About us
The BGMA represents the interests of UK based manufacturers and suppliers of generic medicines and promotes the development of the generic medicines industry in the United Kingdom.
The British Generic Manufacturers Association (BGMA) is made up of members of the generic manufacturing supply industry, who between them account for approximately 85% of the total UK generic market by volume.
A key feature of the strong generics industry in the UK is that it introduces competition to the supply of prescription medicines making them more affordable to the NHS and enhancing their availability to patients.
According to NHS figures (NHS Digital), more than a billion items are prescribed generically every year. The increase of generic prescriptions, allied with a reduction in the net ingredients costs, means that overall savings to the NHS medicines bill have now passed more than £13 billion annually.
Our industry’s mission is centred around increasing patient access to life saving and life changing medicines. We do this by bringing competition to the medicines marketplace at the molecule level when patents (and / or any data or market exclusivity) expire.
This competition reduces market prices, enhances security of supply, and fosters incremental and primary innovation—all of which support increasing patient access. Examples of innovation include new administrations and dosage strengths.
The evidence is that this sort of competition controls the price of medicines more effectively than direct intervention. We believe, therefore, that direct price control by the Government should only be employed where competition has been shown to be ineffective.
Looking at 40 originator products to come off patent since the start of 2014, the introduction of generics saw sales prices reduce by an average of 89% in this time.
85%
Total UK market by volume
1bn
Items prescribed generically every year.
Quality forum
The British Generic Manufacturers Association (BGMA) in conjunction with the regulatory body the MHRA, runs a successful forum focusing on ensuring the manufacturing quality of generic medicines in the UK.
The group meets three times a year to share and discuss the latest issues which impact on the quality of generic medicines. The forum brings together generic medicines companies, those who provide manufacturing and quality control services, as well as the MHRA.
Paul Fleming, the BGMA’s Technical Director, said: “As regulatory requirements and supply chains become ever more complex, supporting high quality standards is vitally important for the pharmaceutical industry, patients and the value we deliver to the NHS. From a generic medicines perspective, the forum is an important outlet which is closely aligned with the regulator allowing increased mutual understanding as well as the ability to share the latest information quickly and easily.
“Quality is a key component in ensuring that patients get their medicines in a timely and affordable manner. Our forum provides a vital conduit between industry and the regulator on a topic which is critically important to the successful operation of the generic medicines marketplace in the UK, Europe and internationally.”
The Quality Forum is open to full and associate members of the BGMA. To find out about joining contact Jeremy Durrant
jeremy.durrant@
britishgenerics.co.uk
02078667883
BGMA structure
The BGMA operates through a series of expert working groups that cover Regulatory Affairs, Economic & Commercial (Pricing, Reimbursement, Market Access, etc), Secondary Care, Sustainability, NHS Partnership, Legal Issues and a specialist sector group on Biosimilars via our sister organisation the British Biosimilars Association (BBA www.britishbiosimilars.co.uk). These groups are overseen by the Board.
The working group chairs and vice-chairs are elected by the members of each group and ratified by the Board, which is the Association's decision making body and which meets six times a year.
The working group chairs and vice-chairs report and recommend to the Board, thus ensuring that the Association's policies and activities are member-driven and that all members have an equal input to the decision making.
BGMA executive team
The day-to-day running of the BGMA is headed by Mark Samuels, the association's chief executive and a secretariat. The BGMA also elects a chairperson and vice-chairperson on a rotational basis drawn from the membership. The current chair is Diane DiGangi Trench.
Diane DiGangi Trench
Chair
Diane is the Chair of the British Generic Manufacturers Association. The Country Head of Sandoz UK has more than 25 years of pharmaceutical industry experience and has held a number of senior commercial roles including stints with Takeda and Astra Zeneca. She joined Sandoz in 2018 in the US, where she served as Vice-President, Market Access and Patient Services. In 2021, she became the head of Sandoz’ UK business and in her two years in role, she has led the organisation through a post-COVID recovery and growth phase to prepare for the proposed spin out of the company from its parent, Novartis.
Paul BurdenPaul Burden
Vice Chair
Paul is the vice-chair of the British Generic Manufacturers Association (BGMA) and the UK Vice President Rx for Stada Thornton & Ross. He has 25 years’ experience in the off-patent sector and prior to his current position, held a variety of commercial roles with companies such as Arrow Generics, Mylan, Teva and Advanz. At an association level he has been involved with the BGMA since 2011 including chairing the economic and commercial working group for four years. He has helped shape the BGMA’s priorities and position on topics such as generic pricing, falsified medicines directive, economic data, voluntary schemes, and supply chain issues.
Diane DiGangi TrenchMark SamuelsMark Samuels
CEO
Mark is the Chief Executive of both British Generic Manufacturers Association (BGMA) as well as its sister body the British Biosimilars Association (BBA). Mark’s career has spanned diverse experience across the life sciences sector. He is a former executive at Roche and co-founded the Medicines Discovery Catapult Ltd. He was the founding Managing Director of the government’s Office for Clinical Research Infrastructure – instrumental in managing the Department of Health’s £0.6 billion/year investment in research centres across the NHS. Mark served for seven years on the Chief Medical Officer for England’s strategy board for health research, and he has worked with Number 10 to contribute to the Prime Minister’s strategy for life sciences.
Paul BurdenRobert Russel-PavierRobert Russell-Pavier
Economics Director
Robert has worked for the BGMA since 2009. In his current role, Rob initiates and supports the BGMA’s engagement with Government, Parliamentarians, as well as relevant health bodies and other stakeholders, regarding the public reimbursement, pricing and procurement of medicines in both primary and secondary care. Among other areas, Rob is currently focused on helping the Association to articulate its position around the developing homecare market.
Mark SamuelsJeremy DurrantJeremy Durrant
Communications Director
Jeremy has worked with the BGMA since 2011 and heads up all internal and external communications activity on behalf of the association. He also is actively involved in stakeholder engagement, membership services, events and networking.
Robert Russell-PavierPaul FlemingPaul Fleming
Technical Director, British Generic Manufacturers Association
Paul Fleming is Technical Director of the British Generic Manufacturers Association (BGMA) and the British Biosimilars Association (BBA). The roles include close and regular working with MHRA, Department of Health and Social Care, the NHS, UK Government and other stakeholders. At a European level, Paul is a member of the regulatory and quality committees of Medicines for Europe. In 2015 he wrote the Regulatory Efficiency Report for EGA, setting out a wide range of recommendations identifying opportunities for improvement within the regulatory system for generic medicines.. Paul has 15 years’ experience from working in the generic sector of the European pharmaceutical industry, in a variety of senior board level roles covering R&D, drug regulation, pharmacovigilance and clinical development. Earlier in his career Paul spent six years with the MHRA as a pharmaceutical assessor. He is a registered pharmacist and holds a higher degree in pharmaceutical technology. Throughout his professional life Paul has maintained an involvement with the science of pharmaceutical development connecting to how medicines can be used for the maximum benefit of patients and the NHS.
Jeremy DurrantOur members
Disclosure
Disclosure of transfers of value in 2023
As an affiliate of Medicines for Europe, and based on its Code of Conduct, BGMA asks that member companies record and publish their transfers of value (in kind or actual) for the previous calendar year (2023) to healthcare professionals, healthcare organisations and patient organisations. Members can publish their return by any one of the following three ways:
- On companies' websites
- On other publicly accessible websites (notably on Disclosure UK)
- On the BGMA's website
The following companies have requested for the BGMA to publish their annual transfers of value for 2023.
| Company | Name of healthcare organisation, patient organisation or number of healthcare professionals that received a transfer of value | Category of transfer of value (fee for service / consultancy, conference, meeting or event sponsorship, grants and donations, other) | Total value |
|---|---|---|---|
| Aspire Pharma | NHS Confederation Services Company Ltd | Two conferences | £9,150 |
| Primary Care Respiratory Society UK | Conference | £4,233 | |
| Primary Care Commissioning CIC | Conference | £1,997 | |
| National Paediatric Respiratory & Allergy Nurses Group Meeting | Meeting sponsorship | £625 | |
| Antibiotic Research UK | Charity donation towards the delivery of the charity's annual event | £6,000 | |
| 21 healthcare professionals | All for consultancy support, ranging from £200 to £44,816.25, with an average fee of £3,306.81 | £69,443 | |
| Hikma (UK) | Nil return | ||
| Niche Generics Limited | Nil return | ||
| Panpharma UK Ltd | Nil return | ||
| Reig Jofre UK | Nil return | ||
| Rivopharm UK Ltd | Nil return |
For queries, please contact robert.russellpavier@britishgenerics.co.uk
Our core focus
Patients
Making medicines more affordable to the NHS and therefore increasing patient access to important, and potentially life-saving, drugs is a key role of the UK generic and biosimilar medicines industry. The NHS faces major funding challenges due to increased demand from an ageing population as well as the rising cost of new technologies and drugs. Generic competition already saves the NHS more than £13bn a year and allows further investment in new drugs which can support unmet patient need.
Case studies
Generic equivalent
Manufacture of Atorvastatin - the generic equivalent of the top-selling global branded drug Lipitor - has saved the National Health Service (NHS) more than £350million in the first 12 months following the expiration of Pfizer’s patent exclusivity.
Consistent information
To improve consistent information to patients and significantly reduce the prohibitive cost to the industry and the regulator of each company user-testing every single patient information leaflet (PIL) - at a cost per test in the region of £10,000 - the BGMA co-ordinated user testing of a limited number of typical PILs ensuring that patients received the benefit of common wording for each product irrespective of the manufacturer.
Quality
Generic medicines in the UK must comply with exactly the same standards of quality, safety and efficacy as all medicinal products. They are produced in regularly inspected plants by the UK medicines regulator the MHRA. Just like originator products, once a generic medicine is sold on the market, it must be monitored by the manufacturer in case any adverse reactions are reported.
Case studies
Quality forum
The BGMA runs a forum in conjunction with the MHRA to focus on issues and guidance relating to quality. The group meets three times a year to share and discuss the latest information which impacts quality in the generics industry from auditing and inspections through to data integrity and issues surrounding API.
Value
The UK generics industry is the engine room behind a virtuous circle of innovation and cost containment. Each year more than 1billion items are prescribed generically in England and Wales unlocking significant savings for the NHS. As well as delivering cost-savings, generics also provide value through a number of means not least widening accessibility.
Case studies
Innovation
One of our members developed a liquid version of a product which was previously only available in solid dose. This enabled children and adults with swallowing difficulties (such as following a stroke where there is paralysis of the mouth) to access the drug safely.
New therapeutic entities
Other BGMA members are looking at new therapeutic entities, which are based on the molecule, and formulated, delivered or used in a novel way to meet unmet patient need. These include a new route of delivering a Parkinson’s disease drug, a beta blocker as a once a day glaucoma remedy, and an extended-release once a month and once every three months injection of risperidone (to treat schizophrenia).
Sustainability
The generic industry in the UK is amongst the most efficient in the world with prices currently amongst the lowest in Europe. Competitive prices, and proportionate regulation are required, if the industry is to continue to deliver savings as well as fund the necessary development of the more complex medicines, including biosimilars.
Case studies
Challenges to the industry
The British Generic Manufacturers Association (BGMA) and the Department of Health signed an agreement to work to explore potential challenges to the sustainability of the generic pharmaceutical industry in England. Based on proposals from the BGMA, the Department will facilitate conversations across government to understand issues and to identify where appropriate action can be taken.
Partnership
The UK generics industry is a key part of an efficient supply chain which ensures patients access the medicines they need in a timely and affordable manner. As part of this manufacturers liaise regularly with Government, regulators and commissioners to ensure product safety, quality and certainty of supply.
Case studies
New product registrations
In the key area of new product registrations, BGMA has been closely surveying MHRA performance year on year and identifying areas requiring improvement, for discussion with the regulator. This has resulted in major improvement in the time taken for new generic medicines to be registered in the UK. This is greatly assisting the predictable timely availability of generic medicines for patients, healthcare professionals and has also resulted in NHS cost savings.
With the increasing weight of new legislation coming from Europe, the BGMA continues to work closely with MHRA to ensure its drafting and UK implementation is well managed, and minimises red tape and over regulation.
Cross-industry group membership
The BGMA is a member of the cross-industry group the NHS Pharmaceutical Sector Board alongside NHS England and the Association of the British Pharmaceutical Industry (ABPI).
Breakthrough project with the MHRA
The BGMA successfully completed a breakthrough project with the MHRA involving 12 separate generic companies which were required to communicate information for the diabetic drug Pioglitazone.
The project saw safety information centrally co-ordinated by the BGMA on behalf of the 12 companies which was then approved by the MHRA and sent to healthcare professionals. This meant the regulator was not required to approve 12 separate applications and those receiving the mailings received one set of consistent, clear information.