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PRODID:-//CST Validations - ECPv6.15.17.1//NONSGML v1.0//EN
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X-ORIGINAL-URL:https://www.cstvalconsulting.co.za
X-WR-CALDESC:Events for CST Validations
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DTSTART:20250101T000000
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BEGIN:VEVENT
DTSTART;TZID=UTC:20260625T080000
DTEND;TZID=UTC:20260626T170000
DTSTAMP:20260505T090108
CREATED:20260319T124557Z
LAST-MODIFIED:20260319T104217Z
UID:578-1782374400-1782493200@www.cstvalconsulting.co.za
SUMMARY:PHARMACEUTICAL UTILITIES (HVAC\, WATER\, COMPRESSED AIR\, NITROGEN\, STEAM)
DESCRIPTION:This 2-day intensive course covers critical pharmaceutical utility systems that are important for proper functionality\, compliance and efficiency of manufacturing facilities. \nWhat You’ll Learn:\nParticipants will gain practical insights into key systems such as:\n– Water: Potable Water\, Purified Water\, Water for Injection (WFI)\n– Steam: Plant Steam\, Industrial Steam\, Pure Steam/Clean Steam\n– Gases: Compressed Air\, Nitrogen\, Process Gases  \n\n\nIndustry best practices for commissioning and qualification of pharmaceutical water and steam systems \n\n\nEffective sampling techniques for water\, steam\, and process gases \n\n\nControl strategies for maintaining system integrity and preventing contamination \n\n\nApplication of HVAC systems in both sterile and non-sterile environments \n\n\nKey considerations for: \n\n\nOral solid dosage manufacturing \n\n\nSterile product manufacturing facilities \n\n\n\n\nGuidelines & References\nThis course is aligned with globally recognized regulatory guidelines and references including:\n– ISPE Baseline Guide – Water and steam systems\n– PIC/S Guideline\,\n– WHO Guidelines and Technical Reports\n– ISO 14644\,\n– BP and Phar. Eur.\n– USP\n– PDA Technical Reports & ISO 22519 \n-EMA/INS/GMP/443117/2020 (revised): Q&A on production of water for injections by non-distillation methods – reverse osmosis and biofilms and control strategies\nEMA/CHMP/CVMP/QWP496873/2018 (revised): Guideline on the quality of water for pharmaceutical use\n– EU GMP Annex 1 (revised): Safety and quality in sterile product manufacturing \nWhat You’ll Walk Away With\nThis training equips your team with the knowledge to prevent contamination risks\, ensure regulatory readiness\, and maintain consistent product quality.
URL:https://www.cstvalconsulting.co.za/event/pharmaceutical-utilities-hvac-water-compressed-air-nitrogen-steam/
LOCATION:Protea Hotel Johannesburg Balalaika Sandton\, Johannesburg\, South Africa
CATEGORIES:CSTVAL
ATTACH;FMTTYPE=image/jpeg:https://www.cstvalconsulting.co.za/wp-content/uploads/2024/02/cisti-mediji.jpg
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BEGIN:VEVENT
DTSTART;TZID=UTC:20260806T080000
DTEND;TZID=UTC:20260807T170000
DTSTAMP:20260505T090108
CREATED:20250129T064224Z
LAST-MODIFIED:20260429T162041Z
UID:570-1786003200-1786122000@www.cstvalconsulting.co.za
SUMMARY:WAREHOUSE GMP\, GWP\, GDP\, GSP REQUIREMENT & QUALIFICATION PROCESS
DESCRIPTION:This practical training equips you with the knowledge and tools to run a fully compliant pharmaceutical warehouse with confidence. \nYou’ll gain clear\, actionable insight into GMP\, GDP\, and GSP\, along with the qualification of warehouse systems\, equipment\, and processes. The course also covers temperature and humidity mapping\, enabling you to meet strict regulatory requirements and avoid costly compliance failures. \nLearn how to design and manage warehouse operations that protect product quality\, pass audits\, and meet global standards\, aligned with PIC/S\, WHO\, FDA\, and SAHPRA. \nWalk away ready to implement what you’ve learned immediately.
URL:https://www.cstvalconsulting.co.za/event/warehouse-gmp-gwp-gdp-gsp-requirement-qualification-process/
LOCATION:Protea Hotel Johannesburg Balalaika Sandton\, Johannesburg\, South Africa
CATEGORIES:CSTVAL
ATTACH;FMTTYPE=image/webp:https://www.cstvalconsulting.co.za/wp-content/uploads/2024/02/what-is-a-warehouse.webp
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BEGIN:VEVENT
DTSTART;TZID=UTC:20260903T080000
DTEND;TZID=UTC:20260904T170000
DTSTAMP:20260505T090108
CREATED:20250129T064730Z
LAST-MODIFIED:20260429T161514Z
UID:574-1788422400-1788541200@www.cstvalconsulting.co.za
SUMMARY:ANALYTICAL INSTRUMENT QUALIFICATION AND COMPUTER SYSTEM VALIDATION
DESCRIPTION:Regulators are tightening their focus on equipment qualification\, computer system validation\, and data integrity—and many companies are still getting it wrong. \nThis intensive 2-day course gives you a clear\, practical roadmap to ensure your analytical equipment and computer systems are fully compliant and inspection-ready. You’ll learn how to plan\, execute\, and document qualification\, calibration\, and validation processes with confidence. \nThe training also breaks down critical regulatory requirements\, including 21 CFR Part 11\, EU GMP Annex 11\, and global data integrity guidelines\, so you understand exactly what inspectors expect. \nThrough real-world examples and interactive exercises\, you’ll develop a risk-based approach to compliance\, helping you avoid costly errors\, warning letters\, and enforcement actions.\nBe ready to implement compliant systems that stand up to regulatory scrutiny.
URL:https://www.cstvalconsulting.co.za/event/analytical-instrument-qualification-and-computer-system-validation/
LOCATION:Protea Hotel Johannesburg Balalaika Sandton\, Johannesburg\, South Africa
CATEGORIES:CSTVAL
ATTACH;FMTTYPE=image/jpeg:https://www.cstvalconsulting.co.za/wp-content/uploads/2024/02/How-to-Become-a-Pharmaceutical-Scientist.jpg
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