How Can Advisory Boards Translations Help Pharmaceutical Companies?
Advisory Boards Translations ensure that pharmaceutical companies maintain regulatory compliance across borders and meet language needs for advising talent around the world. Advisory Boards constitute a body of Key Opinion Leaders (KOLs) providing valuable non-binding insights to a pharmaceutical/biotech company on a product or a disease state.
This provides guidance on product development strategy, deeper insight into disease epidemiology, guidance on interpreting trial outcomes and developing patient outreach programs, and directs future healthcare strategy.. The advisory board may include diverse stakeholders, such as healthcare practitioners, patients or patient advocates, payers, as well as external experts and influencers, with the number of advisors ranging from eight to fifteen.
The advisory board provides pharmaceutical companies deeper insights into unmet medical needs, as well as drives a deeper level of engagement with the medical, scientific, and patient communities. While there are open and insightful discussions, it is important to have well-defined goals for the advisory board meeting, led by an experienced moderator who can drive clear, actionable outcomes.
- Working with the sponsor to develop the agenda and defining the outcome for the meetings
- Helping identify KOLs and sending out invitations to them
- Organizing the logistics,including the procurement of venue and transportation resources for KOLs
- Hostingthe event virtually/on-site
- Procuring content developers and graphic designers for slide deckcreation
- Moderating the advisoryboard and recording meeting minutes
- Providing translators/interpreters to support intercultural communication in the meeting
- Providing the final summary report of the meeting
Pharmaceuticals Translations
With the global pharmaceuticals sector currently valued to be over a trillion-dollar industry, demand for pharmaceutical translations has expanded to both domestic and foreign markets, enabling substantial growth through multilingual clinical trials and with predicted estimates to be even more profitable in the future. Beyond medico-marketing materials, the growing overseas demand for drug therapies and treatments means that pharma companies need to ensure that clinical trial documentation and regulatory documents are translated with the highest degree of accuracy and quick turnaround times; doing so not only prevents companies from potentially endangering patient lives, but also from losing millions of dollars for failing to comply with regulations.
CSOFT Health Sciences’ global network of over 10,000 in-country linguists and subject matter experts provides the highest-quality pharmaceutical translation services for all stages of the drug lifecycle in 250+ languages, from CTD/eCTD submission and phase 0-IV to clinical trial documentation to pharmacovigilance reports and medico-marketing materials.
Learn more about our pharmaceuticals translations.
Complete Translation Coverage for An Extensive Range of Therapeutic Areas
CSOFT Health Sciences’ medical translation and localization coverage expands across a full range of clients, therapeutic areas, and treatment settings. Whether your advisory board focuses on pharmaceutical products in oncology, immunology, and neurology, or specializes in rheumatology, genetic diseases, or women’s health, CSOFT’s end-to-end localization support covers an extensive range of conditions and therapies across disciplines.
Learn more about our comprehensive coverage for therapeutic areas here.
Quality Assurance
CSOFT Health Sciences has developed a process for quality assurance to ensure that every medical translation project meets quality standards in a cost-effective and timely manner. We are certified in ISO 17100:2015, ISO 9001:2015, and ISO 13485:2016 to ensure our customized solutions meet global regulatory requirements. Our subject matter expert linguists have a minimum of 7 years’ experience and work with in-country reviewers and project style guides to meet industry standards. And through our innovative cloud-based technology, CSOFT offers an online translation management ecosystem for one central location to leverage both translation memory as well as terminology management in real time. Every step of the way, CSOFT has you covered.
Learn more about our quality assurance process.
Data Security
With over 20 years of experience in medical translation, CSOFT Health Sciences understands the importance of data security to our clients, and we take nothing for granted when confidentiality is a concern. Our well-documented and fully traceable information data security policies, checklists, and quality records leverage best practices of ISO 27001, and are designed to keep everything from source data to translations protected. From our 24/7/365 data monitoring and advanced encryption to our access control measures, you can be certain that your project data is safe from start to finish.
Learn more about how CSOFT prioritizes data security.