About us
Who we are
Established in 2006, Guy Howland Ltd provide specialised scientific technical writing services to a worldwide client base within the in vitro diagnostic, medical device and pharmaceutical industries.
Rapid, responsive, reliable
Our team put the values of rapidity, responsiveness and reliability at the heart of everything we do and embody them in how we interact with our clients and with each other.
UK based
Customers worldwide
Established 2006
Meet the team
Our team consists of highly qualified and motivated scientists, supported by an agile management team, who are passionate about what they do.
Combining many years' experience of the in vitro diagnostic, medical device and pharmaceutical industries with wide ranging expertise across academia; our people have the expertise to provide rapid, reliable and responsive technical writing services to fully meet our client's necessarily demanding requirements.
Founder & Director
Guy Howland
Guy is the Founder and a Director of Guy Howland Ltd, an established UK-based company specialising in writing services for the in vitro diagnostic (IVD), medical device and pharmaceutical industries.
With 40 years of experience within the healthcare sector, Guy has held senior positions across central government and within the public, private, and voluntary sectors. Guy specialises in advising and providing written support to Chairs and Chief Executives of healthcare and allied companies.
Lead Medical Writer & Director
Jane Leadsham
Jane is a Director of Guy Howland Ltd and a published scientific writer. Jane holds the position of Lead Medical Writer within the company, bringing a wealth of scientific expertise to bear on the written technical evidence which supports complex IVD, medical device and pharmaceutical products in, and about to enter, global markets.
With a Ph.D in Biochemistry and a BSc in Cellular and Molecular Biology, Jane possesses over 20 years of laboratory bench-based experience in scientific research; including extensive cross-sector experience within academia, a successful biotechnology startup and a Top 10 global pharmaceutical company.
Medical Writer
Vicky Murfitt
A Senior Scientist with over 20 years of experience within the pharmaceuticals industry, Vicky holds an MSc in Medical Diagnostics and BSc in Physiology & Biochemistry.
She has been involved in point-of-care IVD device development, within a small biotech start up, through acquisition and expansion by a major Top 10 pharmaceutical company. Additionally, Vicky has undertaken assay development from initial feasibility studies, through development into verification and validation for commercial product release.
Medical Writer
Lynsey Mills
A Senior Analytical Chemist, Lynsey brings a demonstrable history of working in the pharmaceutical and medical device industries within ISO13485 accredited laboratories.
Holding an MSc in Analytical Toxicology, she is an experienced and conscientious analytical and research professional, with extensive experience of laboratory work and the production of Quality and Analytical technical documentation.
Junior Medical Writer
Winston Tang
A Scientist and Project Manager with extensive experience in the bioanalytical field, Winston holds a BSc in Biomedical Sciences.
He has supported the development of innovative and effective medicines through his data analysis and research expertise, working within Top 10 global pharmaceutical and life science companies.
Business Support Manager
Alan Burdon
Alan is a versatile manager with a wealth of cross-sector experience acquired in the financial services, business process outsourcing, and regulatory compliance domains.
He has worked within a diverse range of organizations, spanning from multinational corporations to small and medium-sized enterprises.
20 years
Research Experience
20 years
Management Experience
20 years
Cross-sector Experience
Partner with us
Connect with us to access support tailored to your technical scientific writing and associated international and national regulatory body needs (e.g.: Notified Bodies in the EU or UK and FDA in the USA).
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