Dissolution Testing: Apparatus Qualification, Method Development and f2 Profile Comparison – Paris, 26–30 Jul 2027
Dissolution Testing: Apparatus Qualification, Method Development and f2 Profile Comparison runs in Paris from Monday 26 July to Friday 30 July 2027 (1 Week). The fee is 23,500 SAR per participant. The same programme is also scheduled in 7 other cities.
- Dates
- Length
- 1 Week
- Fee per participant
- 23,500 SAR
- Format
- In person, Paris
- Venue
- Right Bank business hotel
- Status
- Open for registration
- Week
- 30 of 2027
- Reference
- 509_16846
This session
26–30 Jul 2027
This Dissolution Testing: Apparatus Qualification, Method Development and f2 Profile Comparison session in Paris runs from Monday 26 July to Friday 30 July 2027 (week 30, Q3 2027). It is the 1st 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?
- 26 – 30 July 2027 This date 23,500 SAR
- 1 – 5 November 2027 23,500 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_16846. 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 Paris start and finish?
It starts on Monday 26 July and finishes on Friday 30 July 2027: 1 Week.
How much does Dissolution Testing: Apparatus Qualification, Method Development and f2 Profile Comparison 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.
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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