Who we are

iso9001_2008 Williams Language Solutions provides Translation, Editing and Proof-reading (TEP) of written documentation including Patents.

Originally founded by Stefania De Angelis Williams to provide English into Italian translations, Williams Language Solutions is proud to have developed strategic alliances with freelance translators, consultants, editing and design companies in Europe and the US, to provide the clients with high quality translation and editing services in most European languages. Stefania still actively works as an English into Italian translator working directly with many clients and agencies (working effectively as a “freelance translator” in this case), and also coordinates multilingual projects. She is usually the first point of contacts for the clients.

The company is best described as a network of professional translators proactively working to ensure clear and correct transfer of information from one language to another.
The latest ICT solutions are employed to increase performance, speed up work and nurture business contacts.

Translators

Most of our translators and editors hold an advanced degree in science and/or medicine (Ph.D., degree or M.D.), and some of them have also extensive publication records. They are selected from the main linguists associations recognised in the UK and worldwide, and all adhere to a code of conduct of confidentiality on documents and clients. We translate many types of medical and pharmaceuticals documents, specifically IVD, antibodies, probes, detection systems, histology, IHC, ISH, PCR, patents, clinical trials, PIS.

Most of our translators and editors hold an advanced degree in science and/or medicine (Ph.D., degree or M.D.), and some of them have also extensive publication records. They are selected from the main linguists associations recognised in the UK and worldwide, and all adhere to a code of conduct of confidentiality on documents and clients. We translate many types of medical and pharmaceuticals documents, specifically IVD, antibodies, probes, detection systems, histology, IHC, ISH, PCR, patents, clinical trials, PIS.

Quality control

Our Quality Control procedures start long before the project, through the careful selection of the translators to be assigned to each text. Depending on the request of the client and the destination of use of the document, a translation undergoes a 2- or 3-stage process (translation, validation, expert editing), and clients are constantly updated on the progress of their translations by logging on a dedicated area on the bespoke XTRF translation management software; the contact with the Project Manager is ongoing during the project and continues after the delivery, during the feedback and evaluation stage. This will provide our clients with the confidence of knowing that we comply in all respects with the highest quality standards in the translation industry.

The company makes extensive use of a third party software package called XTRFTM which has been specifically designed to manage all aspects of translation services in accordance with BS EN 15038 and incorporating ISO 9001 related elements.

Most of our translators and editors hold an advanced degree in science and/or medicine (Ph.D., degree or M.D.), and some of them have also extensive publication records. They are selected from the main linguists associations recognised in the UK and worldwide, and all adhere to a code of conduct of confidentiality on documents and clients. We translate many types of medical and pharmaceuticals documents, specifically IVD, antibodies, probes, detection systems, histology, IHC, ISH, PCR, patents, clinical trials, PIS.