Gold Corporate Sponsorship:

ZYLiQ is going to give medical writers what they need… time. No more spending weeks creating Clinical Study Reports (CSRs), Medical Writers can now use their valuable time on interpretation of study results and their discussion points.

The premise is simple... Using AI, ZYLiQ allows users to automatically generate CSRs (according to ICH E3 guidelines) that would otherwise take days or months even.  The tool allows for easy Post-Text to In-Text table generation, with interpretation of tables, Synopsis summarization, automatic tense conversion, multi-authoring, consolidated view of reviewers comments and more.

ZYLiQ also has robust workflow functions, traceability reporting as well as a complete audit log.  Let ZYLiQ accomplish the tedious manual “copy/paste” aspects of a CSR and allow you to complete the report accurately and efficiently, in days instead of weeks.

Bronze Corporate Sponsorship:

For more than 135 years, Johnson & Johnson (the “Company”) (NYSE: JNJ) has provided health care products and solutions to people worldwide.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. 

Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Our diverse portfolio spans multiple therapeutic areas—Oncology, Immunology, Neuroscience, Cardiovascular, Pulmonary Hypertension, and Retina. We are continuously working to develop treatments, aspiring to find cures, pioneering the path from lab to life, and championing patients every step of the way. Patients inform and inspire our science-based innovations, which continue to change and save lives.

Learn more at https://www.jnj.com/.

Parexel is among the world’s largest clinical research organizations (CROs), providing the 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, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com and follow us on LinkedIn, Twitter, Facebook and Instagram. 

Conference Sponsors:

ALBION RYE ASSOCIATES

Albion Rye Associates are one of Europe's leading Medical Writing staffing partners. Specialising in working with Medical Writers focused on Regulatory Writing, Publications, Medical Affairs, Medical Education, Market Access and Technical Writing.

Offering bespoke staffing solutions to our clients and candidates, we support a range of Pharmaceutical, Biotech, CRO, Medical Device & Consulting business make strategic appointments.

Working across Permanent, Freelance, Retained Searches & Full Team / Project Hires, Albion Rye Associates truly are the go-to staffing partner for Medical Writing talent.

Certara accelerates medicines using proprietary biosimulation software, technology and services that transform traditional drug discovery and development. Its clients include more than 2,000 biopharmaceutical companies, academic institutions and regulatory agencies across 62 countries. 

Introducing OnStyle - the game-changing add-in for medical writers. Say goodbye to inconsistent and inaccurate work with this intuitive and user-friendly tool that seamlessly integrates with Microsoft Word.

OnStyle offers a wide range of features designed to make your writing more professional, while also significantly speeding up document authoring.

With OnStyle, compliance with predefined formatting standards is a breeze, as it automatically identifies and fixes compliance issues, ensuring consistent PDF rendering.

Spend your time on content creation and rely on this extremely powerful tool to produce submission-ready documents faster and more efficiently than ever before.

DACHS is proud to deliver unique document management solutions and services to meet the demanding pharma regulatory requirements.

Don't miss your chance to see OnStyle in action and learn how it can revolutionize your medical writing process. Visit our booth at the conference and discover how OnStyle can take your writing to the next level.

Ideagen PleaseReview enables secure real-time document review, co-authoring and redaction in order to shorten the document review process by up to 65%. The collaborative platform simplifies the creation and review of regulatory filings, including INDs, NDAs, protocols, CSRs and other critical documents. Used by medical writing teams across the world, Ideagen PleaseReview your key to accelerating regulatory approval processes and expediting timelines to bring therapies to market faster.

The fully validated software facilitates real-time collaboration among internal and external reviewers, allowing for simultaneous edits and comments, thus expediting the document's completion while maintaining version control and document formatting. Its intuitive interface simplifies the review process, enabling users to provide feedback effortlessly, track changes, and resolve discrepancies efficiently.

Moreover, Ideagen PleaseReview integrates with existing software such as Veeva Vault, Generis CARA, Opentext Documentum, InteliNotion and Ideagen Quality Management, thus enhancing workflow integration and ensuring data security. By leveraging Ideagen PleaseReview, medical writers can optimize their document review workflows, leading to improved productivity, reduced errors, and ultimately, enhanced quality in medical publications and regulatory submissions.

At Trilogy, medical writing is our passion. As specialists in regulatory and safety documentation, we provide a service that is more than just writing. Our writers are integral parts of our clients’ teams: proactively planning, coordinating and writing their regulatory documents to meet timelines, with a readability that reduces the time for review and approval.

We have been helping pharmaceutical companies and clinical research organizations of all sizes, worldwide, to streamline their documentation processes for over 20 years – either as support on a one-off document or the entire clinical development program. We pride ourselves on our team approach when developing documents, which greatly reduces the time needed for production and ensures much greater levels of continuity throughout an entire development program.

Trilogy currently employs more than 80 medical writers. We have writers in 7 countries worldwide, with 3 physical offices: Frankfurt, Germany (HQ); Cambridge, UK; and Durham, North Carolina, US.

 

Symposium Media Partner:

The Publication Plan is a free central online resource delivering up-to-date news on key issues for everyone in the medical publications industry. Every week, we curate and deliver the latest industry updates via our website, email alerts, Facebook, Twitter and LinkedIn. Our dedicated global readership already includes medical writers, publication planners, researchers, pharmaceutical industry members, medical journal editors and publishers.