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03-06-2016
EMA: Accessing key information on human medicines

10-05-2016
NMMDA: New announcement for interested parties regarding medicines authorized based on studies performed within Semler Research Centre Private Ltd, Bangalore, India

04-05-2016
EMA: Meeting highlights from April 25-28, 2016 PRAC meeting

03-05-2016
NMMDA: Direct communication to Healthcare Professionals regarding medicines containing fusafungine

13-04-2016
EMA: CHMP meeting highlights

31-03-2016
EMA: Recommendations to minimize ketoacidosis risk with SGLT2 inhibitors for diabetes, confirmed

26-02-2016
NMMDA made am important announcement for interested parties regarding administration of anti-diabetes medicines

25-02-2016
The Ministry of Health issued a new order on approval of norms regarding authorization of wholesale distribution units of medicines of human use, good distribution practice certification and registration of human use medicines brokers

24-02-2016
EMA: Measures to help protect patients from falsified medicines

22-02-2016
NMMDA: Direct communication to healthcare professionals regarding Alexan (citarabina)

18-02-2016
NMMDA informs parties concerned with regard to Zika virus

03-02-2016
EMA: Meeting report on the development of a proactive approach to the prevention of medicines shortages due to manufacturing and quality issues

03-02-2016
EMA: Updated Guidance on the electronic submission of information on medicinal products for human use by marketing-authorization holders, issued

02-02-2016
Global pharmaceutical industry calls for collaboration with Governments

02-02-2016
NICE: New technology appraisal on different treatments for people with severe rheumatoid arthritis

02-02-2016
EMA: Splitting of the full presentation name of the medicinal product best practice

25-01-2016
EMA: Applications for new human medicines under evaluation by the Committee for Medicinal Products for Human Use

25-01-2016
Scientific Committee on Consumer Safety (SCCS) issues new revision of "Notes of Guidance"

20-01-2016
EGA adopts disclosure requirements for the generic, biosimilar and value added medicines industry

15-01-2016
New General chapter on High performance thin-layer chromatography of herbal drugs and herbal drug preparations endorsed

12-01-2016
EMA: Highlights from December 2015 meeting of the Committee for Advanced Therapies (CAT)

11-01-2016
EMA fast-trucks new oral treatment for non for non-small cell lung cancer for conditional approval

08-01-2016
Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP)

07-01-2016
Pharma industry announces financial agreement with the Department of Health

06-01-2016
The Bucharest Health Insurance House made a new announcement for all medical services, medicines and medical devices suppliers

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