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PRODID:-//CST Validations - ECPv6.15.17.1//NONSGML v1.0//EN
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METHOD:PUBLISH
X-ORIGINAL-URL:https://www.cstvalconsulting.co.za
X-WR-CALDESC:Events for CST Validations
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TZID:UTC
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TZOFFSETFROM:+0000
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DTSTART:20250101T000000
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BEGIN:VEVENT
DTSTART;TZID=UTC:20260806T080000
DTEND;TZID=UTC:20260807T170000
DTSTAMP:20260519T111844
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:20260519T111844
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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