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Mark Powell

Director, Mark Powell Scientific Limited

Mark Powell set up Mark Powell Scientific Limited to provide technical support for pre-clinical drug development, which may involve short-term help with specific problems or management of the analytical aspects of a development project, for new or existing compounds, as part of a multi-disciplinary team. He has an expertise in analytical method development and validation (including assay of impurities), design of stability testing studies and auditing of contract laboratories. Mark is also an experienced quality auditor, and can perform GMP audits of contract laboratories, including evaluation of compliance with data integrity requirements.

He also provides training services, which are accredited by the UK's vocational skills agency, Cogent SSC, and are designed to ensure that analysts have the necessary theoretical and practical skills to perform their jobs competently. As well as courses in instrumental chemical analysis, He also provides training in basic laboratory skills and technical writing (analytical methods, SOPs and technical reports). Mark has recently been working with Spectroscopy Magazine to write and deliver an on-line training course in UV spectroscopy and has also been asked to provide training on behalf of the chromatography consumable company Hichrom.



  •  Friday, January 25, 2019
  • 11:00 AM EST,
  • 60 Minutes
  • ¤115.00
Analytical Instrument Qualification According to USP General Chapter - 1058

The webinar will cover the essential elements of analytical instrument qualification (hardware and software) and will enable attendees to adopt a compliant approach.





  • Recorded
  • View Anytime
  • 60 Minutes
  • ¤155.00
Analytical Instrument Qualification According to USP General Chapter - 1058

The webinar will cover the essential elements of analytical instrument qualification (hardware and software) and will enable attendees to adopt a compliant approach.

300001sem
Mark Powell
Date: 13 & 14 August, 2018   |   Time: 09:00 AM To 05:00 PM CEST

Pharmaceutical Data Integrity

The current regulatory focus on data integrity means that all personnel engaged in pharmaceutical manufacturing and testing need to be aware of regulators’ expectations. Data integrity breaches can occur accidentally

Price: ¤999.00

300002sem
Mark Powell
Date: 26 & 27 November, 2019   |   Time: 09:00 AM To 05:00 PM CEST

Pharmaceutical GMP Regulations

Compliance with pharmaceutical GMP regulations is essential for companies manufacturing or testing drugs or drug products for human/veterinary use.

Price: ¤999.00