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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 database administrators, data entry operators, and safety specialists.

3) Responsibilities

The Database Management Team is responsible for maintaining the pharmacovigilance database. The Pharmacovigilance (PV) Manager oversees the process to ensure compliance with regulatory requirements and internal standards.

4) Procedure

4.1 Database Setup

  1. Configure the database according to the organization’s requirements and regulatory guidelines.
  2. Ensure proper access controls are in place to restrict unauthorized access.
  3. Implement data encryption to protect sensitive information.
See also  SOP for Pharmacovigilance Medical Dictionary for Regulatory Activities (MedDRA) Coding

4.2 Data Entry and Maintenance

  1. Enter data accurately and completely into the database using standardized forms.
  2. Regularly update the database with new information and corrections.
  3. Perform routine maintenance to ensure optimal database performance.

4.3 Data Backup and Recovery

  1. Establish a regular schedule for database backups to prevent data loss.
  2. Store backup copies in a secure, offsite location.
  3. Test data recovery procedures periodically to ensure they work effectively.

4.4 Data Security

  1. Implement robust security measures to protect the database from unauthorized access and cyber threats.
  2. Regularly update security protocols and software to address emerging threats.
  3. Monitor database access logs
to detect and respond to any suspicious activities.

4.5 Data Integrity and Validation

  1. Conduct regular data integrity checks to identify and correct any discrepancies.
  2. Validate data entries against source documents to ensure accuracy.
  3. Document all validation activities and any corrections made.

4.6 Documentation and Record Keeping

  1. Maintain detailed records of all database management activities, including setup, maintenance, and backups.
  2. Ensure all documentation is securely stored and easily accessible for audits and inspections.
  3. Keep a log of all data corrections and updates made during the validation process.

4.7 Communication

  1. Communicate database management procedures and updates to all relevant staff members.
  2. Provide training on database management tools and methods to ensure consistency and accuracy.
  3. Report any issues or challenges encountered during database management to the PV Manager.

5) Abbreviations, if any

PV – Pharmacovigilance

6) Documents, if any

Database configuration files, data entry forms, backup logs, validation reports.

7) Reference, if any

ICH E2E Pharmacovigilance Planning, EU Good Pharmacovigilance Practices (GVP) Module VI.

8) SOP Version

Version 1.0

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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
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  • Injectables
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  • Maintenance Dept.
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  • Microbiology Testing
  • Nanoparticle Formulation
  • Nasal Spray Formulations
  • Nebulizers
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  • Pharmacovigilance
  • Powder & Granules
  • Purchase Departments
  • Quality Assurance
  • Quality Control
  • Raw Material Stores
  • Regulatory Affairs
  • Tablet Manufacturing
  • Rectal Dosage Forms
  • Transdermal Patches
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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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