HOME > Services > Support for development of pharmaceuticals > Medical writing

Services

Medical writing

MIC provides all necessary support for reports required in all steps towards approval of products, including notification of a clinical study, reporting of adverse reactions, and preparation of clinical study report. Experts with long-term experience provide such services.

1．Support for preparation of documents regarding notification of a clinical trial
(1)Notification of a clinical trial (draft) in compliance with SGML
(2)Protocol (draft)
(3)Informed Consent Form (draft)
(4)Case Report Form (draft)
(5) Investigator's Brochure (draft)

2．Support for preparation of reports on adverse reactions regarding investigational product

3．Support for preparation of clinical report

4．Support for preparation of summary of approval application

（Inquiry / Request for Brochure）
MIC Medical Corp.
Yushima Urban Bldg, 2-31-22 Yushima, Bunkyo-ku,Tokyo 113-0034 Japan
Business development Dept.
Hidenori Numata
Tel: +81-3-3818-8580 Fax：+81-3-3818-8570
Inquiry
（Please make sure to mention your COMPANY NAME, ADDRESS, and TELEPHONE NUMBER in the inquiry form)

Direct Regulatory Affairs Dept.
Kenichi Sakamoto
Tel: +81-3-3818-8201 Fax：+81-3-3818-8570
Inquiry
（Please make sure to mention your COMPANY NAME, ADDRESS, and TELEPHONE NUMBER in the inquiry form)