BSI (British Standards Institution) has over 81,000 clients in 180 countries and is an organisation whose standards inspire excellence across the globe. BSI Medical Devices Notified Body provides rigorous CE and ISO 13485 certification to manufacturers globally. Our teams apply their knowledge to 3rd party conformity assessment of all types of medical devices; active devices, active implantable devices, in vitro diagnostic devices, orthopaedic and dental devices, vascular devices, wound care devices and many others.



DLRC logo DLRC is a leading Regulatory Affairs consultancy employing more than 70 Consultants with offices located in United Kingdom and Germany. Our dynamic and award-winning team provides comprehensive regulatory affairs services from strategic advice in early drug development, to compilation and management of regulatory submissions . With high quality at the heart of our business, since 2005 DLRC has helped companies of all sizes to maximise the commercial value, timely marketing of their products and ensuring our clients are set up aligned to the new regulations such as CTR and MDR.


DWL – Dora Wirth Languages

DWL logoIn house medical expertise, a proven track record of dedication to the field, and a strong commitment to quality and service all combine to make DWL your reliable partner for global life science translation solutions. DWL has over 55 years’ experience in providing translation services in the following specialist areas: regulatory affairs, clinical research, medical devices, medical research, medical publishing, manufacturing, legal, and marketing communications.

ONIX Life Sciences

Onix Life Sciences logo ONIX offers industry-led expertise and guidance to help Pharmaceutical, Biotechnology, Generic, Herbal and Medical Device companies fast-track their journey to regulatory approval via eCTD Submissions. Our experience ensures high quality and avoids costly pitfalls by operating as an extension of your regulatory team. We specialise in Regulatory Operations Strategy, Submission and Lifecycle Management by following processes and using Templates and Style Guides while adhering to ICH and Regional requirements. We know eCTD and hit the ground running, working as a team to bring our vast experience to each project. ONIX focuses on helping clients get their documents submission ready and do it right first time every time with ONIX CTD templates. From our 20 years plus of Submission experience we understand what could wrong with complex documents so are well placed to spot and avoid potential issues. Our goal is to solve our clients’ document problems to free them up to focus on what matters.



Pharm Assist

Pham Assist logo Pharm Assist is a consultant and service company offering regulatory solutions for pharmaceuticals and medical devices since 1996. A highly qualified team with a strong scientific and regulatory background provides customised services in Regulatory Affairs, Pharmacovigilance, Medical Writing and Quality Assurance to national and international companies.



Pharmalex PharmaLex supports pharma companies throughout the entire product lifecycle, ensuring compliance with pharmaceutical regulations and providing vital scientific and strategic advice on drug development. Our services extend beyond market approval and include product maintenance post launch activities. PharmaLex differs from other providers by focusing on specialised regulatory services (rather than clinical ops, manufacturing or sales support) to deliver and comply with all health agency obligations. Our global team has more than 850 local knowledge experts.

Pharmiweb is Europe and Australia’s Largest Pharma Job board. With over 3,000 live jobs from the key players in the Life Science industry, is the best place to find your next role. Search now or upload your CV and let the jobs find you! Our clients benefit from a CV Database, Employer branding training and market insights. Come and see us today and see what PharmiWeb can do for your business.


ProductLife Group

ProductLife Group specialises in helping international life sciences organisations more effectively get their products and therapies to market by providing those clients with functional support across all of the regulated stages of the product life cycle – from development to launch to postmarketing.


TOPRA Symposium 2021

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