of pharmacovigilance cases to ensure accurate evaluation of adverse event reports and other safety information. 2) Scope This SOP applies to all pharmacovigilance personnel involved in the assessment of case reports,…

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Pharmacovigilance

SOP for Pharmacovigilance Case Intake

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SOP for Pharmacovigilance Case Intake Guidelines for Intake of Pharmacovigilance Cases 1) Purpose The purpose of this SOP is to establish standardized procedures for the intake of pharmacovigilance cases to ensure timely and accurate initial data capture for adverse event reports and other safety information. 2) Scope This SOP applies to all pharmacovigilance personnel involved…

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Pharmacovigilance

SOP for Pharmacovigilance Case Processing

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SOP for Pharmacovigilance Case Processing Guidelines for Processing Pharmacovigilance Cases 1) Purpose The purpose of this SOP is to define the procedures for processing pharmacovigilance cases to ensure timely and accurate reporting of adverse events and other safety information. 2) Scope This SOP applies to all pharmacovigilance personnel involved in the case processing activities, including…

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Pharmacovigilance

SOP for Pharmacovigilance Database Management

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SOP for Pharmacovigilance Database Management Guidelines for Managing Pharmacovigilance Databases 1) Purpose The purpose of this SOP is to define the procedures for managing pharmacovigilance databases to ensure data integrity, security, and accessibility for safety monitoring and reporting. 2) Scope This SOP applies to all pharmacovigilance personnel involved in the management of safety databases, including…

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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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