Listings for Health Webinars (210)

Logo with tag and trademarks
Logo with tag and trademarks

With the recently proposed budget cuts to medical research, now is the time to be aware and increase the voice of those impacted by these policy decisions. Kick...

Elements of a CAPA System and Uses of CAPA Data
Elements of a CAPA System and Uses of CAPA Data

$150.00

Overview: FDA offers some relief from the strict requirements if you participate in a voluntary Affirmation of Compliance (AOC). Providing accurate informatio...

Software Validation for the New FDA Inspections
Software Validation for the New FDA Inspections

$150.00

Overview: This course will teach how to conduct a software validation program that will satisfy FDA requirements and produce a safe product. Why should you ...

SOP Development and Implementation for the Regulated Industry
SOP Development and Implementation for the Regulated Industry

$150.00

Overview: This workshop will explore what SOPs are, what they are used for, when they are required, how to write them effectively for compliance and for implem...

abhishek
abhishek

Description When it comes to federal and state laws, there can be some notions and articles that are challenging to understand and keep up with.This webinar wi...

Medical Device Employee Training -Requirements and Implementation tips
Medical Device Employee Training -Requirements and Implementation tips

$150.00

Overview: This is especially true for start-up and other small medical device companies, or rapidly growing companies. Specific FDA training requirements wil...

Phase I GMPs
Phase I GMPs

$150.00

Overview: Early clinical trials are conducted to establish initial safety of a drug. The studies are generally in small number of healthy subjects and use lo...

How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare
How FDA Trains its Investigators to Review CAPA and What You Should Do to Prepare

$150.00

Overview: In this session will be a section-by-section summary of the CAPA subsection of the QSIT, the document by which FDA inspectors operate during an ins...

Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations
Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations

$150.00

Overview: This webinar will discuss FDA's current recommendations on using electronic health records in prospective clinical investigations of human drugs, bio...

Good Deviation Practice What you need to know
Good Deviation Practice What you need to know

$150.00

Overview: This course explores the deviation and CAPA processes and best practices for both. It shows how to avoid pitfalls and minimize regulatory scrutiny by...

Supplier Evaluation and Assessment How to Meet FDA QSR and ISO 13485 Requirements in a Cost-Effective Manner
Supplier Evaluation and Assessment How to Meet FDA QSR and ISO 13485 Requirements in a Cost-Effective Manner

$150.00

Overview: A lack of adequate control over purchases has resulted in a significant number of recalls due to component failures. Since FDA does not directly regu...

Anjali Mukerjee Live Webinar
Anjali Mukerjee Live Webinar

Attend Live Webinar by Anjali Mukerjee on 9th & 18th March, 2017 and get a chance to get your questions answered on Weight Loss, Obesity & lifestyle dis...

FDA Regulations for Analytical Instrument Qualification and Validation Processes
FDA Regulations for Analytical Instrument Qualification and Validation Processes

$150.00

Overview: In this webinar you will learn the different global agencies expectations of analytical equipment qualification along with the development of a sou...

Efficient and Effective FDA and ISO Management Reviews
Efficient and Effective FDA and ISO Management Reviews

$150.00

Overview: In this presentation will cover the requirement for management review from FDA cGMP and ISO 13485 and approaches that can make these effective. Man...

How to Conduct a Human Factors - Usability Validation Test following ISO 62366 and the 2016 FDA Guidance
How to Conduct a Human Factors - Usability Validation Test following ISO 62366 and the 2016 FDA Guidance

$150.00

Overview: This webinar will explain the procedure described in ISO62366 and the 2016 FDA Guidance for a compliant human factors/ usability validation. HF/U v...

Pharmaceutical and Biologics Facility Design FDA and Regulatory Aspects
Pharmaceutical and Biologics Facility Design FDA and Regulatory Aspects

$150.00

Overview: This course explores some of the best practices of pharmaceutical facility design with an emphasis on regulatory aspects. FDA and other global regu...

Real World Statistics What to Do When It's Not a Bell Curve
Real World Statistics What to Do When It's Not a Bell Curve

$150.00

Overview: Statistical textbooks, manuals, and even most software rely on the assumption that processes conform to the normal or bell curve distribution. W...

Auto Draft
Auto Draft

The Healthcare practice at MarketsandMarkets is pleased to announce its Webinar on the "In situ Hybridization Market by Technique (FISH, CISH), Application (Can...

FB_IMG_1486581307977
FB_IMG_1486581307977

Learn how to take control of your health! We will discuss your future health, waist size, gut health, nutrition and how to get more energy! Tuesday, February...

Paras Hospital Gurgaon
Paras Hospital Gurgaon

Dr Minakshi Saxena, Chief Coordinator – Mother & Child, Paras Hospitals, Gurgaon is talking about the importance of Breastfeeding for both Mother and Child....

images
images

If you are looking to improve your memory a little bit, then use the knowledge that you have by teaching others Cognishield Doing this makes your brain fire in ...

Switzerland May -Applying ISO14971 and IEC62304
Switzerland May -Applying ISO14971 and IEC62304

$1,695.00

Overview: Gaps, incorrect or incomplete implementation of safety functionality can delay or make the certification/approval of medical products impossible. Mo...

Switzerland April -Supplier Management for Medical Device Manufacturers
Switzerland April -Supplier Management for Medical Device Manufacturers

$1,695.00

Overview: Supplier selection and management is one of the critical issues for medical device manufacturers. Suppliers provide materials and services to the dev...

Crooked Neck
Crooked Neck

Poor ergonomics can lead to pain, fatigue, loss of sensation and a reduction in overall performance. Furthermore, it can cause serious musculoskeletal disorders...

Tissue-Banking-Market_102016_024744
Tissue-Banking-Market_102016_024744

Enabling quality successful future research and contributing to the growing evolution of regenerative medicine in any form is the primary aid enjoyed by the tis...

LisaFinely-Webcast-Slider-012317
LisaFinely-Webcast-Slider-012317

Join us as we discuss how the tools of mindfulness, motivational interviewing, cognitive behavior therapy, coaching and nonviolent communication promote healing...

18 Compliance Boot Camp
18 Compliance Boot Camp

$1,295.00

Course "Compliance Boot Camp" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. ...

17 Supplier Management for Medical Device Manufacturers 2017
17 Supplier Management for Medical Device Manufacturers 2017

$1,295.00

Course "Supplier Management for Medical Device Manufacturers" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recerti...

16 HIPAA Survival - All you need to Know
16 HIPAA Survival - All you need to Know

$1,295.00

Overview: This seminar will be addressing how practice/business managers (or compliance offers) need to get their HIPAA house in order before the imminent audit...

13 Validation, Verification and Transfer of Analytical Methods 2017
13 Validation, Verification and Transfer of Analytical Methods 2017

$1,695.00

Overview: Analytical methods and procedures should be validated to ensure reliability, consistency and accuracy of analytical data. Compendial methods should b...

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