2023 Exhibitors

3D Communications

3D Communications is a leader in healthcare communications that specializes in preparing pharmaceutical, biotech, and medical device companies for high-stakes communications, including US and EU regulatory meetings and interactions. We transform complex data and information into clear, credible, and compelling communications that can be delivered authentically, confidently, and with purpose. Our world-class science and communications experts leverage our proven 3D ACT® process and state-of-the-art technology to drive communication excellence in the most challenging situations.


ACHIEVA, a renowned leader in total talent solutions for over 30 years, excels in sourcing industry experts across diverse specialist sectors within the life science industry. With offices in the UK and Switzerland and a focus on regulatory affairs professionals within medical device, pharmaceutical, biotech spheres, ACHIEVA covers a wide range of disciplines from clinical trials to registrations and post-marketing. Embracing change as an avenue for immense opportunities, ACHIEVA benefits both clients and candidates alike. Discover your potential with ACHIEVA's tailored talent solutions.


Argenta: advancing animal health from molecule to market. Founded in 2006, we have built our reputation and expertise on a singular focus: animal health. To this day, we are the world’s only combined global contract research organisation (CRO) and contract development and manufacturing organisation (CDMO) specialising in animal health. From beloved companion animals to farm animals, when their lives are made better, we're all better for it. 


ArisGlobal is transforming the way today’s most successful Life Sciences companies develop breakthroughs and bring new products to market. Our end-to-end drug development technology platform, LifeSphere®, integrates our proprietary cognitive computing engine to automate all core functions of the drug development lifecycle. Designed with deep expertise and a long-term perspective that spans more than 30 years, LifeSphere® is a unified platform that boosts efficiency, ensures compliance,
delivers actionable insights, and lowers total cost of ownership through multi-tenant SaaS architecture.

Headquartered in the United States, ArisGlobal has regional offices in Europe, India, Japan and China.


Arriello is a leading consultancy and solutions provider of risk management and compliance services to the pharmaceutical industry. They have been making the development-to-market process faster, better, and smarter since 2008.

Their global services span the product life cycle from Clinical to post-submission Regulatory Affairs and Pharmacovigilance, Quality Assurance and Auditing, and innovative automation solutions. Valued clients rely on their ability to deliver, however complex their requirements, through their proven expertise, global coverage, and technology. 

Billev Pharma East

With a mission to ensure your PRODUCTS and your GxP systems are in compliance, it has been their vision to be early in providing assistance with the growing amount of new legislation through active participation in the preparatory work for rules and regulations through international organisations.

Through diligent consultancy work, Billev Pharma East has since its beginning in 2007 slowly grown to its present size also because of loyal customers. This is what has enabled us to provide fully up-to-date consultancy to their customers.


biologit MLM-AI is a scientific literature monitoring platform for active safety surveillance that is simple to use, fully web-enabled and powered by AI. Our validated and compliant platform offers true productivity gains and is ready for pharmacovigilance and safety screening for medical devices, cosmetics or veterinary products.

Their mission is to develop technology to enable users enjoy, learn, and more efficiently deliver meaningful results that improve safety and prevent harm. And their vision is to help keep patients safe by simplifying the detection of risks and events from development to post-market.


Biomapas is a premier contract research organization (CRO) delivering flexible solutions globally throughout development as a seamless extension of your team. Our colleagues spread through all European, Commonwealth of Independent States (CIS), Eurasian Economic Union (EAEU) and Middle East/North Africa (MENA) regions can enhance your drug development, accelerate your path to market authorization, and ensure compliance with local and global post-marketing requirements. we do so through a complete service scope in clinical research, regulatory affairs, pharmacovigilance, and medical information.


Canopy (Formerly ONIX Life Sciences Ltd) provides clinical to commercial solutions to over 225 biotechnology, pharmaceutical, and medical device companies. The company offers consulting and operational support services in the areas of Regulatory Affairs, Regulatory Operations (eCTD, CTIS/CTR), Medical Affairs, MLR, Technology, and Global Recruiting


DLRC is an award-winning, leading Regulatory Affairs consultancy employing more than 80 consultants with offices in the United Kingdom and Germany.

Our experienced team provides comprehensive strategic and operational support to the pharmaceutical, biotechnology, medical technology, and related industries. DLRC specialises in supporting the development, approval, and commercialisation of healthcare products across the major markets including EU, UK, and USA.


DWL is the Life Sciences division of the fastest growing Language Service Provider (LSP) in the world – BIG Language Solutions. With 60 years of experience, DWL provides language solutions to leading Life Sciences organisations in the pharmaceuticals and medical devices sectors as well as academia and clinical research. Our specialist global supply chains are underpinned by in-house medical expertise. DWL supports your business goals through language services which are unified, effective and secure.


Too busy developing new products to deal with old products licenses updates? No time to evaluate precisely the risk, time and money involved in expanding existing approvals beyond the base indications and geographies of the initial product characteristics? EOVET is assisting veterinary pharmaceutical companies in maintaining, defending, or extending their veterinary products registrations globally. You simply submit your needs and our experts will design a free feasibility study.


Essenvia is a US-headquartered tech company that provides innovative MedTech regulatory solutions. Our flagship product, the Essenvia Platform, is an innovative SaaS product designed to simplify the regulatory submission process for MedTech regulatory submissions. Across the globe, regulatory affairs teams are using Essenvia to save time and reduce stress when managing their submissions.


EXTEDO is a leading solutions and services provider in the field of Regulatory Information Management (RIM). We focus on optimizing our clients’ eRegulatory business processes and provide solutions covering the entire regulatory landscape. Today, EXTEDO enables more than 35 regulatory authorities and over 1000 maintained customers across 65 countries to deliver Effortless Compliance™. The TOPRA symposium is a great opportunity for us to meet with our industry and agency customers, partners and other experts from around the world and to exchange information on the latest trends and challenges in regulatory information management.


Fortrea is a leading global provider of clinical development and patient access solutions to the life sciences industry based in 90 countries, leveraging three decades of experience through multiple therapeutic areas. We partner with emerging and large biopharmaceutical, medical device, diagnostic companies to drive healthcare innovation that accelerates life-changing therapies to patients. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions, regulatory strategy consultancy and post-approval services. 

G&L Healthcare Advisors

G&L Healthcare Advisors uses subject matter expertise and decades of experience gained in every aspect of Regulatory Affairs, Quality Assurance and Clinical Development to meet the challenges faced by healthcare companies globally. From product development and submissions to company-wide change management, they design, implement, and run quality, results-focused outcomes for all our clients. Their innovative solutions and services support clients at all stages of development to deliver meaningful change for the better.

Kinesys Consulting Ltd

At Kinesys, we pride ourselves on our dedication to premium quality services and responsiveness to our clients. Kinesys provides global Regulatory Strategy & Submissions, Regulatory / Scientific Writing, and Medical Device consultancy. Established in 2007, Kinesys supports product developments through to MAA and beyond for a wide range of US and European pharma and biotech companies, across most therapeutic areas and product types (NCEs, biologics, ATMPs). Visit us at Stand 23.


MedBoard is the Regulatory, Research & Intelligence platform for MedTech, Digital Health, and Pharma. It provides a new exceptional access to up-to-date global information in the areas of Regulatory (225+ countries), Standards, Clinical, Market and PMS; covering News, Databases & Analytics, Profiles, Intelligence, and Tools.

The MedBoard Search (1Billion+ datapoints) and Content, AI powered, are embedded with powerful digital Enterprise Solutions such as Systematic Reviews, Lists Monitoring, Product Portfolio, RIM Country Registrations, Task Manager, Compliance Portfolio and more. MedBoard is a multi-use platform, widely used by many leading organizations for Regulatory Intelligence, Literature Reviews, PMS Automation, Country Registrations Management and Market/Clinical Research.


NSF provides a comprehensive range of support services for the pharmaceutical, medical device/IVD, and nutritional supplements industries covering consulting, training, and auditing on a global basis.

Their team of ex-regulators and renowned industry experts work with companies around the world on Global Regulatory Affairs; GMP Readiness Audits & Mock Inspections; QMS & Compliance Support; Enforcement Support & Remediation; and Training & Education Solutions.


PharmaLancers is the global marketplace to connect independent consultants in regulatory affairs, medical writing, pharmacovigilance, biostatistics, project management and medical communication services to relevant projects and assignments with the global pharmaceutical, biotechnology and life sciences industry. If you are a freelance consultant, PharmaLancers does all the hard work for you. The marketplace will match and connect you to companies who are looking for expert help from consultants like you. For companies, PharmaLancers will help you to find the best independent and fully vetted consultants to support your projects.


PharmiwebPharmaLex 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 PharmiWeb.jobs is the world’s largest Life Science Job board. With over 5,000 live jobs from the key players in the Life Science industry, PharmiWeb.jobs is the best place to find or advertise your next role. Search PharmiWeb.jobs now or upload your CV and let the jobs find you! Our clients benefit from a CV Database, Employer branding training and market insights. Contact us today and see what PharmiWeb can do for your business.



PPi Healthcare Consulting Ltd

PPi HC Ltd is a health technology pricing, reimbursement (P&R), HTA and market access specialist comprising an international team of country-based experts intimate with their respective healthcare systems and very familiar with commercialisation requirements and considerations for pharmaceutical and health technology products.

PPi HC works closely with Regulatory Affairs and Communications agencies and partners to provide clients with a cohesive suite of specialist services which address all the challenges of securing fast and revenue-optimizing market access.


For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.

QbD Group

The QbD Group supports life science companies worldwide throughout the entire product lifecycle – from idea to patient. Since 2011, it has been providing quality solutions for product development and manufacturing. 

The team offers the skills and expertise for solving complex project problems in quality assurance, validation & qualification, regulatory affairs, clinical, quality control, software solutions and go to market for companies active in the biotech, small molecules, digital health, medical device & IVD industries.

QbD Group is headquartered in Belgium and has over 450 consultants worldwide in the Netherlands, Spain, France, UK, Switzerland, Mexico, Colombia and the US.


DLRC logoRapport is a regulatory and product development consultancy with a team of highly experienced experts, including ex-Regulators from across the globe to provide innovative solutions to global programmes. We have a flex model, providing strategic and tactical support for specific programmes or issues, or we can integrate into your team, building your core capabilities. RApport has a proven track record on delivering successful drug/device development, including designing CMC, non-clinical and clinical programmes, preparing robust risk registers and mitigation plans including a Strategic Advisory Panel service (AdvizON), all of which has helped inform clients to identify accelerated pathways to drug/ device approval.


regulanet® is a global network of qualified independent consultancies with expertise in development, regulatory, market access, and lifecycle management in 90 countries around the world. Founded in 2001 by regenold GmbH, regulanet® consists of over 120 individual and partner organisations providing expertise in specific topics to a wide variety of national and international healthcare and pharmaceutical clients. We listen, collaborate, and offer advice based on years of experience and can support all facets of development.

Schlafender Hase

Schlafender Hase delivers an easy-to-use document comparison software for regulatory affairs to reduce the time you spend proofreading. Our solution, TVT®, catches even the smallest differences, ensuring that only approved content is printed or published. Easily verify text, artwork, barcodes and spelling.

Designed for and proven within the highly regulated life science industry, TVT is currently used by 20 of the top 20 life science companies and standardized globally by 13 of the top 20.

TransPerfect Life Sciences

TransPerfect Life Sciences specializes in supporting the global development and commercialization of drugs, treatments, and devices designed to improve and save lives. Our comprehensive solutions include clinical trial management technology and services (TMF services, eTMF, CTMS, pharmacovigilance and safety solutions, translation services, and call center support. With offices in 100+ cities , TransPerfect is the ideal partner to ensure your global launch makes a global impact by driving quality, mitigating compliance risk, and enhancing patient engagement.


Veeva is the global leader in cloud software for the life sciences industry. Committed to innovation, product excellence, and customer success, Veeva serves more than 1,000 customers, ranging from the world’s largest biopharmaceutical companies to emerging biotechs. As a Public Benefit Corporation, Veeva is committed to balancing the interests of all stakeholders, including customers, employees, shareholders, and the industries it serves.


Yseop is the leader in Generative AI for regulated industries and act as an content automation AI-powered digital copilot for medical writers, maximizing their efficiency and accuracy in generating reports and insights. With a suite of industry-specific applications and cutting-edge technology, we ensure that even the most demanding content automation tasks are met with ease, scalability and application security across the entire enterprise. Yseop Copilot allows you to reimagine the future of medical writing with Generative AI.

TOPRA Symposium 2023
Lisboa Congress Centre, 
Praça das Indústrias 1,
1300-307, Lisbon, Portugal

Contact us
+44 (0)20 7510 2560


Exhibition / Sponsorship
Call +44 (0)20 7510 2573
or email erik@topra.org