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Mr Bonner Richard

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Mr Bonner Richard
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  • His expertise includes all API manufacture as well as biotech and fermentation operations, solid dosage forms and all service areas such as quality control laboratories, quality system implementation, stability functions, process validations and management systems. In addition Mr Bonner frequently lectures and runs workshops on all aspects of QA, GMPs and on auditing skills both in Europe and the USA.

Richard Bonner is a Biochemistry graduate and is currently located in the UK and works as a consultant to the pharmaceutical industry. He is now the Director of Regulatory Affairs for the European Compliance Academy (ECA) interfacing with international regulatory agencies around the world. Mr Bonner is a member of the ECA Advisory Board and also a Member of the Advisory Board of the European QP Association. His expertise includes all API manufacture as well as biotech and fermentation operations, solid dosage forms and all service areas such as quality control laboratories, quality system implementation, stability functions, process validations and management systems. In addition Mr Bonner frequently lectures and runs workshops on all aspects of QA, GMPs and on auditing skills both in Europe and the USA.

Previous to his current role he was a senior quality adviser for Eli Lilly and Company having spent several years as a Director of regulatory affairs, quality control and quality assurance functions. He has 31 years experience within the pharmaceutical industry working in production, technical-services and human resources as well as quality control and quality assurance functions.

He has been involved in multiple inspections on the part of MHRA, FDA, EMEA and other authorities. He has also been instrumental in obtaining ISO 9000-2000 accreditation for manufacturing sites. In addition, he has audited extensively throughout the EU and in countries such as Canada, USA, China, Pakistan, India, Egypt, Syria, Oman and Russia. He is also a Qualified Person in Europe.

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