With effective and value-abiding translations, it gets easier for a pharmaceutical company to meet the market’s regulatory standards and expectations. A successfully constructive translation enables a business to achieve faster approval for their medical and health products. Ulatus has been serving companies in the heavily regulated life science industry, with accurate and high quality translations. We have been providing translations with highest quality and precision to various segments: Healthcare, Pharmaceutical, Biotech, Medical Devices, and more. Having a dedicated expert team enables us to deliver regulatory translations with high standards for both medical and health products.This team of translators also holds an extensive industry experience of working with regulatory agencies like FDA, EMA, CFDA, and PMDA. With language and subject expertise, our life science specialists ensure your regulatory documents meet local regulatory standards and are approval-ready.

Helping You Overcome All Challenges

Regulatory compliance is not just the key to acquire product licenses, but also the stepping-stone to access new markets. Ulatus’ localized regulatory submissions translation service builds the target language portfolio as explicit as the source language to gain a greater competitive advantage in the market. We manage the various regulatory documents with care and accuracy to protect your investments and ensure patient’s health. With an accurately localized content document, it becomes effortless to convey the essence of your product’s regulatory terms to the authoritative agencies. We overcome regional barriers and present the product’s information in a way that the authority understands and identifies with the text correctly. As also guaranteed, our regulatory submissions translation services delivers your message flawlessly and ensures compliance along with effective communication in the target market.

Some Of The Document-Types We Specialize In

  • Instructions for Uses (IFUs)
  • Package Information Leaflets (PILs)
  • Pharmaceutical Product Information
  • Summary of Product Characteristics (SmPC)
  • Chemistry, Manufacturing and Control Documentation (CMC)
  • Regulatory Dossiers
  • Packaging
  • Patient Prescribing Information
  • Standard Operating Procedures (SOPs)
  • Labeling
  • Common Technical Documents (CTDs)
  • Validation Documents
  • Regulatory Correspondence
  • Quality Review Documents (QRD)

Ulatus Advantage

When it comes to localization solutions, Ulatus provides the most efficient structures and equipment to guarantee maximum quality in any project!

Specialized Subject-Area Matching
Quality-Driven Technology
In-House Expertise
24x7 Dedicated Localization Manager
ROI-Driven Localization Solutions
ISO-Certified Processes

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