Clinical Development

Medical Writing

Translate complex scientific information into practical outputs with full regulatory compliance.

Comprehensive and Agile Medical Writing Services

We provide tailored and high-quality medical writing expertise across a broad range of therapeutic areas and document types, from IND application to clinical trial to post-marketing writing. With more than 20 years of experience partnering with pharmaceutical, biotech, and medical device clients, we offer protocol design and medical writing services in oncology, hematology, orthopedics, cardiovascular disease, respiratory, infectious disease, vaccine, etc., and dive into delivering high-quality solutions to meet full regulatory compliance.

  • In-house medical writers: 85% with M.S. degree, 20% with PhD. degree
  • Over 20 years of experience partnering with pharma, biotech and clinical site to provide customized medical writing solutions
  • A complete writing service spanning from individual documents to extensive writing programs, including: protocols, IND applications and NDA submission documents, informed consent forms, clinical development plan, clinical study reports, integrated summaries of safety and efficacy, etc.
  • Work closely with Biostatistics, Regulatory and Medical experts, and operational team to access a fully integrated network of information 
170+
IND applications for innovative drugs
41
Products served with NDA documents writing
29
Protocols of China-US Parallel Submission
13
Products served with MRCT documents writing

Medical Writing Capabilities across Full Clinical Development Lifecycle

We have professional writers in both China and US with knowledge of local regulations and a deep understanding of product features. With joint efforts of our clinical consulting teams and medical & pharmacology experts, we have delivered protocol designs for a number of Multi-region clinical trials (MRCT) and IND approvals in US and Australia.

始终与创新和勇气同行，永不止步

泰格医药企业宣传片

Why Tigermed for Medical Writing Solutions

In-house experts of SA, DM, regulatory, clinical pharmacology and clinical operation to manage and optimize document development to meet timelines

Industry-leading SOPs and in-depth therapeutic experience

Medical writing support spanning from individual documents to extensive medical writing programs.

Work closely with Biostatistics, Regulatory and Medical experts, and operational team to access a fully integrated network of information

Complete training system to ensure constant improvement of medical team

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