Life Sciences Translations
High-quality life sciences translation services by industry experts
As a professional in the life sciences industry, you know that the documentation pertaining to your product development and testing process must be accurate and complete. The same is true for product usage instructions and sales and marketing communications that are critical to your product launch efforts. In both cases, translation is an integral part of the process.
- Overview
Find out more about Merrill Brink.
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Merrill Brink is ISO-certified
Merrill Brink International is an ISO-certified expert provider of high-quality scientific and technical translations for the pharmaceutical, medical device, diagnostics, biotechnology and clinical research companies. We understand the precision, adherence to deadlines and risk management requirements of the life sciences industry and can ensure that your product and marketing information is technically precise, while also culturally sensitive and relevant.
Merrill Brink has over 30 years of experience in the life sciences industry
Our linguists’ subject matter expertise and linguistic harmonization skills are second to none. This expertise ensures accuracy and consistency in terminology, adherence to local market idioms and reduces the risk of errors and the need for time-consuming edits.
Our project managers are highly trained and committed so you can delegate with complete confidence, knowing that our team will deliver high-quality results, on time and on budget.
We provide high-quality translation services in disciplines such as:
- Audiology
- Biotechnology
- Cardiology
- Diagnostics
- Endoscopy
- Gynecology
- Neurology
- Orthopedics
- Pharmacology
- Urology
- Vascular
Additionally, Merrill Brink has proven experience with the following regulatory and risk management standards:
- Compliance with the European Union Directives
- Medical Device Directive 93/42/EEC (MDD)
- In Vitro Diagnostic Medical Device Directive 98/79/EEC (IVDD)
- Active Implantable Medical Device Directive 90/385/EEC (AIMDD)
- Directive 2004/27/EC concerning human medicines
- Risk management for labeling and documentation
- Translation services for CE Mark requirements