Dissolution Testing: Apparatus Qualification, Method Development and f2 Profile Comparison – Barcelona, 15–19 Nov 2027
Dissolution Testing: Apparatus Qualification, Method Development and f2 Profile Comparison runs in Barcelona from Monday 15 November to Friday 19 November 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, Barcelona
- Venue
- Eixample district four-star
- Status
- Open for registration
- Week
- 46 of 2027
- Reference
- 509_16847
This session
15–19 Nov 2027
This Dissolution Testing: Apparatus Qualification, Method Development and f2 Profile Comparison session in Barcelona runs from Monday 15 November to Friday 19 November 2027 (week 46, Q4 2027). It is the only date in Barcelona in 2027, at a fee of 23,500 SAR. Registration is open for this date. It is held in person at Eixample district 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: 509_16847. Quote it when you contact us.
Before you book, read our cancellation policy.
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Questions about this date
When does Dissolution Testing: Apparatus Qualification, Method Development and f2 Profile Comparison in Barcelona start and finish?
It starts on Monday 15 November and finishes on Friday 19 November 2027: 1 Week.
How much does Dissolution Testing: Apparatus Qualification, Method Development and f2 Profile Comparison in Barcelona 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 Barcelona, at Eixample district 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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