Quality & Productivity

Pharmaceutical Stability Testing: ICH Study Design, Shelf-Life Statistics and OOT Control – Paris, 8–12 Nov 2027

Pharmaceutical Stability Testing: ICH Study Design, Shelf-Life Statistics and OOT Control runs in Paris from Monday 8 November to Friday 12 November 2027 (1 Week). The fee is 23,500 SAR per participant. The same programme is also scheduled in 7 other cities.

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Dates
Length
1 Week
Fee per participant
23,500 SAR
Format
In person, Paris
Venue
Right Bank business hotel
Status
Open for registration
Week
45 of 2027
Reference
382_13414

This session

8–12 Nov 2027

This Pharmaceutical Stability Testing: ICH Study Design, Shelf-Life Statistics and OOT Control session in Paris runs from Monday 8 November to Friday 12 November 2027 (week 45, Q4 2027). It is the 2nd of 2 dates in Paris in 2027, at a fee of 23,500 SAR, the same for each of them. Registration is open for this date. It is held in person at Right Bank business hotel.

When else does it run in Paris?

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_13414. Quote it when you contact us.

Before you book, read our cancellation policy.

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Questions about this date

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

It starts on Monday 8 November and finishes on Friday 12 November 2027: 1 Week.

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

The fee for this date is 23,500 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 Paris, at Right Bank business hotel.

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, Jeddah, London 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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