QA

Tasks:

One of the most important parts of a pharmaceutical company is the Quality Assurance Department, which has a supervisory role for all units and production processes. The purpose of this unit is to enhance the ability to assess quality in all processes related to the design, production and release of the product. Under management of the Authorized Person, the department is working in the following areas:


Documentation

  • Compilation and collection of documentation with the aim of completing and updating documentation on quality assurance and all production-related processes.
  • Compilation and review of documentation related to pharmaceutical processes.
  • Updating the information contained in brochures and artworks and keeping up with the latest standards.
  • Comprehensive drug file preparation in CTD format

  • Validation

    VMP or validation of all processes related to the manufacture of pharmaceutical products.

    Legal affairs and drug registration

  • Completion and tracking of pharmaceutical products and renewal of pharmaceutical permits.
  • Updating the quality parameters of the company products based on new standards and improving their quality.

  • Inspection and GMP

  • Self-assessment of production processes, laboratories and warehouses periodically and determine their compliance with internationally valid principles.
  • Holding GMP training courses