Chair
Prof Jones was Head of R&D at Wellcome plc, where he orchestrated the development of several groundbreaking pharmaceutical products. His leadership extended to various pivotal roles, including serving as a main board director for Research & Development at Wellcome and contributing to the boards of companies like Allergan and VeronaPharma.
Beyond his corporate achievements, his academic endeavors have been equally noteworthy. As a visiting professor at King’s College London, he has nurtured budding talents, sharing his wealth of industry experience. His contributions have earned him prestigious honours and fellowships, including the esteemed Commander of the Order of the British Empire (CBE) and a Fellowship of the Academy of Medical Sciences.
His influence transcends the confines of academia and industry, as evidenced by his active involvement in advising governments on pharmaceutical and life sciences policy. His contributions to bodies like the UK Government’s Pharmaceutical Industry Ministerial Strategy Working Group reflect his commitment to shaping policies that foster innovation and progress in these vital sectors.
With qualifications from Calcutta Medical College and extensive psychiatric training, Professor Bhattacharyya holds a distinguished position as a Consultant Psychiatrist at South London & Maudsley NHS Foundation Trust. His research, spanning diverse methodologies from neuroimaging to epidemiological cohort studies, aims to unravel the neurobiological underpinnings of cannabis use and its therapeutic potential.
Recognized with prestigious awards including the NIHR Clinician Scientist award, Professor Bhattacharyya is committed to bridging research and clinical practice. He also leads a specialist dual diagnosis clinic, addressing the complex needs of individuals with psychosis and substance misuse. Situated within the Psychosis Clinical Academic Group at the Department of Psychosis Studies, Professor Bhattacharyya’s work underscores a dedication to advancing psychiatric understanding and treatment.
Barinder has served in various senior roles within the Government, including Director of Policy in the office of the British Columbia Premier, where he worked to ensure specific policy development aligned with the government’s broader objectives. In this role, he led a team responsible for strategic planning and cross-government coordination. As Senior Director of International Missions for the British Columbia Government, Barinder identified and led the execution of targeted international trade missions and events, ensuring missions delivered trade and investment outcomes for BC. Mr. Bhullar engaged with external parties in Canada and International Markets to encourage business to business, and business-government relationships. Barinder also served as chief of staff to the Minister of Health.
Outside of Government, Barinder was the Principal of Mainland Strategies Inc., a consultancy firm where Barinder worked with International Clients in the tech and Agtech sectors. Barinder also served as Vice President of International Affairs for a leading Health Canada licensed Canadian Cannabis Producer, leading the global market strategy for medical cannabis. In this role, Barinder worked with Governments in the UK and Brussels to provide input on Europe’s medical cannabis policy.
Chris then took up scientific roles in the pharmaceutical industry, focusing on identifying novel targets for neuropsychiatric and cognitive diseases. Chris worked for Merck, Bristol-Myers Squibb and Lundbeck. Chris was part of team that brought the antipsychotic drug Abilify (aripiprazole) to the UK market. During this time Chris retrained as a lawyer and qualified as a barrister. On completion of his legal training Chris worked in the IP team at Lundbeck, and was responsible for overseeing the IP portfolio and commercial exclusivity of the late stage and approved product portfolio. During this time Chris successfully secured the exclusivity of several of Lundbeck’s multi-billion dollar products. Chris has unique experience in using the patent and regulatory legal framework to maximise commercial exclusivity and has done cases at the European and US Patent Office, at trial and on appeal in major markets including the UK, US, Canada, Australia, Germany, Netherlands, France and Brazil.
After leaving Lundbeck Chris practised and at the English Bar and was also a partner, specialising in life sciences and IP, in London-based law firms. During this time Chris advised a range of companies, from start up to large multinational companies. Chris then joined GW Pharmaceuticals and was Vice President of IP, Head of Regulatory Law and R&D Legal and wa also a member of the R&D Leadership Team. Chris’s remit was to build an IP portfolio for Epidiolex (cannabidiol) that could provide commercial exclusivity for the product beyond initial orphan exclusivity, develop an IP strategy for Sativex (nabiximols) to prolong it’s in-market exclusivity and develop an IP strategy for the developing R&D function. Chris also established anti counterfeiting and brand protection activities for GW’s cannabinoid portfolio. GW Pharmaceuticals was acquired for $7.2Bn by Jazz Pharmaceuticals and Chris played a leading role in the transaction, which heavily focused on the IP for the GW’s medicines and pipeline. After the acquisition by Jazz, Chris remained at Jazz, and was Vice President of IP and Associate General Counsel.
Chris has a unique experience is developing and protecting cannabis based medicines, utilising innovated approaches to obtain patent protection for cannabinoid medcines, with a demonstrable record of successfully protecting cannabinoid and cannabis-based medicines. This is complemented with a deep knowledge of the regulatory framework for medicines.
Chris currently is Chief IP Officer of Pangea Botanica Ltd, which focuses on developing novel plant-based medicines and sits on the boards of Psi Pharma Ltd, Neurone Ltd and PsiClone Ltd which are developing cannabis-based medicines and psychedelic medicines for psychiatric and neurological conditions, and advises Avata Biosciences Ltd, a clinical-stage cannabinoid company.
An advocate of the research, development and prescription of medical cannabis, Damian was extensively involved in the patient-led campaigns for the UK government to reschedule cannabis-based products for medicinal use in 2018.
In 2019, Damian co-founded Kingdom Therapeutics, a team of leading experts in the pharmaceutical industry, pharmaceutical development, the science of cannabinoids, healthcare and pharmaceutical intellectual property. Kingdom Therapeutics is developing a novel cannabinoid-based medicine to help improve the lives of children living with Autism Spectrum Disorder. Kingdom’s groundbreaking science explores the role of the gut-brain-endocannabinoid axis in profound autism, and currently, their team are investigating if their first product candidate, the cannabinoid-based treatment KT-20610, can improve both behavioural and gastrointestinal symptoms in ASD.
Passionate about empowering individuals to optimize their health, Dr. Philipps guides them through lifestyle and dietary adjustments, fostering awareness and facilitating positive change. Her mission is to inspire individuals to embrace personal freedom and lead fulfilling lives.
In 2002, Dr Muhammad started a career in the pharmaceutical industry. He joined early phase Charterhouse Clinical Research and Richmond Pharmacology both in London. He worked briefly for PPD Inc before joining GW Pharmaceuticals, a UK pharmaceutical company specialized in research and development of innovative cannabinoids medicine. He worked as the medical director of GW for 6 years during which he supported several cannabinoid clinical research programmes in the company as well as helped in bringing the first cannabinoid medicine in the world (Sativex) to the market in 2010.
Dr Muhammad was trained in pharmaceutical medicine at the UK’s Faculty of Pharmaceutical Medicine (FPM) of the Royal College of Physicians as well as at the University of Wales in Cardiff from 2007 to 2011. He is honoured with the fellowships of both the FPM (the highest professional honour and recognition in pharmaceutical medicine specialty and the pharmaceutical industry) and of the Royal College of Physicians of London. His areas of expertise are in safety and pharmacovigilance of products in development and in the post-authorisation settings as well as clinical research strategies.
He has worked for many global pharmaceutical companies including InMed Pharmaceuticals (Vancouver, Canada – another cannabis medicines research and development company), Ipsen, AstraZeneca, UCB, IO Biotech and Cybin in various capacities including as a chief medical officer, vice-president and senior global medical director helping these companies to develop and register several neurology, oncology and other products iglobally. He has also consulted for regulatory authorities, helping to draft guidelines, conduct training and inspections.
Dr Muhammad holds a specialist MBA in pharmaceutical industry management and is a current board member of the FPM.
Apart from Pharmaceutical Medicine practice, Dr Muhammad is a keen global health enthusiast with special interests in the areas of drug development for neglected and rare diseases, planetary, environmental and social determinants of health. He acquired a postgraduate degree in global public health from Queen Mary’s University of London and is a fellow of the UK’s Faculty of Public Health.
Clarissa is a qualified solicitor in England and Wales with experience in the retail, telecoms, and pharmaceutical sectors. Following an early career with Penningtons Manches Cooper LLP in London,
where she spent time seconded to a range of clients including London Underground Limited and All Saints Retail Limited, she held posts as senior in-house counsel in established corporations including Hutchison 3G UK Limited (Three) and Virgin Media Limited, a subsidiary of Liberty Global plc. She is a member of ICSA, The Chartered Governance Institute. Clarissa is also a management coach and has delivered compliance training and management coaching to blue chip clients including Google LLC, Biogen Inc. and McDonald’s Corporation across the EMEA and APAC regions.
Clarissa holds a BA in philosophy and literature from Warwick University and PGDL and LPC from BPP Law School in London. After completing her undergraduate degree, Clarissa spent two years working as a project manager in the residential construction industry before retraining as a solicitor.
His expertise includes managing key multi-billion-dollar products like CRESTOR®, FORXIGA®, and KEYTRUDA®. At Artelo, Dr. Yates is tasked with advancing the company’s research and development, overseeing engagement with the Scientific Advisory Board, and contributing to the executive management team. His focus lies in developing therapies for anorexia, cancer, PTSD, pain, and inflammation, showcasing a commitment to addressing significant unmet medical needs.
Dr. Yates is known for his successful track record in partnership agreements with academia, biotechnology, and pharmaceutical companies, highlighting his collaborative approach to advancing healthcare solutions.
