Pharmatutor

JULY 18, 2022

This has also resulted into stricter norms for Marketing Authorization (MA) and Good Manufacturing Practices (GMPs). Mon, 07/18/2022 - 15:31. Read more about Drug Regulatory Affairs Certificate Institutes in India Log in or register to post comments

Safety 59

Safety Manufacturing Pharmaceutical Marketing 59

Pharmaceutical Technology

JULY 14, 2022

Due to the high price tags associated with these speciality medicines, innovators have naturally favoured big markets with high GDP such as the US and EU-5 (Germany, France, Spain, Italy, and the UK). “The Go-to-market strategies. The choice of where to launch an orphan drug is an important and difficult decision.

Medicine 59

Medicine Marketing Specialization Pharma 59

pharmaphorum

SEPTEMBER 30, 2022

The process starts adding fields to regulatory submission templates that will incorporate re-used information, then building templates with standardized structures and including structured data tags and sources. Fillable metadata is next added to the templates. He is a strong proponent of standards and data governance.

Management 52

Management Pharmaceutical Marketing Electronics 52

Evolve Your Success

JUNE 13, 2023

Click To Tweet I always try to leave myself with a good contact in the office, whether it’s an MA, an office manager, or somebody I can almost be on a texting level with where I don’t have to call, be on hold, and go through, “Click three for this person.” I’ll walk your MA through how to do it.” They just want the name tag.

Sales 52

Sales Medical sales Medical Doctors 52