Medical Translation Service by Medical Translation Experts

Medical Translation

Pharmaceutical and medical translation requires expertise and accuracy, which can only be delivered by professionals who are highly specialized in healthcare industry. Accurately conveying the translated content is vital since the medical data contains innumerable complex terminologies. Certain disciplines within the translations are significant to the human life, and thus there is no room for error. Hence, an experienced medical translation services provider is a must for a complex industry like medicines. At Ulatus,we understand the sensitive nature of your medical work and ensure our security procedures are committed to attaining confidentiality and safety of your medical data.

Helping you overcome all challenges

Pharmaceutical, Medical Device and Healthcare industries rely on subject-matter experts for the most complex medical translations. These medical documents are exceptionally sensitive and may require to be updated several times in a year if instructed by the regulatory authority. At Ulatus, we have the experience and expertise to provide translations of the best professional standard. Our specialized team of linguists with scientific and medical backgrounds ensure the translations are in full compliance with applicable regulatory requirements. Moreover, our in-house technology ensures security of data while making sure all terminologies are accurate and the content is focused specifically on the target region.

A list of documents which we translate

✔  Medical Document Translation

✔  Regulatory Correspondence

✔  Patient Prescribing Information

✔  Healthcare Translation Services

✔  Fda Prescribing Information

✔  Pharmaceutical Translation Services

✔  Quality Review Documents (QRD)

✔  Common Technical Documents (CTDS)

✔  Instructions For Uses (IFUs)

✔  Summary Of Medical Product

✔  Medical Labeling

✔  Package Information Leaflets (PILs)

✔  Medical Validation Documents

Areas of expertise	Biochemistry, biostatistics, genetics, histopathology, pharmaceutical research
Highlights	- Japanese-Language Proficiency N1 Level Certification, 2010 - Contact Partnership Scholarship Recipient, University of California, Education Abroad Program - Awarded Dean’s Honor List
Years of experience	5+
Country	Japan
Education and Training	MD Rush Medical College, Chicago, Illinois, US BA Molecular and Cell Biology, Genetics and Development, University of California, California, US Medicine Resident, Fox Valley Family Medicine Residency Program, University of Wisconsin School of Medicine and Public Health, Appleton, US Graduate Diploma, Biochemistry, University of California Education Abroad Program, University of California, California, US
Work experience	Drug Safety Consultant, Brand Institute, Miami, Florida - Ensured that drugs met regulatory standards set forth by the FDA, the European Medicines Agency, Health Canada, and the Ministry of Health, Labour and Welfare in Japan. - Provided medication error prevention analysis associated with the labeling of pharmaceuticals, biological products, and medical devices. - Performed in-depth analysis of issues related to prescribing and dispensing, including consulting on all aspects of drug information, from profile to packaging to trade-dress. - Coded in Visual Basic, a screening tool that evaluates Katakana drug names for scripted similarities with existing drug names as per Japanese regulatory requirements. Bio-technician, Bayer HealthCare, Berkeley, California - Involved in managing constant perfusion fermentation and cell separation systems, operating and troubleshooting ultrafiltration technology and sampling for quality control Production Technologist, Bayer HealthCare, Berkeley, California - Played leadership roles in environmental safety, Six Sigma, and CIP (Continuous Improvement Process) projects

Areas of expertise	Cardiology, Cardiac/Cardiovascular Surgery, Molecular Biology, Hypertension, Anatomy, and Biology
Years of experience	10
Country	South Africa
Education and Training	Postgraduate Diploma in Public Health, Fiji School of Medicine, Suva, Fiji Certification, Capacity Enhancement Training of Health and Development, Japan International Cooperation Agency (JICA), Japan License of Medical Sonographer in Cardiology by the Japan Society of Ultrasonics in Medicine, Japan License of Clinical Laboratory Technician by Ministry of Health, Japan Training on Abdominal Ultrasound at National Cancer Center, Tokyo, Japan Bachelor of Economics, Saitama University, Saitama, Japan
Research and Publication	Contributed to “Compact Atlas of Echocardiography” (in Japanese) “Measurement Accuracy of Mitral Valve Area by Ultrasound Examination”, Japanese Journal of Medical Ultrasound Technology, in Japanese Wrote a thesis on “Characteristics of Social Figures and Economic Development in the Kingdom of Tonga”
Other Work Experience	Consultant of Japan’s ODA health projects and private hospital improvement projects Medical Sonographer and Clinical Laboratory Technician at hospitals in Japan Medical Sonographer at Hospital in Kingdom of Tonga Assistant of Biochemistry Laboratory of Medical University in Japan

Areas of expertise	Pharmaceutical research, Pharmaceutical chemistry, Pharmacotherapy, Cancer research, Food microbiology, Molecular biology, Histopathology, Nucleic acid research, Metabolism, General biochemistry, Dermatology, Cardiology, Endocrinology/Ophthalmology, Gastroenterology, Hepatology, Immunology, Infectious Diseases (HBV, HCV, HIV), Neurology, Oncology/Immuno-Oncology, Ophthalmology
Years of experience	10
Country	Brazil
Education and Training	Doctor of Pharmacy (Pharm.D.), Pharmacy and Biochemistry, Universidade de São Paulo, São Paulo, SP, Brazil Data Management for Clinical Research, Vanderbilt University, USA
Work experience	Clinical Data Quality Manager, Bristol-Myers Squibb Company, Brazil - Manage the data collected from 12 clinical trials distributed among 63 clinical sites in Brazil plus 6 clinical trials conducted in Canada. - Revision of quality metrics and data trends. - Performance of clinical listing review per Data Review Plan. - Site support on Serious Adverse Event reporting and follow-up. - Support sites with account registration for company’s systems. - Training/coaching on CRF/eCRF completion. - Data cleaning, eCRF application (coordination of Data Early Process Control and Ongoing Data Quality Control activities). - Provision of ongoing feedback on Oracle Clinical system validations/eCRF instructions and escalation of any data issues to upper managers. Clinical Research Associate, PPD do Brasil Suporte à Pesquisa Clínica / PPD Intl, Brazil - Phase II/III Diabetic Macular Edema (DME) trial - Phase I Anticonvulsant Therapy trial - Phase III Lupus Nephritis trial - Phase II Respiratory Syncytial Virus (RSV) trial Jr. Clinical Research Associate, AAIPharma/IPCSP, Brazil - Elaboration of clinical trial protocol, Informed Consent Forms (ICF) and Case Report Forms (CRF). - Translation of protocols, ICF, paper CRFs and trial-related manuals and contracts. - Electronic CRF training; certified e-CRF trainer Site Initiation Visits and Interim Monitoring Visits (IMV), monitoring reports, management and report of Serious Adverse Events, regulatory management, import and distribution of investigational products to sites, export of biological samples to central laboratories, clinical data management, organization and leadership of an Investigators’ Meeting. - Development and improvement of management tools for internal administration, monitoring visits and clinical trials. - Creation of electronic CRF, electronic monitoring forms, electronic SAE report form and electronic monitoring expenses report form (incorporated to the company’s portfolio and SOP). Translation Technical Manager, R A Serviços de Traduções Médicas e Científicas Ltda, Brazil - Translation of Clinical Trial Protocols, Investigator’s Brochures, Safety Reports, Regulatory Letters and Documents, Case Report Forms, Informed Consent Forms, Academic Articles. - Management, training and follow-up of a team of 192 translators. - Management of the company and assignment of duties to employees.

Areas of expertise	Homeopathy, Naturopathy, Nutritional-based Therapies, Health Information Management, Healthcare, Poli-cies/Economics, Hospital Management/Administration, Public Health Management/Administration, Allergology, History of Medicine, Pulmonology/Respiratory Medicine, Family Nursing, Geriatric Nursing, Home Health Nursing, Family Planning, Pharmaceutical Toxicology, Pharmacodynamics, Pharmacokinetics, Pharmacotherapy
Years of experience	30
Country	Taiwan
Education	Department of Pharmacy, Kaohsiung Medical University, Taiwan MBA, Texas State University, United States
Professional Training and Certification	Pharmacist certificate
Work experience	District sales manager of Pfizer Pharmaceutical Company Product manager, Schering-Plough Pharmaceutical Company OTC marketing manager, Sandoz Pharmaceutical Company Phamaceutical markeing manager, Novartis International AG
Research and Publication experience	Miller & Spoolman：Environmental Science 13/E
Skills	Chinese to English Translation