2013 Enews

2013 Enews

22 November 2013

A Double-Dose of Medicine for BSI >

BSI is delighted to update you on a significant investment and expansion of our in-house medicinal expertise.

12 November 2013

Medical Device Single Audit Program (MDSAP) >

BSI would like to draw your attention to the MDSAP Pilot Program that is starting in 2014, that will have significant impact on your Medical Device Audits in the future. Read more.

BSI's approach to reviewing electronic IFUs >

Read more.

27 March 2013

Regulation EU (No) 722/2012 – New Regulation regarding medical devices utilizing tissues of animal origin >

European Union Commission Regulation No 722/2012 concerning both active implantable medical devices (AIMD) and medical devices manufactured utilizing tissues of animal origin was originally published in the Official Journal of the European Union on 9th August 2012.Read more.

22 October 2013

European Parliament votes on Pre Market Authorization (PMA) elements in high risk device market access >

Today, (22 October 2013) the European Parliament made a decision in the first Reading on the future of medical device regulations in Europe. Read more.

25 September 2013

From California to Boston BSI takes its product experts on the road >

Another successful 2013 medical devices roadshow for BSI in America during September. Read more.

08 June 2013

Unannounced audits for manufacturers with CE certification >

Unannounced audits are coming, and will not be optional for Notified Bodies to perform or for manufacturers to receive. Read more.

29 July 2013

Malaysian Medical Devices Authority appoints BSI as a Conformity Assessment Body for Medical Devices Act 2012 >

BSI now registered as a Conformity Assessment Body (CAB). Read more.

24 May 2013

BSI Medical Devices hosts it's first successful forum in Shanghai >

BSI China supported by the Global Medical Device team held their first Medical Device Forum in Shanghai. Read more.

05 February 2013

EN ISO 14971:2012 - what does it mean for Manufacturers placing products on the European Market? >

EN ISO 14971:2012 - what does it mean for Manufacturers placing products on the European Market?

19 February 2013

Guide to European Medical Device Trials and BS EN ISO 14155 >

Get your copy of the new ‘go to’ guide for medical device trials. Read more.

02 May 2013

Interested in supplying your medical devices in the Kingdom of Saudi Arabia? >

Learn about the SFDA Market Authorisation. Read more.

24 January 2013

European Medical Device Expert Group Meeting Update >

Read about the first MDEG meeting of 2013 held in Brussels. Read more.

22 January 2013

Changes to the European / Australian Mutual Recognition Agreement (MRA) >

The Australian TGA and European Commission have announced changes in the EU / Australia MRA taking effect January 1, 2013. Read more.