The Ministry of Economy, Trade and Industry (METI), jointly with the Financial Services Agency (FSA) and the Ministry of the Environment (MOE), has held repeated meetings of the Study Group for ...

Indian pharma’s global presence in generic medicine exports among others like biosimilars will indicate a strategic shift towards further expansion in the international markets particularly the US. To ...

Appropriate use of sound science applied at critical junctures will improve efficiency in the high-wire act of drug development. Pharmaceutical companies walk a tightrope in early drug development.

Accelerated formulation strategies are a useful tool to reduce development timelines and cost, but key priorities must be considered early on to ensure success. Although approximations vary ...

Expertise in CMC (chemistry, manufacturing, and control) ensures the appropriate manufacture of a pharmaceutical or biologic by coordinating material characterization, formulation development, and ...

The process usually takes between 14 and 18 months from publishing the final scope on the NICE website to approval of the final guidance by the NICE Guidance Executive (see chapter 10). The time taken ...

Nov 21 (Reuters) - U.S. Food and Drug Administration: * Says issued final guidance to assist the industry in their development of generic versions of approved abuse-deterrent formulation opioids‍ Sign ...

This is not the current manual. From January 2015, guidelines were developed using Developing NICE guidelines: the manual. The National Institute for Health and Clinical Excellence (NICE) is the ...