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  1. Home/
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  3. Dr Mark Powell
Dr Mark Powell

Dr Mark Powell

Mark Powell Scientific Limited, UK, Director

Biography

Dr Mark Powell a Fellow of the Royal Society of Chemistry (RSC) with over thirty years’ experience as a senior analytical chemist. Mark has served as both Honorary Secretary and Honorary Treasurer of the RSC’s Analytical Division and led a working group on continuing professional development until July 2016. He has worked at a senior level in several companies with responsibility for analytical development and equipment qualification. In 2010 Mark was appointed Scientific Manager of a UK-based pharmaceutical CRO, with responsibility for guiding the direction of drug development programmes as well as establishing collaborations with academia and instrument manufacturers. In 2013, he set up his own company to provide training and consultancy services to the pharmaceutical industry. His consultancy work has involved, amongst other things, managing the analytical aspects of pharmaceutical development programmes and conducting data integrity audits. He is in demand as a trainer in topics such as pharmaceutical development, chromatography, spectroscopy, dissolution testing, data integrity, control of impurities, technical writing, and stability/stress studies.

Training Courses by Dr Mark Powell

Specifications for Small Molecule Drug Products
Pharma & Biotech

Specifications for Small Molecule Drug Products

Understand the importance of specifications in chemical drug products. Learn to develop and manage product specifications for regulatory compliance.

Date TBD
Online
Pharma & Biotech Stability Testing
Pharma & Biotech

Pharma & Biotech Stability Testing

Understand stability testing for pharmaceutical and biotech products. Learn guidelines, methods, and data interpretation.

Date TBD
Online
Dissolution Testing and Biowaivers
Pharma & Biotech
Analytical & Bioanalysis

Dissolution Testing and Biowaivers

This three-day online course covers both the theory and practical aspects of pharmaceutical dissolution testing for solid oral dosage forms.

Date TBD
Online
Analytical Method Development and Validation
Pharma & Biotech
Analytical & Bioanalysis

Analytical Method Development and Validation

Learn how to apply ICH Q14, Q2(R2), and USP to develop, validate, and manage analytical methods across their lifecycle.

Date TBD
Online
Extractables & Leachables Control Strategies
CMC
Pharma & Biotech

Extractables & Leachables Control Strategies

Gain practical skills in extractables and leachables risk assessment, study design, and regulatory compliance in this expert-led E&L training.

Date TBD
Online

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