3D Communications

For more than 20 years, 3D Communications has prepared pharmaceutical, biotech, and medical device companies for high-stakes interactions with US and EU regulatory authorities - helping them build the skills they need to communicate effectively.

3D’s science, regulatory, communications, and market access experts leverage their proven 3D ACT® process and state-of-the-art technology to help clients transform complex information into clear and convincing messages and presentations—and deliver with confidence and purpose.

Arriello

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

Billev Pharma East ensures your products and GxP systems are always compliance-ready. Since 2007, we’ve actively contributed to shaping new legislation through international organizations, allowing us to offer consultancy services that stay ahead of regulatory changes. Our growth is fueled by loyal clients who trust us to navigate the complexities of the regulatory landscape. Partner with us for expertise and forward-thinking solutions that keep you confidently aligned with the latest industry standards.
 

Biomapas

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. .

EXTEDO

EXTEDO is a leading provider of Regulatory Information Management solutions, optimizing eRegulatory processes across content, quality, product registration, submission, and safety management. By streamlining these processes, EXTEDO helps both industry and agencies navigate regulatory challenges with greater efficiency. Today, EXTEDO serves over 1,000 clients and 35 regulatory authorities globally, ensuring compliance throughout the lifecycle of medicinal products.

Fera Science

Fera Science is participating in the TOPRA Symposium to forge new connections in the human health and veterinary medicine sectors. With a track record of supporting clients in environmental risk assessments, Fera collaborates closely to diminish risk quotients and refine PEC values, contributing to the successful registration of novel products. The TOPRA Symposium presents a valuable platform for Fera to stay informed, engage with industry professionals, and further strengthen its commitment to effective environmental risk management.
 

GMED

GMED and its subsidiaries (GMED North America, LNE-GMED UK, and GMED Asia) support manufacturers of medical devices (MDs) and in vitro diagnostic devices (IVDs) in certification projects, regardless of product risk or technology. As a notified and certification body, GMED is internationally recognized for its expertise in MD conformity assessment and QMS (CE marking, MDSAP, UKCA). It also provides technical/regulatory resources, training, webinars, and forums to assist customers in achieving their MD marketing goals.
 

IQVIA

Partner with IQVIA for your regulatory strategy, lifecycle maintenance, publishing, intelligence, and language needs supported by Healthcare-grade AI™, from early drug development through submissions and post-registration. Free your team from labor-intensive regulatory tasks and maintenance to focus more on delivering valuable products to market.
 

Parexel

Parexel is among the world’s largest CROs, providing full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, we collaborate with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials for patients. We work With HeartTM every day to treat patients with dignity and learn from their experiences, so every trial makes a difference.
 

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.

Vivpro

Discover the future of biotech and pharmaceutical decision-making with Vivpro. Our cutting-edge bio-intelligence software platform empowers industry leaders with lightning-speed insights for evidence-based clinical, regulatory, and business strategies. Revolutionizing how pharmaceutical, biotech, and medical product companies operate, we fuse technology with expertise to navigate complex challenges effortlessly. With our R&D Intelligence Assistant (RIA), craft-winning product strategies with faster decisions, superior strategy and better quality! ;