Die Produktexperten von BSI sprechen auf Veranstaltungen und Konferenzen

Als eine der weltweit führenden Organisationen, die sich dem Anheben der Standards verschrieben haben, sprechen unsere Produktexperten auf Branchenkonferenzen und Veranstaltungen auf der ganzen Welt.

Wir bringen unsere Erfahrung und unser Know-how zu zentralen Themen zusammen, die Ihr Business beeinflussen, wie Gesetzgebung, Risiken und Schlüsselfaktoren für die Implementierung. Nachstehend finden Sie eine aktuelle Liste von Konferenzen und Veranstaltungen, bei denen Referenten von BSI sprechen.

The latest events that we are speaking at include:

For events that we attend only these are highlighted in the 'Speaker' column.

2014 Events

October events

Date

Speaker

Event

Details

16 Oct

Stefan Burde

AMDM Focus Meeting

USA - EU IVD Regulatory Update, Association of Medical Diagnostics Manufacturers.

20 Oct

Gert Bos

7th Annual European Medical Device Clinical Research

Germany - The upcoming medical device regulation and expected impact on clinical operations MDR impact on notified body role and scrutiny. Q1 Productions.

27 Oct

Stefan Burde

5th Annual Clinical Affairs and Regulatory Approvals for Diagnostics Conference

USA - Preparing for changing IVD Medical Device Directives in Europe, Q1 Productions.

28 Oct

Amie Smirthwaite

Imperial College event

UK - CE marking, Imperial College.


November events

Date

Speaker

Event

Details

03 Nov

Paul Brooks

Annual Medical Device Clearance & Approval Conference

USA - EU Regulatory Update, Q1 Productions.

05 Nov

Paul Brooks

FDA/UGA Medical Device Conference

USA - EU Regulatory Update, University of Georgia / FDA.

05 Nov

Paul Sim

PTI Informa Medical Device School

UK - Operating in a Quality Management System, PTI Informa.

17 Nov

Suzanne Haliday

Functionally Stratified Design and Manufacture of Orthopaedic Devices 

UK - EU Regulatory Update, MeDe Innovation.

19 Nov

Sophie Tabutin & Bianca Lutters

9th annual Drug Device Combination Products conference

Germany - Extended evening discussion: Gaining key insight on the rationale behind the classification of combination products, borderline products and new technologies, Informa Life Sciences.

20 Nov

Sophie Tabutin

9th annual Drug Device Combination Products conference

Germany - Interactive session: Notified Body panel: Evaluating the processes and findings of unannounced manufacturer audits and testing by Notified Bodies, Informa Life Sciences.

20 Nov

Bianca Lutters

9th annual Drug Device Combination Products conference

Germany - Examining the results and implications of joint Competent Authority audits and the formation of Team NB, Informa Life Sciences.

20 Nov

Paul Sim

Quality Management Systems for Medical devices

UK - Quality Management Systems for Medical devices, Management Forum.

25 Nov

Neil Adams

ABHI Annual Regulatory Conference: From Directives to a Single Regulation

UK - How key elements in the MDR will affect you, Notified Body perspective, ABHI.

25 Nov

Ann Goodall

In-Vitro Diagnostics Directive (IVDD)

UK - IVDD Gain a comprehensive understanding of the regulation, Management Forum.


December events

Date

Speaker

Event

Details

02 Dec

Sue Spencer

IVD Regulatory and Strategic Forum

UK - Preparing for new Notified Body responsibilities and challenges under the new IVD regulation Informa.

03 Dec

Amie Smirthwaite

Biocompatibility Testing and Evaluations for Medical Device

Germany - Notified Body perspective: Practical advice on successful biocompatibility submissions, Informa.

08 Dec

Gert Bos

3rd Annual European Quality Assurance in Device and Diagnostic Manufacturing

Germany - Examining how the MDR & IVDR are shaping the new Notified Body role in Europe, Q1 Productions.

09 Dec

Neil Adams

Genesis 2014 Conference

UK - Gathering the right evidence for the right outcome. Is Medical Device and IVD Regulation moving in the Pharma direction? One Nucleus?

10 Dec

Yoko Sawada

Institute of Industrial Promotion Kawasaki Seminar

Japan - Impact of JPAL update to SMEs, Institute of Industrial Promotion Kawasaki.


2015 Events

January events

Date

Speaker

Event

Details

27 Jan

Gert Bos

Informa's The European Medical Device Regulation

Belgium - Understanding the impact of joint audits of Notified Bodies (by Member States and the European Commission) on industry, Informa.


February events

Date

Speaker

Event

Details

17 Feb

Gert Bos

Clinical Operations and Outsourcing in Medical Device Trials conference

Germany - Investigating the changing regulatory landscape for medical devices disclosing expectations from regulatory bodies, Arena.


April events

Date

Speaker

Event

Details

14 Apr

Neil Adams

DIA European Meeting 2015

France - New Medical Device Regulations in the EU, DIA.

21 Apr

Paul Sim

MEDTEC Europe 2015

Germany - TBC, UDM Canon.