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May
23

Best Practices for Medical Device Reporting (MDR), Recall, Reports of Corrections and Removals

Webinar |OnlineEvent, Palo Alto, CA, USA
May 23, 2012 | 0 people are attending

This 90-minute webinar will discuss the requirements and compliance under the applicable FDA regulations for medical device reporting (MDR), recall and reports of corrections and removals in the US. It is designed to help the audience develop, maintain and implement adequate procedures.

Description 

Why Should You Attend:

Organizer: 
ComplianceOnline
More information about Best Practices for Medical Device Reporting (MDR), Recall, Reports of Corrections and Removals »
May
23

Validation of Existing/ Legacy Computer Systems for FDA/EU Compliance-Webinar By ComplianceOnline

Webinar |Online Webinar, Palo Alto, CA, USA
May 23, 2012 | 0 people are attending

This webinar on validating legacy computer systems will give a good understanding of FDA and EU regulatory requirements for validation (retrospective validation) and provide tools for effective implementation.

Why Should You Attend:

Organizer: 
ComplianceOnline
More information about Validation of Existing/ Legacy Computer Systems for FDA/EU Compliance-Webinar By ComplianceOnline »
May
23

FDA Warning Letter - Consent Decree Software Validation - Webinar By ComplianceOnline

Webinar |Online Event, Palo Alto, CA, United States
May 23, 2012 | 0 people are attending

This FDA warning letter Webinar/training will discuss what to do to avoid additional software related compliance along with the response steps where the citations that directly or indirectly include automated system.

Areas Covered in the seminar:

Organizer: 
ComplianceOnline
More information about FDA Warning Letter - Consent Decree Software Validation - Webinar By ComplianceOnline »
May
23

Live webinar on21 CFR Part 11: How to Successfully Prepare for and Host an FDA Inspection - Primer For Success By Compliance2go

Webinar |Online, Houston, Texas, United States of America
May 23, 2012 | 0 people are attending

Short and quick overview of the Part 11 regulation; detailed description ofHOW TO prepare for an FDA inspection when and where Part 11 is in scope or the scope of the inspection; detailed description of HOW TO handle the FDA inspection during the inspection itself; some trends when it comes to Part 11 inspections; commonly asked questions; warnning letters examples; and what the future holds when it comes to Part 11.

 

Why should you attend

 

Organizer: 
compliance2go
More information about Live webinar on21 CFR Part 11: How to Successfully Prepare for and Host an FDA Inspection - Primer For Success By Compliance2go »
May
23

DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel

Webinar |Online Training, Wilmington, United States
May 23, 2012 | 0 people are attending

Overview: This webinar will examine the existing and proposed requirements for the FDA's DHF - including its derivative documents, the DMR and DHR. It will consider the MDD's TF/DD requirements, and evaluate the documents' differing purposes / goals. 

Organizer: 
GlobalCompliancePanel
More information about DHF, DMR, DHR, Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel »
May
24

Risk Management and Risk Analysis Techniques in Clinical Trials-Webinar By ComplianceOnline

Webinar |Online Webinar, Palo Alto, CA, USA
May 24, 2012 | 0 people are attending

This webinar will provide you with an overview of risk factors in clinical trials and discuss possible ways to mitigate, control, assess impact, and prevent them in your trial.

Why Should You Attend:

Organizer: 
ComplianceOnline
More information about Risk Management and Risk Analysis Techniques in Clinical Trials-Webinar By ComplianceOnline »
May
24

Configuration Management and Change Control for Networks and Computer Systems

Webinar |Online, Online, United States
May 24, 2012 | 1 people are attending

This seminar will discuss how to control changes of hardware, firmware, software and documentation of computer systems and netorks

Why to attend:
   

Organizer: 
Labcompliance
More information about Configuration Management and Change Control for Networks and Computer Systems »
May
24

Validation of Analytical Methods for FDA Compliance: Step-by-Step - Webinar By GlobalCompliancePanel

Webinar |Online Training, Wilmington, United States
May 24, 2012 | 0 people are attending

Overview: Analytical methods should be validated to ensure reliability, consistency and accuracy of analytical data. Method validation has been a requirement of FDA and international regulations and accreditation standards such as ISO 17025 since many years. Most often the theory is well understood but there are many questions when validation experiments are designed, conducted, and documented. 

Organizer: 
GlobalCompliancePanel
More information about Validation of Analytical Methods for FDA Compliance: Step-by-Step - Webinar By GlobalCompliancePanel »
May
24

Pre-Approval Statements and Representations by Pharmaceutical Manufacturers-Webinar By ComplianceOnline

Webinar |Online Webinar, Palo Alto, CA, USA
May 24, 2012 | 0 people are attending

This 90-minute webinar will help you understand the problems that can occur with statements by pharmaceutical manufacturers directed to off-label uses of pharmaceuticals.

Why Should You Attend:

Organizer: 
ComplianceOnline
More information about Pre-Approval Statements and Representations by Pharmaceutical Manufacturers-Webinar By ComplianceOnline »
May
24

3-hr Virtual Seminar - Affirmative Action Compliance and Your Recruiting Strategy: Pulling it together

Webinar |OnlineEvent, Palo Alto, CA, USA
May 24, 2012 | 0 people are attending

This 3-hr virtual seminar will take a deeper look at your recruiting practice and review the objective for affirmative action as it relates to this function in terms of ensuring compliance. The session also features a discussion about how to make the most of your recruiting technology so that you are prepared to meet the OFCCP’s recently heightened enforcement efforts.

Description 

Why Should You Attend:

Organizer: 
ComplianceOnline
More information about 3-hr Virtual Seminar - Affirmative Action Compliance and Your Recruiting Strategy: Pulling it together »

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