Practical Management of Impurities and Development of Effective and Comprehensive Control Strategies

Date: 21 March - 29 March 2023

Location: Online Platform

Tutors: Dr Andrew Teasdale

This Online course is aimed at providing a holistic understanding of the challenges and issues associated with implementing an effective control strategy for all impurity types. It will examine key areas, specifically, impurity qualification, mutagenic impurities, elemental impurities, extractives and leachables and solvents. In each case, it will examine practical approaches through both case studies and practical exercises and in all instances provide clarity as to the current and emerging regulatory frameworks.

The course also looks at other impurity related areas such as shared facilities, both the guideline and recent Q&A document, finishing with a look to the future and the challenges associated with new modalities including Oligonucleotides and Antibody Drug Conjugates.

The course will be split over four sessions as follows in UK time:

Tuesday, March 21 | 1.30pm – 5.30pm GMT
Wednesday, March 22 | 1.30pm – 5.30pm GMT

Tuesday, March 28 | 1.30pm – 5.30pm GMT
Wednesday, March 29 | 1.30pm – 5.30pm GMT

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Course Outline

This 4 session online course is aimed at providing a holistic understanding of the challenges and issues associated with implementing an effective control strategy for all impurity types. It will examine key areas, specifically, impurity qualification, mutagenic impurities, elemental impurities, extractives and leachables and solvents. In each case it will examine practical approaches through both case studies and practical exercises and in all instances provide clarity as to the current and emerging regulatory frameworks

Benefits of Attending

What will attendees gain from the course?
  • What are the key impurity classes and how they relate to the overall manufacturing process.
  • A clear understanding of the pivotal role played by chemists and analysts in the impurity management process.
  • How to effectively relate product quality to impurity qualification ensuring that qualification studies properly align to process capability.
  • How to align impurity management to the over process control strategy – to optimise effective control.
  • How to use effective impurity management to drive key process and regulatory decisions e.g. starting material definition and defence.

Who Should Attend

Scientists, managers and team leaders involved in the development of pharmaceuticals and Engineers.  This course is particularly relevant to process development chemists and analysts at all levels, but will also be of interest to late stage medicinal chemists who want to gain a greater understanding of the impact of impurities

What's Included

The course fee includes:

  • Link to watch all four live sessions
  • Electronic version of the course manual*
  • Course certificate

For this on line course, there will be no recordings available and *the e reader manual is NOT printable or downloadable (due to copyright).  If you prefer a hard copy of the manual you will have the opportunity of purchasing a professionally printed hard copy during the booking process.

Testimonials

Impurities Course - Online Delegate 2021

Very relevant material by a dedicated lecturer. Surprisingly interactive despite being online.

Impurities Course - Online Delegate 2021

Excellent course in terms of organization as well as presentation of educational materials. Highly recommended.

Impurities Course - Online Delegate 2021

The course is highly recommended for everyone writing assessments in pharma industry

Impurities Online Delegate - 2021

The course was incredibly helpful in understanding current key topics in impurity management. A valuable course for anyone involved in DS or DP manufacture!

Impurities Online Delegate - 2021

Up to date course and very worth while for new as well as experienced persons in the field!

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Practical Management of Impurities and Development of Effective and Comprehensive Control Strategies

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Practical Management of Impurities and Development of Effective and Comprehensive Control Strategies

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