How do you check your translation quality?

We have a multi-layer QA system. Our system consists of QA team, software QA, multilayer translation assurance, random QA assessment, clinical review and more

Who performs the translation?

Our transltion is performed by specialize medical linguistic experts with a proven certification and experience in the matter field.

Can I revoke a translation or ask for amendments?

Yes, although its rare, we will support any amendments and discuss any issues with you, without any time limit. We follow up and support our clients around the clock and you can be sure your needs will be met.

How much does a translation cost?

There is no fixed price for a translation, as each client has different needs, every project, domain and language has its different properties. We will study your request and provide you with our best program and quote according to our local team's understandings.

Medical Translation / Pharmaceutical Translations

Pharmaceutical Translations

Processing Your Content

Around the globe Pharmaceutical translations are highly regulated translations that require special working protocols to be met, in order to deliver high-quality outcomes.

Special Requirments

Pharmaceutical translations require experienced and medically educated teams of linguistics experts. Besides that, specific training is required to comply with the strict requirements concerning terminology, layout, specific formatting, and specific software knowledge, which vary between different jurisdictions.

Compliance

Most pharmaceutical companies need to translate and localize many instruments to meet several regulatory requirements of entities, we are familiar with the various jurisdictions and local regulatory requirements and will help you focus on other sides of your clinical and regulatory duties.

Among the entities that we have long experience with are:

Food And Drug Administration (FDA).
European Medicines Agency (EMA).
Pharmaceutical and Food Safety Bureau (PFSB).
The Medicines and Healthcare products Regulatory Agency (MHRA).
Therapeutic Goods Administration (TGA).
Norwegian Medicines Agency (NoMA).
Food & Nutrition Services of the Israeli Ministry of Health.
The Ministry of Health (Minzdrav), Russia.
South African Health Products Regulatory Authority.
National Medical Products Administration (NMPA), China.
Central Drugs Standard Control Organization (CDSCO), India.

Furthermore, our experts deal with private ethnic communities and local nongovernmental regulatory entities, and international bodies to meet any specific requirements.

Let’s talk!