Science Researcher Update | Medical Device Technology (4)

Webinar Medical Device Changes and the 510(k)

Seminar - Online

This webinar will provide valuable guidance to regulated companies in development and implementation of formal, defined, documented methods for analysis of product changes and when to file a new 510(k).

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Tags: Medical Device Technology, March, Webinar, 2015, Seminar

Webinar on If It Wasn’t Documented It Didn’t Happen: Legal & Effective Discipline & Documentation

Seminar - Online

In our litigious society, it has become more & more important for supervisors to know how to document & discipline employees to avoid law suits and manage employee performance effectively.

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Tags: Medical Device Technology, March, Healthcare, Webinar, Pharmaceuticals, 2015, Seminar

Webinar on Clean Room Design and Operation

Seminar - Online

In our litigious society, it has become more & more important for supervisors to know how to document & discipline employees to avoid law suits and manage employee performance effectively. In this program, Judi gives managers a “crash course” in safe, legal, & effective disciplinary practices & documentation.

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Tags: Medical Device Technology, March, Webinar, Pharmaceuticals, 2015, Seminar

Webinar on FDA Inspection Preparation & Readiness: The Top 20 Most Common GMP Deficiencies for Device Manufacturers

Seminar - Online

This webinar is intended to discuss FDA inspection practices and the most common deficiencies for medical device manufacturers including in vitro diagnostic device manufacturers.

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Tags: Medical Device Technology, March, Educational Event, Healthcare, Webinar, 2015, Seminar

1st Edition: International 3D Printshow Medical Conference

Conference - Berlin, Germany

Now in its fourth year of producing the industry's most original 3D printing and additive manufacture events, 3D Printshow is delighted to announce the launch of its first high-level Medical conference, which will take place on Thursday 26 March as an integral part of 3D Printshow Berlin (26, 27, 28 March 2015).

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Tags: Medical Device Technology, March, germany, Berlin, 2015, Conference

Webinar On Due-diligence & Gap Analysis in Decision Making Process for Medical Companies

Seminar - Online

In this seminar, we will discuss practical decision making steps you can follow to analyze whether to transfer or invest in keeping production in-house from a successful case study.

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Tags: Medical Device Technology, March, Healthcare, Webinar, 2015, Seminar

Webinar on Implementing an Internal Audit Program of QMA, Persisting to ISO 13485 & 21 CFR Part 820

Seminar - Online

This webinar is intended to help you adequately develop an internal audit program of a firm's quality management system (QMS) as required by ISO 13485 or 21 CFR Part 820.

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Tags: Medical Device Technology, March, Webinar, Quality Control, 2015, Seminar

2nd Annual Medical Device Product Development & Management Conference

Conference - Chicago, IL, United States

The 2nd Annual Q1 Productions Medical Device Product Development & Management Conference is a one-of-a-kind industry gathering for product management and development executives across the medical device industry, which provides executives with an unrivaled opportunity to network and share ideas and solutions to the many challenges faced in this evolving market.

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Tags: 2014, Medical Device Technology, United States, US, September, Development, Chicago, Life Sciences, Conference, IL

Webinar on Risk Analysis Tools by Global Compliance Trainings

Webinar - Online

The ISO 12971 standard on risk management for medical devices describes risk analysis tools such as PHA, FTA, FMEA, HAZOP, and HACCP but does not provide the depth needed to use the tools correctly.

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Tags: 2014, Medical Device Technology, Michigan, United States, Webinar, May, Quality Control, pharmaceutical, Life Sciences, Conference, MI

Preventing Medical Device Recalls - Global Compliance Trainings' Webinar

Conference

Preventing device recalls requires thoroughly predicting what can go wrong proactively using the risk analysis tools. Then it requires revising the specification to accommodate the mitigations for the identified failure modes and harm scenarios.

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Tags: 2014, Medical Device Technology, Michigan, United States, Healthcare, Webinar, May, Quality Control, Life Sciences, Conference, MI

Science Researcher Update Latest Posts

Science Researcher Update: Spotlight on Meetings, Conferences, and Events

Webinar Medical Device Changes and the 510(k)

Webinar on If It Wasn’t Documented It Didn’t Happen: Legal & Effective Discipline & Documentation

Webinar on Clean Room Design and Operation

Webinar on FDA Inspection Preparation & Readiness: The Top 20 Most Common GMP Deficiencies for Device Manufacturers

1st Edition: International 3D Printshow Medical Conference

Webinar On Due-diligence & Gap Analysis in Decision Making Process for Medical Companies

Webinar on Implementing an Internal Audit Program of QMA, Persisting to ISO 13485 & 21 CFR Part 820

2nd Annual Medical Device Product Development & Management Conference

Webinar on Risk Analysis Tools by Global Compliance Trainings

Preventing Medical Device Recalls - Global Compliance Trainings' Webinar

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