Clinical Development

Medical Writing

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

High-quality 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 17 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.

  • Phase I-IV drug and medical device protocols
  • Clinical study reports (Phase I-IV): patient narratives /appendices /publishing /basic results disclosure /lay summaries /redaction
  • Informed consent forms
  • Clinical development plan
  • Investigator brochures
  • Clinical overview (module 2.5), Clinical summaries (module 2.7), Integrated summaries of safety and efficacy, RMP.
  • Investigator meeting materials

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.

1,640+
Medical writing projects
75
Innovative drug IND protocols
15
Therapeutic areas for NDA dossiers

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

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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. 

30+ highly skilled and experienced writers with medical background

Complete training system to ensure constant improvement of medical team

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