Ind AS 115 – Key impact for life sciences entities
Jalpa Sonchhatra, Director, Financial Accounting Advisory Services, EY India speaks on the strategies needed to ensure compliance…
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Fix DAVA portal, says industry to DGFT
Faced with delays at ports and possible product recalls, industry hopes the DGFT will fix the issues with the DAVA portal as well…
Opportunity for biotech firms to pursue drug candidates targeting metabolic disorders
The GlobalData report found that big pharma companies lag behind small bio-techs in R&D efforts
E-pharmacies in India — Regulatory landscape and challenges
Sarthak Sarin (Principal Associate) and Bharat Gupta (Associate), Khaitan & Co, give an insight on the need for better…
Number of IO trials in China surge by more than 50 per cent in 2016 and 2017
GlobalData identified 819 clinical trials that have been initiated in the last 10 years (2008-17) to investigate I/O drug…
Digital technologies are definitely important in ensuring compliance with GMP standards
Pharma companies these days have to comply with a number of standards as governed by Good Manufacturing Practice (GMP) and FDA…
Legal framework of PV for medicines marketed in India
Rajdutt Shekhar Singh, Partner, Singh & Associates, gives an insight on the status and objective of pharmacovigilance…
Driving change at Novo Nordisk
As Novo Nordisk implements a change strategy to expands its focus from diabetes to other chronic conditions like obesity, it is…
Selling in the new age
In the first of a new series of articles, Mohan G Joshi, international business coach and speaker on sales and leadership,…