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6 Results Found

  • Article
  • Open Access
4,465 Views
16 Pages

25 April 2024

Even though, nowadays, most medicines are manufactured industrially, patients may have medical needs that can only be met by a tailor-made approach. This requires the availability of pharmacy preparations made under Good Manufacturing Practice (GMP)...

  • Article
  • Open Access
13 Citations
5,705 Views
11 Pages

Aims: Aim of this study was to monitor the environment at the Transplant Unit—Hemato-Oncology Clinic, University Hospital Olomouc (Olomouc, Czech Republic) and identify risks for the patients. Methods and Results: Microorganisms were cultivated under...

  • Article
  • Open Access
1,795 Views
25 Pages

Impact of Airflow Disturbance from Human Motion on Contaminant Control in Cleanroom Environments: A CFD-Based Analysis

  • Abiyeva Guldana,
  • Sayat Niyetbay,
  • Arman Zhanguzhinov,
  • Gulbanu Kassabekova,
  • Dilyara Jartayeva,
  • Kulyash Alimova,
  • Gulnaz Zhakapbayeva and
  • Khalkhabay Bostandyk

27 June 2025

The growing demands for sanitary regulations in medical facilities, particularly operating rooms, highlight the importance of ensuring high air quality and minimizing airborne hospital-acquired infections. Improperly designed ventilation systems may...

  • Article
  • Open Access
4 Citations
4,553 Views
16 Pages

Design and Construction of a Radiochemistry Laboratory and cGMP-Compliant Radiopharmacy Facility

  • Angela Asor,
  • Abdullah Metebi,
  • Kylie Smith,
  • Kurt Last,
  • Elaine Strauss and
  • Jinda Fan

The establishment of a compliant radiopharmacy facility within a university setting is crucial for supporting fundamental and preclinical studies, as well as for the production of high-quality radiopharmaceuticals for clinical testing in human protoc...

  • Article
  • Open Access
946 Views
15 Pages

8 August 2025

Maintaining air quality in operating rooms is critical for infection control and patient safety. Particulate matter, originating from surgical instruments, personnel, and external sources, is influenced by airflow patterns and ventilation efficiency....

  • Article
  • Open Access

Validation of the Qualified Air System in the Pharmaceutical Industry

  • Ignacio Emilio Chica Arrieta,
  • Vladimir Llinás Chica,
  • Angela Patricia González Parias,
  • Ainhoa Rubio-Clemente and
  • Edwin Chica
Sci2026, 8(2), 25;https://doi.org/10.3390/sci8020025 
(registering DOI)

24 January 2026

The present study describes the ten-year (2014–2024) validation of a Class 100,000ISO 8 qualified air system used in the manufacture of non-sterile pharmaceutical dosage forms in a GMP-certified facility. The lifecycle evaluation included desig...