Gaynor joined the MHRA as a GDP Inspector in May 2009 formally working in the pharmaceutical wholesale distribution industry for over 10 years as a Project Manager and Business Compliance Manager. Her roles included auditing the organisation to ensure legal compliance with regulatory bodies including compliance to GDP. Gaynor was also involved in a number of large projects including the management of a building project and the implementation of automation in a large distribution site. She has qualifications in Project Management and Health and Safety. Gaynor spent two years as the MHRA's Health and Safety Manager achieving BS18001 certification. She returned to her GDP Inspector role in July 2013 where she is a member of the implementation team for conducting inspections on API distributors and coordinator of the GDP symposium.

Peter is a pharmacist by profession and joined the MHRA in January 2013. Prior to joining the MHRA, Peter had worked in the pharmaceutical industry for over 30 years, focusing mainly on Pharmaceutical Wholesale and Retail Pharmacy.in various managerial roles including Operations Management, Regulatory Affairs, Quality Assurance and acted as Responsible Person for a number of companies in the UK. Peter has experience in the implementation of ISO 9001 and ISO 13485 Quality Systems and is an ISO Pharmaceutical Lead Auditor. He was an industry representative on the BAPW RP Committee, was instrumental in identifying some of the more recent examples of falsified medicines and is a member of the MHRA Falsified Medical Product Stakeholders Group.

Terry is an Inspector within the GDP Inspectorate at the Medicines and Healthcare products Regulatory Agency (MHRA). He joined the Agency in 2009 having previously worked over 25 years in a variety of pharmaceutical industry technical and managerial roles within R&D and QA.

Andrew joined the MHRA in January 2003 as a GLP inspector. In 2004 Andrew was appointed Operations Manager for the Good Laboratory Practise and Good Distribution Practise Groups, taking responsibility for the management of a team of ten inspectors. In May 2006 Andrew took on the role of Heads of the United Kingdom Good Laboratory Monitoring Authority. In this capacity he holds the chair of the OECD GLP Working Group and is a member of the EC GLP Working Group. Andrew has contributed to a number of national and international guidance documents including the first comprehensive European guidance for laboratories that perform the analysis of samples collected as part of clinical trials. In 2014 Andrew was appointed to the role of Unit Manager Inspectorate Operations with responsibility for the GLP, GCP and GDP inspection teams. Prior to joining the MHRA, Andrew worked in academia for a number of years performing research on the underlying causes of cardiovascular disease before moving into the pharmaceutical sector where he was involved in pre-clinical drug development.

Bernadette is a GDP Inspector and joined the MHRA in March 2005. Her previous experience includes local government enforcement duties within a Trading Standards environment. Bernadette spent 10 years working as an Investigator within the MHRA Enforcement and Intelligence division dealing with criminal investigations. She has played an important role in the year on year success of the MHRA's Operation Pangea which focuses on the illegal internet trade of medicines and medical devices globally. In 2015, £15.8 million worth of fake medicines and devices were seized during UK operations. Bernadette is an accredited Counter Fraud Specialist.

Naseem has been with the MHRA since 2006 and is an Intelligence Analyst in the Enforcement Groups Intelligence Unit. In 2006 Naseem completed the Covert Internet Investigators course run by the National Centre for Policing Excellence. He is currently the Enforcement Group’s Covert Internet Investigator and responsible for the conduct of internet investigations and covert internet test purchases. Naseem has also completed the Initial Analytical Techniques Course run by the National Policing Improvement Agency. Before Joining the MHRA in 2005, he completed an LLB (Hons) and MA in Intelligence & International Security.

Bio Available Soon

Sandra joined the MHRA as Manager of the DMRC in 2015. She is a Chartered Chemist and a Qualified Person, and has over thirty years experience in the pharmaceutical industry. She has worked in large multi-nationals, as well as medium and small start up companies. As a QP, Sandra has expertise in GMP and pharmaceutical quality systems. Through her earlier roles in R&D Analytical Development she gained knowledge of stability testing of formulated products and active substances, and in New Product Introduction was involved in cleaning validation and technology transfer.

Peter joined the MHRA in 1993, having spent the previous three years with the Department of Health and NHS Management Executive in Leeds. Peter initially worked in the Enforcement Group and was responsible for conducting a two-year project into the use of Traditional Chinese Medicines in the UK before managing the unit's criminal prosecution team. Peter joined the GDP Inspectorate in June 2002 and became an Operations Manager in November 2011 and a Senior Inspector in 2016. Peter currently leads one of the GDP Inspectorates two operational teams and combines this role with being a member of the GDP Inspectorates Senior Inspector Group.  

Claire joined the agency as a GDP Inspector in January 2013 and has a background in pharmaceutical manufacturing and auditing of 15 years. Aspects of previous roles in a large pharmaceutical company include project management, QMS implementation and Quality Assurance. She is PRINCE2 qualified and has a degree in Business.

Madeleine is a senior GDP inspector and joined the MHRA in August 2009. Her previous experience includes NHS pharmacy manufacturing, project management in NHS Blood and Transplant and some teaching within the NHS. Recent projects include working with Cogent to develop the RP Gold Standard and working with the Maritime and Coastguard Agency to improve compliance within the marine sector. Madeleine enjoys contributing to inspector development and inspection consistency. Madeleine is registered with the General Pharmaceutical Council.

Phil joined the MHRA in the Pharmacovigilance Inspectorate in July 2009. In 2010 he moved to the GDP Inspectorate, where he became a GDP Operations Manager in 2013. He is a pharmacist by profession, who initially worked in the pharmaceutical industry for over 30 years, for 4 different global pharmaceutical companies. His positions included different managerial and project leader roles at all stages of pharmaceutical development. Phil currently manages one of the GDP Inspectorates two operational teams.

Tony was a founder member of the GDP Inspectorate when it was created in 2001 and is a Senior GDP Inspector responsible for inspecting the full range of UK distribution companies. He is a member of the PIC/S GDP working group, working on the training and aligning of GDP standards for PIC/S member countries. He was part of the EMA GDP drafting group preparing the GDP Guidelines and updates to the compilation of community procedures and involved in training the GMDP inspectors on the new guidelines. He was also a member of the team who reviewed the UK supply chain and looked at ways to improve the standard of the Wholesale Dealer 'Responsible Person'. He is currently a member of the implementation team for the Falsified Medicines Directive and working on developing the new Risk Based Inspection IT system for the MHRA. Tony has been with the MHRA for 24 years, working initially with the MHRA Enforcement Group where he was a Senior Investigation Officer. As such he was responsible for investigating counterfeit medicines, internet sales and other illegal activity with pharmaceuticals.

Cheryl joined the MHRA as a GDP inspector in 2005. Cheryl is a Chartered Chemist and spent many years working within industry as a research chemist during which time she filed a number of patents both European and Worldwide. She has extensive experience working within Project and Programme Management roles with responsibility for a wide range of projects spanning various scientific and engineering disciplines. As well a performing a full range of GDP inspections nationwide, Cheryl was the MHRA representative on the GDP drafting Group at the EMA. Since the current guidance has been implemented, Cheryl has been leading the project to raise awareness within the medicines supply chain that companies and sites not previously regulated are impacted by the change in legislation.

Jacqui joined the GDP Inspectorate in April 2011 and is responsible for inspecting the full range of UK distribution companies nationwide.  Jacqui holds a degree in Pharmacology and prior to joining the MHRA GDP Inspectorate, Jacqui worked in the MHRA Licensing Division as a Scientific Assessor.  Jacqui acted briefly as GDP Operations Manager in 2017. Jacqui enjoys contributing to inspector development and stakeholder engagement; currently involved in NHS Project work.

Gaynor joined the MHRA as a GDP Inspector in May 2009 formally working in the pharmaceutical wholesale distribution industry for over 10 years as a Project Manager and Business Compliance Manager. Her roles included auditing the organisation to ensure legal compliance with regulatory bodies including compliance to GDP. Gaynor was also involved in a number of large projects including the management of a building project and the implementation of automation in a large distribution site. She has qualifications in Project Management and Health and Safety. Gaynor spent two years as the MHRA's Health and Safety Manager achieving BS18001 certification. She returned to her GDP Inspector role in July 2013 where she is a member of the implementation team for conducting inspections on API distributors and coordinator of the GDP symposium.

Peter is a pharmacist by profession and joined the MHRA in January 2013. Prior to joining the MHRA, Peter had worked in the pharmaceutical industry for over 30 years, focusing mainly on Pharmaceutical Wholesale and Retail Pharmacy.in various managerial roles including Operations Management, Regulatory Affairs, Quality Assurance and acted as Responsible Person for a number of companies in the UK. Peter has experience in the implementation of ISO 9001 and ISO 13485 Quality Systems and is an ISO Pharmaceutical Lead Auditor. He was an industry representative on the BAPW RP Committee, was instrumental in identifying some of the more recent examples of falsified medicines and is a member of the MHRA Falsified Medical Product Stakeholders Group.

Terry is an Inspector within the GDP Inspectorate at the Medicines and Healthcare products Regulatory Agency (MHRA). He joined the Agency in 2009 having previously worked over 25 years in a variety of pharmaceutical industry technical and managerial roles within R&D and QA.

Andrew joined the MHRA in January 2003 as a GLP inspector. In 2004 Andrew was appointed Operations Manager for the Good Laboratory Practise and Good Distribution Practise Groups, taking responsibility for the management of a team of ten inspectors. In May 2006 Andrew took on the role of Heads of the United Kingdom Good Laboratory Monitoring Authority. In this capacity he holds the chair of the OECD GLP Working Group and is a member of the EC GLP Working Group. Andrew has contributed to a number of national and international guidance documents including the first comprehensive European guidance for laboratories that perform the analysis of samples collected as part of clinical trials. In 2014 Andrew was appointed to the role of Unit Manager Inspectorate Operations with responsibility for the GLP, GCP and GDP inspection teams. Prior to joining the MHRA, Andrew worked in academia for a number of years performing research on the underlying causes of cardiovascular disease before moving into the pharmaceutical sector where he was involved in pre-clinical drug development.

Bernadette is a GDP Inspector and joined the MHRA in March 2005. Her previous experience includes local government enforcement duties within a Trading Standards environment. Bernadette spent 10 years working as an Investigator within the MHRA Enforcement and Intelligence division dealing with criminal investigations. She has played an important role in the year on year success of the MHRA's Operation Pangea which focuses on the illegal internet trade of medicines and medical devices globally. In 2015, £15.8 million worth of fake medicines and devices were seized during UK operations. Bernadette is an accredited Counter Fraud Specialist.

Naseem has been with the MHRA since 2006 and is an Intelligence Analyst in the Enforcement Groups Intelligence Unit. In 2006 Naseem completed the Covert Internet Investigators course run by the National Centre for Policing Excellence. He is currently the Enforcement Group’s Covert Internet Investigator and responsible for the conduct of internet investigations and covert internet test purchases. Naseem has also completed the Initial Analytical Techniques Course run by the National Policing Improvement Agency. Before Joining the MHRA in 2005, he completed an LLB (Hons) and MA in Intelligence & International Security.

Bio Available Soon

Sandra joined the MHRA as Manager of the DMRC in 2015. She is a Chartered Chemist and a Qualified Person, and has over thirty years experience in the pharmaceutical industry. She has worked in large multi-nationals, as well as medium and small start up companies. As a QP, Sandra has expertise in GMP and pharmaceutical quality systems. Through her earlier roles in R&D Analytical Development she gained knowledge of stability testing of formulated products and active substances, and in New Product Introduction was involved in cleaning validation and technology transfer.

Peter joined the MHRA in 1993, having spent the previous three years with the Department of Health and NHS Management Executive in Leeds. Peter initially worked in the Enforcement Group and was responsible for conducting a two-year project into the use of Traditional Chinese Medicines in the UK before managing the unit's criminal prosecution team. Peter joined the GDP Inspectorate in June 2002 and became an Operations Manager in November 2011 and a Senior Inspector in 2016. Peter currently leads one of the GDP Inspectorates two operational teams and combines this role with being a member of the GDP Inspectorates Senior Inspector Group.  

Claire joined the agency as a GDP Inspector in January 2013 and has a background in pharmaceutical manufacturing and auditing of 15 years. Aspects of previous roles in a large pharmaceutical company include project management, QMS implementation and Quality Assurance. She is PRINCE2 qualified and has a degree in Business.

Madeleine is a senior GDP inspector and joined the MHRA in August 2009. Her previous experience includes NHS pharmacy manufacturing, project management in NHS Blood and Transplant and some teaching within the NHS. Recent projects include working with Cogent to develop the RP Gold Standard and working with the Maritime and Coastguard Agency to improve compliance within the marine sector. Madeleine enjoys contributing to inspector development and inspection consistency. Madeleine is registered with the General Pharmaceutical Council.

Phil joined the MHRA in the Pharmacovigilance Inspectorate in July 2009. In 2010 he moved to the GDP Inspectorate, where he became a GDP Operations Manager in 2013. He is a pharmacist by profession, who initially worked in the pharmaceutical industry for over 30 years, for 4 different global pharmaceutical companies. His positions included different managerial and project leader roles at all stages of pharmaceutical development. Phil currently manages one of the GDP Inspectorates two operational teams.

Tony was a founder member of the GDP Inspectorate when it was created in 2001 and is a Senior GDP Inspector responsible for inspecting the full range of UK distribution companies. He is a member of the PIC/S GDP working group, working on the training and aligning of GDP standards for PIC/S member countries. He was part of the EMA GDP drafting group preparing the GDP Guidelines and updates to the compilation of community procedures and involved in training the GMDP inspectors on the new guidelines. He was also a member of the team who reviewed the UK supply chain and looked at ways to improve the standard of the Wholesale Dealer 'Responsible Person'. He is currently a member of the implementation team for the Falsified Medicines Directive and working on developing the new Risk Based Inspection IT system for the MHRA. Tony has been with the MHRA for 24 years, working initially with the MHRA Enforcement Group where he was a Senior Investigation Officer. As such he was responsible for investigating counterfeit medicines, internet sales and other illegal activity with pharmaceuticals.

Cheryl joined the MHRA as a GDP inspector in 2005. Cheryl is a Chartered Chemist and spent many years working within industry as a research chemist during which time she filed a number of patents both European and Worldwide. She has extensive experience working within Project and Programme Management roles with responsibility for a wide range of projects spanning various scientific and engineering disciplines. As well a performing a full range of GDP inspections nationwide, Cheryl was the MHRA representative on the GDP drafting Group at the EMA. Since the current guidance has been implemented, Cheryl has been leading the project to raise awareness within the medicines supply chain that companies and sites not previously regulated are impacted by the change in legislation.

Jacqui joined the GDP Inspectorate in April 2011 and is responsible for inspecting the full range of UK distribution companies nationwide.  Jacqui holds a degree in Pharmacology and prior to joining the MHRA GDP Inspectorate, Jacqui worked in the MHRA Licensing Division as a Scientific Assessor.  Jacqui acted briefly as GDP Operations Manager in 2017. Jacqui enjoys contributing to inspector development and stakeholder engagement; currently involved in NHS Project work.