Endpoint Adjudication Translation Practice

Streamline endpoint adjudication with fast, AI-optimized translations. Our rigorous quality process ensures precision and compliance, empowering your clinical experts to make informed decisions confidently on a global scale.

Endpoint Adjudication Translation Services

Language Scientific has over 20 years of experience providing clinical translation services. We specialize in high-quality expedited turnaround Endpoint Adjudication translation and source case endpoint adjudication translation icondocuments translation for global clinical trials. Language Scientific employs translators who are M.D.s, experts at translating materials written by other doctors and working with clinical trial source documents that may be either poorly scanned or handwritten. Throughout the translation process, Language Scientific takes these handwritten or typed clinical documents and recreates them in an electronic format. Language Scientific’s Endpoint Adjudication translation practice is able to customize the workflow to fit your specific clinical translation needs.

Translation Capabilities

Regulatory

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  • Specialized in translating regulatory compliance documents for medical and surgical devices.
  • Expertise in translating EU and Asian market regulations.
  • Support for package inserts, labels, and other crucial documents for regulatory approval.

Clinical

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  • Comprehensive translation for clinical trials and research protocols.
  • Translation of Development Safety Update Reports (DSURs) and Suspected Unexpected Serious Adverse Reactions (SUSARs).
  • Support for translating case report forms, patient consent forms, and clinical study reports.

Marketing

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  • Adapt marketing materials with a focus on cultural relevance and impactful messaging.
  • Specialized transcreation services to ensure your brand resonates with global audiences.
  • Translation of brochures, promotional content, and digital campaigns

Operations

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  • Expertise in translating manufacturing process descriptions for medical devices.
  • Translation of standard operating procedures and maintenance manuals.
  • Comprehensive support for global operational documents to ensure accuracy across markets​

Language Scientific’s Key Focus Areas

Specialized Endpoint and Pharmacovigilance Translation Practice:

  • Dedicated Clinical Trials Practice Group
    • Rapid and expedited customized processes
    • Leveraging technology for real time submission & translation
  • Doctors, nurses & medical professionals decipher and translate Source documents
  • Flexibility (we flex for you not vice versa)
    24 hour resources enable accurate, quick and cost reducing whenever possible
  • Detection of duplicate files submitted from multiple sites, saving our clients significant money and time.
  • Redaction services, ensuring that no Patient Identifying Information is submitted (both in the source and target documents)

Why Choose Language Scientific for your Endpoint Adjudication Translation Needs?

At Language Scientific we specialize in clinical translation, with a special focus on translation for Endpoint Adjudication. Our dedicated Endpoint Adjudication Translation team works with our clients to fit in with your current workflows.

  • Medical materials translated by doctors, edited by linguists
  • No PM fees or hidden fees, complete pricing transparency
  • 99.5% of projects completed by promised deadline
  • Linguists are tested and accredited by language pair and subject matter expertise
  • Project Manager response time < 2 hours

The typical documents we translate for our Clinical Industry clients include:

  • Adverse Event Source Documents
  • Case Report Forms (CRFs)
  • Data Sheets
  • Development Safety Update Reports (DSURs)
  • Dossiers
  • Drug Registration Documentation
  • Endpoint Adjudication Documents
  • Informed Consent Forms
  • Insert Leaflets
  • Instructions for Use (IFUs)
  • Marketing Collateral
  • Master Batch Records
  • Package Inserts and Labels
  • Patient Diaries
  • Patient Recruitment Materials
  • Patient Reported Outcome Measures (PROMs)
  • Patient Source Documents, Admission and Discharge, Labs
  • Pharmacological Studies
  • Product Labels
  • QoL Scales
  • Regulatory Documents
  • Scientific Papers
  • Study Protocols
  • Suspected Unexpected Serious Adverse Reactions (SUSARs)
  • Toxicology Reports

The Role of AI in Medical Device Translation

AI is redefining technical translation by ensuring accuracy, speed and regulatory compliance across your projects. Our AI-optimized translation solutions streamline the translation of complex technical documentation, enabling clear communication across the globe. By combining AI efficiency with expert human review, technical organizations can deliver precise, reliable translations that meet the highest standards for regulatory compliance.