Pharmaceutical Clinical trial &
Medical Devices Document Translation Service

Clinical Trials

Many pharmaceutical companies face difficulty in finding a specialized translation company. Ultimately, entrusting translation tasks to unqualified translators or handling them within the company's departments results in a decrease in operational efficiency.

By outsourcing translation to medical field experts, you can save time and costs, maximize operational efficiency, and enhance your company's competitiveness. Encopharm is Asia's leading medical field specialized translation company, primarily composed of pharmacists with extensive experience in the industry. Our team at Encopharm consists of expert translators familiar with research experiments and clinical trial terminology. Our clinical dedicated translation team provides accurate and consistent translations in all languages through a professional and systematic approach.

The services offered by Encopharm include:

Clinical trial brochures, clinical trial protocols, packaging labels, product packaging instructions, participant information sheets, informed consent forms, preclinical monitoring reports, medical/laboratory/technical procedure manuals/tests, clinical trial monitoring reports based on clinical trial participant requests for clarity, adverse reaction reports, questionnaires, participant selection records, the latest information on medical/laboratory/technical procedure manuals/tests, substantial changes to the clinical trial protocol, other document information for participant submission, final clinical trial completion monitoring reports, treatment group allocation and unblinding documents, final reports for clinical trial participants as requested by the Ethics Committee, and clinical trial result reports.
Encopharm takes pride in providing high-quality services to customers in the rapidly specializing pharmaceutical market, contributing to the development of our customers.

Medical Device

Due to the rapid globalization of the pharmaceutical market, delivering product information promptly in local languages is the top priority for manufacturers. To supply medical devices promptly, information about products and services in local languages is needed at the right time, especially to facilitate smooth regulatory approval locally. Encopharm offers services to support customers in entering overseas markets quickly and efficiently, including:

• Providing services where all information from a company is translated into multiple relevant languages.
• Writing and providing methods for product labels and related documents that comply with local legal requirements.
• Providing accurate information about the local market.

Encopharm professionally handles extensive and complex document tasks in various media that your company may need. We assist your brand in saving time and costs, ensuring successful progress in the international market.



Global ENCO-Pharm CRO Consulting

ENCO-Pharm CRO Services

Preclinical CRO Premium Consulting

- Offering services such as compound synthesis, compound activity screening, structural biology, CMC, pharmacology evaluation, pharmacokinetics, and toxicological safety assessment.

Regulatory Approval (FDA, NMPA)

We provide in-depth services for NMPA (National Medical Products Administration) and U.S. FDA (Food and Drug Administration) IND/ANDA applications for both domestic and international clients based on a profound understanding of the regulatory environments and pharmaceutical application requirements in China and the United States."

• We offer one-stop research, comprehensive project management, and submission services in collaboration with a specialized IND and ANDA research team.
• Our rich resources, composed of NMPA and FDA review experts, provide tailored advice on technology, regulations, and application strategies.
• The Global ENCO-Pharm's IND submission service platform offers customers customized registration strategies, prevents potential registration risks, ensures timely and accurate document submissions, and supports customers in completing the registration review process quickly by tracking the progress of the review.

Global ENCO-Pharm CRO Consulting is prepared as follows to provide you with prompt and efficient support for clinical trials:

• Fast regulatory approval! Cost savings in new drug development! Shortened timelines!
• Customized CRO services through the global pharmaceutical and clinical networks of Global HarrisCo and ENCO-Pharm.
• Providing rapid research outcomes with minimal drug development costs.