Dissolution Testing: Apparatus Qualification, Method Development and f2 Profile Comparison – London, 7–11 Dec 2026
Dissolution Testing: Apparatus Qualification, Method Development and f2 Profile Comparison runs in London from Monday 7 December to Friday 11 December 2026 (1 Week). The fee is 23,000 SAR per participant. The same programme is also scheduled in 7 other cities.
- Dates
- Length
- 1 Week
- Fee per participant
- 23,000 SAR
- Format
- In person, London
- Venue
- Central London four-star
- Status
- Open for registration
- Week
- 50 of 2026
- Reference
- 509_16844
This session
7–11 Dec 2026
This Dissolution Testing: Apparatus Qualification, Method Development and f2 Profile Comparison session in London runs from Monday 7 December to Friday 11 December 2026 (week 50, Q4 2026). It is the only date in London in 2026, at a fee of 23,000 SAR, the same for each of them. Registration is open for this date. It is held in person at Central London four-star.
When else does it run in London?
- 7 – 11 December 2026 This date 23,000 SAR
- 13 – 17 September 2027 23,000 SAR
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: 509_16844. 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 Dissolution Testing: Apparatus Qualification, Method Development and f2 Profile Comparison in London start and finish?
It starts on Monday 7 December and finishes on Friday 11 December 2026: 1 Week.
How much does Dissolution Testing: Apparatus Qualification, Method Development and f2 Profile Comparison in London cost?
The fee for this date is 23,000 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 London, at Central London four-star.
What does this programme cover?
Dissolution testing links a solid oral dosage form's release behaviour to batch quality and, through biopharmaceutics, to how the medicine performs in patients. Yet many laboratories run methods with poorly justified media, apparatus that drift out of mechanical calibration and profile comparisons that fail scientific review. This Core Concept course trains QC analysts, formulation scientists and analytical development staff to qualify dissolution apparatus, control sources of variability, develop and validate discriminating methods, apply stage testing and compare profiles with the f2 similarity factor. Participants build a Dissolution Method Development and Justification Report for a case tablet.
The programme outline covers:
- Introduction
- Course Objectives
- Target Audience
- Course Outline
- Day 1: Dissolution Purpose, Biopharmaceutics and Laboratory Baseline
- Day 2: Pharmacopoeial Apparatus, Qualification and Variability Control
- Day 3: Dissolution Method Development and Analytical Finish
- Day 4: Validation, Acceptance Criteria, Profile Comparison and Investigations
- Day 5: Case Tablet Method Development and Justification Report
- Skills You Will Gain
- Why Attend This Course
- Conclusion
Where else does this programme run?
Also scheduled in 7 other cities.
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