PHARMA JAPAN welcomes JETRO New York’s Shunsuke Tani as a guest columnist. In occasional contributions, Tani will share his perspectives on US pharmaceutical policy, industry developments, and life in America, drawing on his firsthand experience in the US.---Hello from New…
REGULATORY
JPMA Official Calls for Partial Introduction of CDISC-Based Electronic Applications; Runup Period too Short
Masaaki Kuwahara (Senior Director, Regulatory Affairs Department, Development Center Japan, Pharmaceutical Development Division, Takeda Pharmaceutical), chairman of the Japan Pharmaceutical Manufacturers Association’s (JPMA) Regulatory Affairs Committee, spoke on the electronic applications that will become mandatory from FY2016 at a symposium…
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REGULATORY
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