Quality & Productivity

Pharmaceutical Stability Testing: ICH Study Design, Shelf-Life Statistics and OOT Control – Jeddah, 18–22 Jul 2027

Pharmaceutical Stability Testing: ICH Study Design, Shelf-Life Statistics and OOT Control runs in Jeddah from Sunday 18 July to Thursday 22 July 2027 (1 Week). The fee is 19,500 SAR per participant. The same programme is also scheduled in 7 other cities.

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Dates
Length
1 Week
Fee per participant
19,500 SAR
Format
In person, Jeddah
Venue
Corniche four-star
Status
Open for registration
Week
28 of 2027
Reference
382_15777

This session

18–22 Jul 2027

This Pharmaceutical Stability Testing: ICH Study Design, Shelf-Life Statistics and OOT Control session in Jeddah runs from Sunday 18 July to Thursday 22 July 2027 (week 28, Q3 2027). It is the only date in Jeddah in 2027, at a fee of 19,500 SAR. Registration is open for this date. It is held in person at Corniche four-star.

How do I book this date?

Register online to request your place, or send us a question about this date first.

Reference for this date: 382_15777. Quote it when you contact us.

Before you book, read our cancellation policy.

Let’s talk about your next step.

Questions about this date

When does Pharmaceutical Stability Testing: ICH Study Design, Shelf-Life Statistics and OOT Control in Jeddah start and finish?

It starts on Sunday 18 July and finishes on Thursday 22 July 2027: 1 Week.

How much does Pharmaceutical Stability Testing: ICH Study Design, Shelf-Life Statistics and OOT Control in Jeddah cost?

The fee for this date is 19,500 SAR per participant. Please read our cancellation policy before you book.

Is this date held in person or online?

It is held in person in Jeddah, at Corniche four-star.

Where else does Pharmaceutical Stability Testing: ICH Study Design, Shelf-Life Statistics and OOT Control run?

It is also scheduled in 7 other cities: Amsterdam, Barcelona, Dammam, Dubai, London, Paris and Riyadh.

What does this programme cover?

Pharmaceutical stability testing decides how long a medicine keeps its quality, yet many programmes run with protocols that miss storage conditions for target markets, analytical methods that cannot separate degradation products and shelf-life claims that rest on unpooled or over-extrapolated data. This Core Concept course trains QC, QA, regulatory affairs and R&D staff to design, run and evaluate stability studies against ICH Q1A(R2), Q1B, Q1D and Q1E and the WHO stability guidelines. Participants build a Stability Protocol and Shelf-Life Evaluation Pack for a product from their own portfolio.

The programme outline covers:

  • Introduction
  • Course Objectives
  • Target Audience
  • Course Outline
  • Day 1: Stability Programme Purpose, Degradation Science and Programme Review
  • Day 2: ICH Q1 Guidance Family, WHO Stability Guidelines and Study Types
  • Day 3: Stability Protocol Design, Sampling and Stability-Indicating Methods
  • Day 4: Shelf-Life Statistics, OOS and OOT Investigation and Chamber Control
  • Day 5: Stability Case Work, Dossier Presentation and Evaluation Pack
  • Skills You Will Gain
  • Why Attend This Course
  • Conclusion
Read the full outline on the programme page ↗

Where else does this programme run?

Also scheduled in 7 other cities.

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