Medical Device Seminar Bringing your medical products to United States of America (USA)

Similar documents
Workshop on Design for Compliance to IEC (3rd Edition) and EMC Standards & Requirements. 14 th - 15 th May 2015 TÜV SÜD

In-Vitro Diagnostic Directive (IVDD) and IVDD Technical File Preparation Workshop. 3-4 July 2014 TÜV SÜD

EMC & RF Workshop. 9 th November 2017 TÜV SÜD

Seminar on Revision of ISO 9001:2015 & ISO14001:2015 Standards

Industrial Automation and Robotics

Automotive Testing & Certification Seminar. 21 February 2014 TÜV SÜD PSB

Achieving Sustainability through Green Building

Green Building/LEED AP Building Design & Construction Exam Preparation

ISO 55001: 2014 Asset Management System 5-Day Training Course (IAM Certified)

Certified Building Commissioning Professional (CBCP )

ISPE THAILAND AND TIPA 2017

In-House Microbial Isolates in Compendial Testing: Regulatory Requirements

Global Impact for a Safe and Sustainable Future

The forum will cover the key legislative amendments in the Companies (Amendment) Act 2014 and the practical applications and key filing requirements.

RISK BASED INTERNAL AUDIT (16 CPE) COSO ERM Framework - Risk Assessment Process

Static Charge: The Invisible Contaminant

Workshop description

What Disinfectants Do You Need - FDA or EPA Registered

Master the implementation and management of a Cybersecurity Program based on ISO/IEC 27032

Radware. Training Policies V001.70

Rapid Microbiological Techniques - Applications, Strategies, and Regulatory Expectations

Operations & Technology Seminar. Tuesday, November 8, 2016 Crowne Plaza Monroe, Monroe Township, NJ

GMP/GDP auditor training course

Non-Viable Particle Monitoring of Cleanrooms - Periodic and Continuous Monitoring

Personnel Certification

Advanced Systems, Inc. Course. Registration Form. (Please complete all information)

MAY. (Tue) Hong Kong. CYBERSECURITY & RISK MANAGEMENT How to preempt cybersecurity challenges in the digital world

raining Meeting your training needs and CPE requirements opportunities July-September Group-Live Course Group Internet- Based Course

Environmental Monitoring Program for Medical Devices per Current Guidances New AAMI and ISO EM Reference Documents and Standards

Training Opportunities

IT Audit Essentials. Date: 10 th 12 th March 2015 Time: 9 am to 5.30 pm Venue: Iverson Associates, Center Point Bandar Utama, Kuala Lumpur

COBIT 5 Foundation Workshop

Danfoss Turbocor Learning Center

ACCA Diploma in. Starting this January! International Financial Reporting (DipIFR)

Sample Site Selection Locations for RABS and Isolators

MANAGER OF LANDFILL OPERATIONS (MOLO) 3-Day Certification Course

Certified Compliance Professional (CCP) TM

SAVE THE DATE MARCH Basics of St. Charles, MO CLICK HERE to register online!

New Horizons in Audit & Assurance

Supporting Organization: Sponsorship:

Advances in Well Testing and Wireline Formation Testing

Global Impact for a Safe and Sustainable Future

The Institute of Internal Auditors San Gabriel Valley Chapter

MEMBERS CIRCULAR 13 June 2016 Ref 0028/06/16

ACIIA CAE Leadership Forum. Collaboration Innovation and Duplication: Making Great Things Happen

ACCA DipIFR. Diploma in. International Financial Reporting

October 21-23, 2013 Holly Springs, NC

Professional Evaluation and Certification Board Frequently Asked Questions

Antimicrobial Effectiveness Testing - Understanding the Basics

MY PUBLIC ACCOUNTANT PRACTICE PROGRAM Preparation for practice success

raining Meeting your training needs and CPE requirements opportunities July-September Group-Live Course Group Internet- Based Course

TEST REPORT: CHM17-YL-01

FACTS FIGURES TÜV SÜD AG

2018 Practice Education Course Registration Form

BASED INTERNAL AUDITING

The course fee for Provident & Tax for CPF Subscribers Training (1 Day) is $ (inclusive GST)

ECF on Anti-Money Laundering and Counter-Financing of Terrorism (AML/CFT) Frequently Asked Questions

Managing Risk through GFSI

THE 2017 REGULATORY SUMMIT

CFSE / CFSP Training & Certification

2018 Government Professional Accounting Seminar

Become a Certified Association Executive through the CAE Program

NC SWANA Managers Training Center

BCS London Office Southampton Street, London, WC1.

Featuring California-Specific SWANA MOLO Training In Today s World, You Can t Afford NOT To Be Trained & Certified

16TH ANNUAL HEALTHCARE SUMMIT

G7 Expert Certification (Sheetfed Offset Printing) (Location: Hong Kong)

CDCS Recertification Handbook 2014

Cleanroom Microbiology for Non-Microbiologists

ATTENDEE REGISTRATION POLICY

Configuration, Installation, Commissioning, Troubleshooting, Operation & Maintenance

DELEGATE INFORMATION PACK 2019

Partnership Information

raining Meeting your training needs and CPE requirements opportunities April-June Group-Live Course Group Internet- Based Course

Advanced Systems, Inc. Registration Form. (Please complete all information)

CYBER FRAUD & DATA BREACHES 16 CPE s May 16-17, 2018

Information Security Officer (ISO) Education

Investigating Microbial Data Deviations

EXAMINATION ENTRY REGISTRATION (NOVEMBER 2014)

A MASTER CLASS AUDIT, LEADERSHIP & ADVANCED EXCEL WORKSHOP

1 st Annual Meeting for Abacus Latin America Members

Client Services Procedure Manual

Certified Building Commissioning Professional (CBCP )

Danfoss Turbocor Learning Center

FUNDAMENTALS OF SUBSTATIONS FOR NON-ENGINEERS

Excel VBA for Absolute Beginners

DNA Certification Programs Overview (as of 10 June 2006)

Information and Rules for Candidates taking IFE Examinations in March 2019

Certification in ISO (3 day masterclasses)

Damage Prevention Symposium

MEMBERS CIRCULAR 12 February 2015 Ref 003/02/15

Governmental Workshop

MANAGING PROJECTS USING PMI S STANDARDS. Facilitated by Mr. Andreas Solomou. 12, 19, 26 November and 3, 10 December :30 17:00

Information Security Workshop

INFORMATION TECHNOLOGY AUDIT &

PROFIBUS TRAINING COURSE REGISTRATION FORMS

AVIATION CYBER SECURITY TRAINING

Please indicate the branch of engineering/discipline to be placed on the register of Chartered Engineers of Singapore:

-- Smart Grid Communication --

October 9-11, 2012 Lenexa, KS

Transcription:

Medical Device Seminar Bringing your medical products to United States of America (USA) 4 th June 2015 TÜV SÜD

Introduction Healthcare improvements rely on an innovative and diverse medical device sector around the world. But as the market grows, so too does the regulatory environment and the pressure on timelines. To guarantee swift market access, manufacturers must respond quickly and effectively to regulatory changes as they happen. They need to ensure that their products meet expectations of quality, safety and performance prior to launch in order to achieve quick, cost-efficient market acceptance. This seminar is specially organized for medical technology companies seeking entry to United States. At an estimated US$125.4 billion in 2013, the US medical device market is the world's largest. Per capita expenditure, at US$392, is the second highest in the world, behind only Switzerland. In addition, the medical device imports increased by 4.6% to reach a record high of US$37,751 million in 2013. The running annual total reached US$38.9 billion in the 12 months to August 2014, representing y-o-y growth of 5.1%. With the facts speaking for itself, the USA is the most attractive market in the world, particularly for commercializing a medical device (Source: BMI's Medical Device Risk/Reward Ratings (RRRs)). However, there is a challenge common to all medical device manufacturers. Due to the nature of the products to be used in healthcare, the market is very much regulated to ensure that patients have access to high quality, safe and effective medical devices. As such, this seminar aims to address this challenge by providing the local medical technology companies with good knowledge and understanding of what it takes to sell a medical device in the US market. 02

Who Should Attend This seminar is designed for a multidisciplinary audience of: Medical Device Business Owners Medical Device Companies CEOs Managing Directors and Directors Regulatory Affairs Directors/ Managers / Specialists Quality Assurance Directors/ Managers / Specialists Product Managers / Engineers and Medical Device Consultants About the Speaker Vice President Quality & Regulatory Affairs TÜV SÜD America Inc. Mr. Gary Minks is currently the Vice President of Quality & Regulatory Affairs for TÜV SÜD America Inc., overseeing all certification programs for both management systems and product certifications. He first joined TÜV SÜD more than 22 years ago as a Quality Systems Lead Auditor, and has since held several management positions. In his current role, Mr. Minks is responsible for all North American accreditations / recognitions that TÜV SÜD holds from both government and private agencies. These accreditations provide TÜV SÜD the authority to offer certifications in diverse areas such as Quality and Environmental Systems, Electrical Safety, Food Safety and Medical Device Regulations. Prior to joining TÜV SÜD America, Mr. Minks held quality management positions at several aerospace and medical device manufacturers. He graduated from the University of Massachusetts Lowell with a B.S. in Industrial Management and holds an M.B.A. from the University of Southern New Hampshire. He is also an ASQ Certified Quality Engineer (CQE), and Certified Quality Auditor (CQA). 03

Programme Outline Medical Device Seminar - Bringing your medical products to United States of America (USA) on 4 th June 2015 Time Topic 8.30 am Registration 9.00 am Welcome Address 9.15 am In the Medical Device Business and Experience Sharing Speaker: Ms. Mahsita Sari, Senior QA/RA Manager, ResMed 10.00 am Coffee Break and Networking 10.20 am Registering Your Medical Product in the US Market Speaker: Mr. Gary Minks, Vice President, TÜV SÜD America 11.10 am Medical Device Pre-Market Testing Requirements Speaker: Ms. Chua Su Chen, Product Manager, TÜV SÜD ASEAN 12.00 pm Questions and Answers 12.30 pm Lunch Break and Networking 1.30 pm Medical Device Single Audit Program (MDSAP) Speaker: Mr. Gary Minks, Vice President, TÜV SÜD America 3.30 pm Tea Break and Networking 3.50 pm Electromagnetic Compatibility (EMC) for Medical Equipment Speaker: Dr. Deng Junhong, Vice President, TÜV SÜD ASEAN 4.45 pm Questions and Answers 5:00 pm End of Programme All information is accurate at the time of printing. TÜV SÜD reserves the right to make changes to the programmes due to unforeseen circumstances. 04

Medical Device Workshop - Bringing your medical products to United States of America (USA) on 4 th June 2015 - Registration Form Complete the application form below and email to Ms. Doreen Yeo by 26 th May 2015. Tel:+65 6885 1393 / Fax: +65 6776 8670 / E-mail: doreen.yeo@tuv-sud-psb.sg Application Form: Company Name Number of Participants Company Address Telephone (Office): HP: Fax: a. Early bird discount fee Workshop fee of S$150 per person (excluding 7% GST) if registration and payment are received latest by 18 th May 2015. b. Normal registration fee Workshop fee of S$180 per person (excluding 7% GST) if registration and/or payment is received on 26 th May 2015. c. Group discount fee and Association of Medical Device Industry Singapore (AMDI) member only Workshop fee of S$120 per person (excluding 7% GST) for at least 3-5 participants from the same organization or AMDI member to register by 18 th May 2015. Enquiries Mr. Caleb Ng at DID: +65 6885 1475 or Email: caleb.ng@tuv-sud-psb.sg Payment Fax or email scanned copy of payment receipt together with registration form to guarantee your seat, or In Cheque / Cash must be made (Prior to commencement*), payable to TÜV SÜD PSB Pte Ltd is required upon registration and must be received prior to the event to guarantee your seats. Refunds and cancellations are allowed if written notice is received 14 days prior to the date of the event. No refunds are allowed thereafter. If the registered candidate is unable to attend the seminar, please inform us in writing of the replacement candidate. The final decision will be at the discretion of the management. Substitution is encouraged and permitted when notified. TÜV SÜD PSB Pte. Ltd. No. 1 Science Park Drive, 118221 Singapore Tel +65 67787777 Fax +65 6779 7088 enquiries@tuv-sud-psb.sg www.tuv-sud-psb.sg