APPLYING U.S. FDA LAWS AND REGULATIONS 2017 - Seminar on Applying U.S. FDA Laws and Regulations to Each Phase of Total Product Life Cycle (TPLC)

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Category APPLYING U.S. FDA LAWS AND REGULATIONS 2017

Deadline: February 28, 2017 | Date: March 02, 2017-March 03, 2017

Venue/Country: DoubleTree by Hilton Hotel San Francisco Airport,8, U.S.A

Updated: 2017-01-04 16:25:11 (GMT+9)

Call For Papers - CFP

This workshop style training course is supported by comprehensive knowledge of U.S. FDA laws and regulations and 30 year of extensive experience working within in the U.S. FDA regulated industries. In these 2 days, the following essential topics will be covered:

• Total Product Life Cycle and Your Medical Device

• An Overview of U.S. FDA Medical Device Regulation

• Regulations for Design and Product Development

• Premarket Notification - 510(k) and Premarket Approval (PMA)

• Regulations for Production & Process Control

• Readiness for FDA Facility Inspection

Why should you attend?

The complex network of multilayer laws, regulations and regulatory requirements create confusion and misinterpretation that leads the device manufacturer into Non-compliance state. Non-compliance to applicable laws and regulations results into severe penalties or regulatory actions form U.S. FDA that could damage image and position of the company. To avoid such undesired circumstances, it is important to see a big picture of TPLC and all applicable U.S. FDA laws and regulation at each phase of their own product life cycle.

Areas Covered in the Session:

• An Overview of U.S. FDA Regulation for Medical Devices

• Quality System Regulation 21 CFR 820: Current GMP for Medical devices

• Premarket Notification - 510(k) and Premarket Approval (PMA)

• Post Market Reporting Requirements

• FDA Facility Inspection

Who will benefit:

• Regulatory Affairs - VP, Director and Managers

• Regulatory Affairs - Associates and Specialists

• Compliance Officers

• Research & Development - Product Managers

• Quality Assurance and Quality Engineers

Agenda:

Day 1 Schedule:

Lecture 1:

Total Product Life Cycle and Your Medical Device

• Understand various definitions of Total Product Life Cycle

• Importance for define TPLC for your own medical device

• Practice Exercise: Define TPLC of your own medical device

• Building Regulatory Strategy considering TPLC

Lecture 2:

An Overview of U.S. FDA Medical Device Regulation - Part 1

Lecture 3:

An Overview of U.S. FDA Medical Device Regulation - Part 2

Lecture 4:

Regulations for Design and Product Development

• Research & Development

• Design Development and Control

• Prototype Product Development

• Design Verification

• Design Validation

• Design Transfer to Manufacturing/Production

• Helpful Hints and Suggestions

Day 2 Schedule:

Lecture 1:

Premarket Notification - 510(k) and Premarket Approval (PMA)

• Determine Class of your Medical Device for Regulatory Controls

• Exemption form Premarket and QS Regulation requirements

• Premarket Notification - 510(k)

• Premarket Approval - PMA

• Investigational Device Exemption - IDE for clinical studies

• Preparation of Premarket Submissions

• Helpful Hints and Suggestions

Lecture 2:

Regulations for Production & Process Control - Part 1

• Purchasing & Supplier Controls

• Document Control

• Device Identification and Traceability

• Acceptance & Nonconforming Product Control

• Labeling & Packaging Control

• Helpful Hints and Suggestions

Lecture 3:

Regulations for Production & Process Control - Part 2

• Corrective Action and Preventive Action (CAPA)

• Records - Device History Record, Device Master Record, QS Record

• Complaint Files including Medical device Reporting (MDR)

• Post Market Reporting Responsibilities

• Helpful Hints and Suggestions

Lecture 4:

Readiness for FDA Facility Inspection

• FDA Authority & Practices

• FDA Compliance Program Policy, Strategies and Approach

• Prepare and Stay Focused during Inspection

• Responding to FDA Form 483 Observations

• Responding to Warning Letter

• Planning and Managing Remediation Project & Activities

• Additional Regulatory Actions

Speaker:

Subhash R Patel

Subhash Patel is an accomplished Regulatory Affairs Professional offering 30 plus year of experience in authoring, preparing and submitting more than 150 successful premarket submissions to U.S. FDA. He brings his expert knowledge and hands-on experience in developing a robust premarket submission that secures clearance or approval from U.S. FDA. He offers valuable tips and suggestions on "what works and what doesn't" form his own experience. He has presented numbers of technical papers at conferences and conducted plentiful training seminars in various countries.

He is a Fellow of world's renowned Regulatory Affairs Professional Society (RAPS) and holds professional recognition as a Regulatory Affairs Certified (RAC) form RAPS. He also holds professional certification as Certified Quality Auditor (CQA) and Certified Quality Engineer (CQE) form American Society for Quality (ASQ). His educational background includes BS degree in Mechanical Engineering and BS degree in Chemistry. He founded MD Reg Consulting, LLC based in New Jersey, USA to serve medical device industry clients in all aspects of global regulatory affairs and specific to their needs.

Location: SFO, CA Date: March 2nd & 3rd, 2017 and Time: 08:30 AM to 5:00 PM

Venue: DoubleTree by Hilton Hotel San Francisco Airport

Address: 835 Airport Blvd., Burlingame CA 94010-9949

Price:

Price: $1,295.00

Until January 20, Early Bird Price: $1,295.00 From January 21 to February 28, Regular Price: $1,495.00

Register for 5 attendees Price: $3,885.00 $6,475.00 You Save: $2,590.00 (40%)*

Until January 20, Early Bird Price: $1,295.00 from January 21 to February 28, Regular Price: $1,495.00

Register now and save $200. (Early Bird)

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