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.



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.



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.


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™ And our statement why we have decided to take a stand at the Symposium “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.

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.


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.



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.




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.




Scendea is a leading product development and regulatory consulting practice serving the pharmaceutical and biotechnology industry. We offer strategic and operational support in the fields of quality/CMC, non-clinical/toxicology, clinical/medical, and regulatory, to guide products efficiently from early development to marketing approval.

Our industry experience is demonstrable, having been involved in over 1,000 development programmes in the US and Europe over the last twenty years. As is our scientific excellence, with an international team that includes ex-regulators, high-calibre academics, and clinician scientists.


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.


Trilogy Writing & Consulting

At Trilogy, medical writing is our passion. As specialists in regulatory documentation, we provide a service that is more than just writing. Our writers are integral parts of our clients’ teams. We proactively plan, coordinate and write regulatory documents to meet timelines, with a readability that reduces the time for review and approval. Our goal is to help teams streamline their documentation process and make sure their documents communicate clearly and effectively.


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