Pharmaceutical Manufacturers Translation Services

We make sure your pharmaceutical documents meet global rules with expert pharma translation. We offer FDA-compliant translation, GMP-compliant translation, and clinical and pharma translation for manufacturers.

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Why Choose Us for Pharma Translation Services

At Anan Translations our team focuses on pharmaceutical document translation and regulatory pharmaceutical translation to help manufacturers meet FDA, EMA, and CDSCO rules. We handle SmPC translation, Patient Information Leaflet (PIL) translation, and package insert translation.
We use ISO-certified processes for all work. Bilingual experts review it. We prepare it for global regulatory submission.

Medical Subject-Matter Experts

Native Linguists

On-Time Delivery

What We Translate

We cover all types of documents that pharmaceutical manufacturers need:

FDA-compliant translation
EMA document translation
CDSCO document translation
ICH guidelines translation
Drug regulatory submission translation

Batch record translation
Manufacturing SOP translation
CMC document translation
Stability study report translation

Clinical trial translation
Investigator brochure translation
Informed consent form translation
Pharmacovigilance translation
Medical device IFU translation

Pharmaceutical localization
Multilingual pharmaceutical translation
Pharma localization for global markets
Pharmaceutical export documentation translation
eCTD translation
Translation for pharmaceutical manufacturing companies
Pharma dossier translation for FDA submission

How We Work

Document Analysis & Terminology Mapping

Every pharmaceutical document translation starts with careful review for regulatory accuracy.

Domain-Specific Translation

Experts in clinical and pharma translation handle your documents using industry standards.

Bilingual Review & Quality Assurance

Checked by bilingual experts to maintain GMP compliance and regulatory adherence.

Final Validation for Regulatory Submission

Documents are ready for FDA, EMA, CDSCO, and other global authorities.

Industries We Serve

We work with a wide range of pharmaceutical and medical organizations:

Generic & Branded Drug Manufacturers

Biotech & Clinical Research Companies

Medical Device Companies

Contract Research Organizations (CROs)

FAQs

What types of documents can you handle for pharmaceutical translation?

We cover regulatory, manufacturing, clinical, and marketing documents, including batch records, SOPs, SmPC, PILs, package inserts, and eCTD submissions.

Are your translations FDA and GMP compliant?

Can you handle multilingual pharmaceutical translation for global markets?