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Tigermed’s medical department is composed of numerous highly qualified clinical experts and trained inspectors team, it has a sound quality management and quality control system to ensure compliance with ICH-GCP and the Chinese GCP requirements during the course of the project, and it can obtain high-quality clinical research data, to fully meet various needs of international and domestic clients for pharmaceutical products in clinical trial field. 

Tigermed have extensive clinical project management experience, good cooperation relationship with the hospital, and widely distributed offices. This not only ensures the process of the implementation of the project, but also shortens the duration of clinical trials, enabling new products into market at an earlier date.

Services Scope

Preparation of fundamental clinical trial documents (protocol, case report form (CRF), informed consent, etc.)

Clinical trial start-up (To choose principle investigator, clinical site, investigator meeting organization,

  ethics committee declaration, sign contract with the clinical site)

Clinical trial monitor
Clinical trial management
Clinical trial audit and quality control
Medical affair and pharmacovigilance

Clinical trial summary report writing


Providing medical advice of life cycle strategic plan to products
Writing and reviewing product promotional materials
Literature review of therapeutic field science and clinical research
Designing protocols and writing clinical summary report for Phase I, II, III, and post-marketing studies.
Preparing product training manuals, newsletters, conference highlights, patient health education and other services
IB and clinical development plan writing

Translation of scientific papers related to the product or other medical related articles


Experience in Medical Writing

Others includes rheumatology, psychiatric, stomatology, anesthesiology, surgical, medical devices, nutrition division, etc.