Medical Technology / Medical Devices

(65 results)(Back to Archives)

*In Vitro Diagnostics Technology and Industry Development Summit
Shanghai, China
18 Jun 2011 - 20 Jun 2010
Organized by eChinaChem, Inc., Shanghai Licensed Pharmacist Association, The Shanghai Medical Instrument Trade Association, Research Center of Econometrics, Shanghai Academy of Social Sciences, In Vitro Diagnostics Technology and Industry Development Summ.

*Virtual Webinar : Medical Device Process Validation
Palo Alto, United States
11 Mar 2011 - 11 Mar 2011
Attendees will receive a detailed understanding of process validation for medical devices approach employing IQ, OQ, and PQ.

*Conference On Indian Medical Devices & Plastics Disposables Industry 2011
Ahmedabad, India
11 Feb 2011 - 12 Feb 2011
With Special Focus on Medical Polymers and Processing, Device Manufacturing, Market Trends & Export Marketing, Regulations, Technology, Research & Market Developments, Packaging & Sterilization.

*Introduction to ISO 13485 Quality Management System for Medical Devices
Palo Alto, United States
21 Dec 2010 - 21 Dec 2010
This is an introductory course for section by section understanding of ISO 13485 requirements of a quality management system..

*CE Marking: Obtaining and Maintaining EU Compliance
Palo Alto, United States
14 Dec 2010 - 14 Dec 2010
This CE marking training will discuss the recent changes to MDD (Medical Device Directive), how to identify non compliance areas, contents of the technical file and essential requirements document and how to select notified bodies for MD compliance..

*BIT’s 3rd Annual World Congress of Regenerative Medicine & Stem Cells
Dalian, China
5 Dec 2010 - 7 Dec 2010
RMSC-2010 will be held at Shanghai Everbright Convention and Exhibition Center during December 5-7, 2010, with a theme of “From Bench to Bedside”, aim to move the Regenerative Medicine & Stem Cell research and development agenda forward..

*Medical Device Complaints Handling Strategies
Palo Alto, United States
2 Dec 2010 - 2 Dec 2010
This Medical device complaints handling webinar will discuss the best practices of complaint handling and how to include it in your CAPA program and how to apply risk management to the complaint handling system..

*Anatomy of a Medical Device Inspection: From EIR to 483 to Warning Letter
Palo Alto, United States
18 Nov 2010 - 18 Nov 2010
This Medical device inspection webinar training will teach you A to Z of inspection starting with how to prepare to what to do during inspection, close-out interview, FDA’s scope, what documents to show and how to respond to the inspection..

*How to reduce EO residuals in medical devices
Palo Alto, United States
18 Nov 2010 - 18 Nov 2010
This FDA Software Validation and Verification training/webinar will review the validation planning process with particular emphasis on avoiding six common pitfalls..

*The World Generic Medicines Congress Americas 2010
Washington, United States
16 Nov 2010 - 18 Nov 2010
The conference bridges the gap between international generic manufacturers, regulatory bodies, policy decision makers & financial organisations. It provides a forum focused on the key topics of the day, Make sure you are a part of this must attend meeting.

*Corrective and Preventive Actions(CAPA) - 8 Steps to Achieve Compliance
Palo Alto, United States
18 Nov 2010 - 18 Nov 2010
In this CAPA training webinar, we will focus on ideas that will help identify effective methods designed to improve your response to process deviations and help you develop a standardized plan to fully resolve discrepancies so they do not recur..

*Recalls of Medical Devices in the US
Palo Alto, United States
2 Nov 2010 - 2 Nov 2010
In this Medical device recall training learn how to interface with FDA in regards to anticipated recalls, the communication, the response, how to prepare the public information..

*Controlling Change to meet GMP Requirements
Palo Alto, United States
2 Nov 2010 - 2 Nov 2010
In this Medical device recall training learn how to interface with FDA in regards to anticipated recalls, the communication, the response, how to prepare the public information..

*Equipment Calibration, Maintenance, and Validation
Palo Alto, United States
9 Nov 2010 - 9 Nov 2010
This webinar will discuss the different aspects which auditors generally look in equipment calibration, maintenance and validation and highlight the best practices..

*Change Control Systems for Medical Devices
Palo Alto, United States
4 Nov 2010 - 4 Nov 2010
This change control training will discuss the best practices to create a FDA compliant system..

*An Easy to Implement Integrated Risk Management Approach Compliant with ISO 14971
Palo Alto, United States
29 Oct 2010 - 29 Oct 2010
This Integrated Risk Management Approach training in ISO 14971 will discuss how to incorporate risk management as per ISO 14971 in all phases of medical device development..

*Quality System Regulation (QSR) Management Responsibilities
Palo Alto, United States
28 Oct 2010 - 28 Oct 2010
This (QSR) Quality System Regulation webinar describes management responsibility by reviewing the Quality System Regulation (QSR) and the reasoning that FDA published..

*QSR Device Inspections – Transition from “Barely Surviving” to “Gaining Control”
Palo Alto, United States
27 Oct 2010 - 27 Oct 2010
This Medical Device Quality System training will discuss how to Create an adequate quality system that meets FDA’s requirements and Effectively prepare for upcoming Quality System Regulation (QSR) inspections..

*Gamma Sterilizer Validation: Method 1 and VDmax25 per ISO 11137
Palo Alto, United States
20 Oct 2010 - 20 Oct 2010
This Sterilization validation training will review the general requirements for validation as described in ISO 11137:2006..

*Key Considerations in Verification & Validation of Medical Devices
Palo Alto, United States
15 Oct 2010 - 15 Oct 2010
This Verification & Validation training for medical device will dissect some of the FDA 483 observations related to design verification and design validation and teach you how they can be prevented..

*The Exploratory Clinical Development World USA 2010
Cambridge, United States
19 Oct 2010 - 22 Oct 2010
The event is established as the leading strategic early clinical development event for pharmaceutical professionals. It targets the major challenges of the industry to find much needed solutions for best selection of drug candidates as early as possible..

*Project Management for FDA-Regulated Companies
Palo Alto, United States
5 Oct 2010 - 5 Oct 2010
This FDA-Regulated webinar on Project Management will discuss and provide examples of most common project management tools and how to use it immediately to comply with FDA and EU MDD regulations..

*Integrating Clinical Evaluation and Risk Management (ISO 14971)
Palo Alto, United States
7 Oct 2010 - 7 Oct 2010
This clinical evaluation & ISO 14971 training will discuss how the new changes in MDD and the risk management requirements per 14971 overlap and how manufacturers can establish one integrated system to meet both the requirements..

*Medical Moulding and Extrusion 2008
Cologne, Germany
16 Jun 2008 - 18 Jun 2008
The 2nd international conference on medical device manufacturing and materials from Applied Market Information Ltd. This event offers a forum for medical professionals specifying device requirements, medical device manufacturers and designers etc..

*ECM IX Fifty Years of AO: Internal Fixation: From Research to the Clinics.
Davos, Switzerland
15 Jun 2008 - 18 Jun 2008
4 day single session meeting, with free afternoons. Abstract deadlines Oral April 1st 2008, Poster May 1st 2008.

San Jose, CA, United States
3 Oct 2007 - 4 Oct 2007
The convergence of the medical device and biopharmaceutical industries has created a new rapidly growing industry sector; a wide range of biologic-device products are now the leading edge of medical device innovation..

*Bioengineering and Regenerative Medicine
Mulhouse, Alsace, France
24 Sep 2007 - 26 Sep 2007
The ambitious goal of this symposium, geographically located in the centre part of Europe, aspires to concentrate equally over 3 days researchers coming from various horizons and concerned with basic as well as clinical research..

*NanoEurope fair & conference
St. Gallen, Switzerland
11 Sep 2007 - 13 Sep 2007
In the past years, the NanoEurope has created a meeting platform as part of its fair and conferences in order to promote the exchange of knowledge and its commercialization..

*Medical Grade Polymers 2007
Philadelphia, PA, United States
12 Sep 2007 - 13 Sep 2007
The conference will provide an opportunity for the medical device industry to meet and discuss the latest developments in markets and technology..

Shanghai, China
28 Aug 2007 - 30 Aug 2007
This premier trade fair offered the opportunity to source everything needed to design and produce the full spectrum of advanced medical devices..

Plymouth, NH, United States
19 Aug 2007 - 24 Aug 2007
Mechanical Circulatory Support: Moving The Field Forward.

*BioDevice Partnering 2007
Zurich, Switzerland
12 Jun 2007 - 13 Jun 2007
A forum to promote interdisciplinary collaborations.

*In3 Medical Device Summit
San Francisco, CA, United States
3 Jun 2007 - 5 Jun 2007
The most important venue of its kind for previewing cutting-edge emerging medical technology companies and for engaging with the biggest dealmakers in the industry, including senior executives from the device industry and healthcare investment community,.

Sofia, Bulgaria
8 May 2007 - 11 May 2007
40 years the exhibition inevitably spreads its scales, serving the idea to help the thousands of physicians, dentists, laboratory assistants, pharmacists, rehabilitators, hospital managers, producers and distributors of medical and dental equipment etc..

Helliniko, Greece
15 Mar 2007 - 18 Mar 2007
Our Aim is to fully inform whoever is interested in this sector by creating an international exhibition which includes Technical and diagnostic equipment, technical therapeutic ICU equipment, laboratory and technical equipment, laboratory products etc..

*MDETEC 2007
Stuttgart, Germany
27 Feb 2007 - 3 Mar 2007
THE latest advances in medical-grade materials, components electronics, computer-aided design and manufacturing, production machinery, packaging, sterilization, quality systems, device communications, networking, enterprise IT…and much more..

*Medical Design & Manufacturing West
Anaheim, CA, United States
12 Feb 2007 - 15 Feb 2007
The total resource event for medical device and equipment manufacturers. Exposition 13-15 February; Conference 12-15 February.

*Post Market Surveillance & Vigilance for Medical Devices
London, United Kingdom
19 Feb 2007 - 22 Feb 2007
Medical device manufacturers must know what the current vigilance requirements and how to meet them in different countries throughout Europe..

*Medical Device Technology
Birmingham, United Kingdom
14 Feb 2007 - 15 Feb 2007
If you design or manufacture Medical Devices, then you need to attend MDT, the new MEDTEC event in 2007.

*American Academy of Orthopaedic Surgeons 2007 Annual Meeting
San Diego, CA, United States
14 Feb 2007 - 18 Feb 2007
Please join your colleagues and me in San Diego for the American Academy of Orthopaedic Surgeons’ 2007 Annual Meeting—the crossroads of orthopaedic education, research and technology..

*The UWEB Biomaterials Intensive Short Course
Seattle, Washington, United States
5 Feb 2007 - 7 Feb 2007
An Introduction to Biomaterials and Medical Device Applications.

*Photonics West 2007
San Jose, CA, United States
20 Jan 2007 - 25 Jan 2007
North America's largest commercial exhibition on optics, lasers, biomedical optics, optoelectronic components, & imaging technologies, Photonics West brings together more than 1,000 exhibitors, both local and international.

*BiOS 2007
San Jose, CA, United States
20 Jan 2007 - 21 Jan 2007
Biomedical Optics Weekend Exhibition.

*Failure Analysis Techniques
Farnborough, United Kingdom
25 Jan 2007 - 25 Jan 2007
The workshop is relevant to materials scientists and engineers, such as forensic engineers, independent consultants, QA engineers and students, who have not necessarily been trained in failure analysis, and who would benefit from general introductions to.

*Global Healthcare Conference " Promoting Partnerships"
New Dehli, India
15 Jan 2007 - 16 Jan 2007
Our endeavour is to bring together corporate leaders from healthcare and associated industries and policy makers, from India, UK, USA and South Asian Countries to deliberate on the emerging strategies, opportunities and challenges to define a road-map.

*Medifest '06
Delhi, India
22 Dec 2006 - 24 Dec 2006
The objective of this trade fair is to bring together all those related with the medical & healthcare sector, under one roof. The fair will provide the global overview and comprehensive information of the developments ..........

*Medical Device R&D Summit
Rancho Mirage, CA, United States
12 Nov 2006 - 14 Nov 2006
Will examine the extensive challenges affecting product development, benchmarking techniques for systems geared toward defining consumer necessities, thereby aiding in the development of successful device design..

*“BiomMedD’2006” and the 5th General Meeting of Romanian Society for Biomaterials
Iasi, Romania
9 Nov 2006 - 11 Nov 2006
This conference aims in bringing together the scientists and clinicians of various disciplines to discuss the present status of the biomaterials and medical devices, the achievements and the future perspectives..

*Biomedical Engineering Society Annual Meeting, BMES2006.
Chicago, Illinois, United States
11 Oct 2006 - 14 Oct 2006
BMES2006 will continue the tradition of offering excellent technical content and a meeting environment offering many opportunities for discussion and social interaction..

*3rd Annual Summit on Direct to Consumer Strategies for Medical Devices
Chicago, Illinois, United States
25 Sep 2006 - 26 Sep 2006
This conference provides medical device companies with methods to learn how to market their products directly to consumers while maneuvering within a very tight marketplace, with small budgets, high competition and a tremendous amount of people involved.

* The 8th IT Infrastructure Qualification Conference
Atlanta, GA, United States
25 Sep 2006 - 29 Sep 2006
This conference is designed for Pharmaceutical, Biotechnology, and Medical Device executives and staff.

*SBE's 2nd International Conference on Bioengineering and Nanotechnology
Santa Barbara, CA, United States
5 Sep 2006 - 7 Sep 2006
The Society for Biological Engineering (SBE) invites you to submit your abstract for our 2nd International Conference on Bioengineering & Nanotechnology (ICBN). Be a part of the conference that brings together leading researchers working at the interface.

*BioMech 2006
Palma de Mallorca, Spain
28 Aug 2006 - 30 Aug 2006
Fourth IASTED International Conference on BIOMECHANICS.

*3rd Annual Manufacturing Compliance for Medical Devices
Minneapolis, MN, United States
1 Aug 2006 - 3 Aug 2006
Key Topics: Understanding and Keeping Abreast of Regulations for Maintaining Compliance with Federal regulations, Embracing the International Arena: Knowing and Meeting the Demands of the Global Market, Guidelines and Labeling for Combination Products etc.

*Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
Irvine, CA, United States
7 Aug 2006 - 9 Aug 2006
This is a three-day course for people who must write within regulated environments. This course is valuable for pharmaceutical, medical device, and biotech professionals in drug discovery, product development, quality assurance, information technology etc.

*Drug|Device Summit 2006
San Diego, CA, United States
10 Jul 2006 - 12 Jul 2006
The Biotechnology Industry Organization (BIO) & BIOCOM, in partnership with Windhover Information, Inc. & Advanced Medical Technology Association (AdvaMed), will bring together the key stakeholders in biotechnology, pharmaceutical & medical device cos..

*European Society of Artificial Organs and tissue engineering Congress
Umea, Sweden
21 Jun 2006 - 24 Jun 2006
Abstract deadline Febr 28, max 250 words of all topics inthe field of artificial organs.

*2006 Summer Bioengineering Conference
Amelia Island, FL, United States
21 Jun 2006 - 25 Jun 2006
Some particular areas of highlight are stem cell bioengineering, nanobioengineering, biotherapeutics delivery, pediatric biofluid mechanics, and challenges in technology transfer..

*Advanced Summer Course in Cell-Materials Interactions 2006
Porto, Portugal
19 Jun 2006 - 23 Jun 2006
The course was designed for those who have an interest in the application of biomaterials, especially in cell-material interactions. This year it will focus on Regenerative Medicine..

*NanoBio 2006 - International Congress on Nanobiotechnology & Nanomedicine
San Fransisco, United States
19 Jun 2006 - 21 Jun 2006
Nanobiotechnology is a specialized field of nanotechnology, focusing on the improved and novel physical, chemical, and biological properties of materials at the nanoscale . Nanomedicine has potential impact on the prevention, early and reliable diagnosis.

*BioDevice Partnering - Building Convergent Medical Technologies
Edinburgh, United Kingdom
13 Jun 2006 - 14 Jun 2006
This new conferences series organized by EBD Group in partnership with Eucomed will focus on bringing together medical technology, biotech and biomaterial companies, exploring and fostering convergence in the healthcare sector..

*Canadian Medical and Biological Engineering Conference - 2006
Vancouver, Canada
1 Jun 2006 - 3 Jun 2006
The theme for CMBEC29 is: The Future of Medical Device Technology. Traditionally the CMBES has had 2 concurrent streams:Academic and Clinical Engineering..

*5th International Conference on Medical Polymers
Cologne, Germany
6 Jun 2006 - 7 Jun 2006
The conference will appeal to anyone associated with the medical device industry. It will be of particular value for businesses involved with design and manufacturing, raw material supply and compounding..

*Clinical Evaluations for Medical Devices
Brussels, Belgium
31 May 2006 - 1 Jun 2006
Changes and Challenges in the EU Regulatory Landscape..

*Medical Device Regulations
London, United Kingdom
24 May 2006 - 25 May 2006
A Practical Introductory Course on the Medical Device Directive for Medical Device Professionals, or professionals in regulatory affairs, product development and quality assurance, who are either newcomers to medical device regulation.

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