We translate Pharma-related Patents, Abstracts from Research Papers/Pharmacopeas, International Medical Journals and Magazines from all Foreign languages to English .
We translate Regulatory Affairs- related DMF (DRUG MASTER FILES) and SMF(SITE MASTER FILES) , Normative Documents for submitting at the Ministry of Public Health of Foreign countries for Registration.
We provide Technically and Professionally Qualified Experienced Interpreters for International GMP Audit Inspections conducted by Foreign Inspection Team at Indian and Foreign Pharma Plants.
We provide Interpreters for Out-station Pharma plants/companies (if required) if informed of the program in advance. In this case the company has to bear the total expenses like air-Ticket, accommodation, food and transportation including the Interpreters professional service charges.
Technical Interpreters of Language Translators of India have worked with the International GMP Audit Inspectors from SPAIN, GERMANY, FRANCE, JAPAN, RUSSIA, KAZAKHSTAN, UKRAINE, U.S. MEXICO at the Indian Pharma companies several times in the last several years and have satisfied both the Foreign Audit Inspectors and Local Company Representatives, Officers and Pharma Industry Experts.
A clinical trial being a critical process, it requires delivery of documents on time and with accuracy. LTI guarantees to provide desired clinical trial translations through its ISO quality processes that will also meet your budget and timeline. The translation experts for clinical trials have more than 25-30 years work experience in the medical field and are familiar with international regulations and standards. This translation service is explicitly available at every stage of the clinical trial and ensures that the documents are linguistically accurate and perfect for the targeted culture hosting the trial.
At LTI, we follow a clinical trial translation methodology which is tailor-made considering the regulatory requirements and constraints.
- Study Protocols
- Case Report Forms (CRFs)
- Case Study Reports
- Patient Diary/Event Log
- Patient-Reported Outcomes (PROs)
- Patient Records
- Informed Consent Forms (ICF)
- Patient Questionnaires
- Patient Consent Forms (PCF), Visit Diaries, Instructions list ( We translate from English to any Regional language)
- We can execute back translations of clinical trials- related documents(based on the requirement of the client using a different Translator and Editor.
- We issue Translation Quality Certificate along with the translated content
We would like to inform our most valued Customers that we at Language Translators of India maintain Secrecy and Confidentiality of all documents received from all our esteemed clients very strictly as per the legal guidelines existing in India. We are ready to sign any NDA/CDA with any company which offers huge translation assignments and based on long-term business activities .We take utmost care and security measures to maintain confidentiality of documents.
Because we give top priority to customer satisfaction and their growth in the competitive business world. We try to meet the clients requirements in all aspects.
We at Language Translators of India accept any volume of documentation in any Indian and Foreign languages for translation into English and vice versa. Language Translators of India is an Outstanding Translation Agency for executing Bulk Technical Translation Assignments from Foreign languages to English and vice versa.
Your translations are formally certified as a true translation and bear our firm stamp and signature. This can be used for official purposes and submission to government offices, consulates and embassies and other official authorities. Our document translation is subject to strict quality control processes to ensure the accuracy of your translation. Our translations are authentic as we are using only the services of certified translators and our translators refer authentic reference books and use appropriate words while translating into other language.