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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
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 »
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

Statistics for the Non-Statistician - US Seminar 2012 at Washington DC

Conference |Courtyard by Marriott Washington, DC, Washington, DC, USA
May 24, 2012 | 0 people are attending

Overview: This course will help you to use statistics correctly and minimize compliance risk. 

Organizer: 
GlobalCompliancePanel
More information about Statistics for the Non-Statistician - US Seminar 2012 at Washington DC »
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
30

21 CFR Part 11 compliance for Electronic Medical Records

Webinar |Online Webinar, Palo Alto, CA, USA
May 30, 2012 | 0 people are attending

This 21 CFR Part 11 training will analyze the regulations and provides concrete guidance on compliance for Electronic Medical Records.

Electronic Medical Records are the future. Some facilities and doctors are already using this cutting edge technology, and the medical community in general is moving in this direction.

Organizer: 
ComplianceOnline
More information about 21 CFR Part 11 compliance for Electronic Medical Records »
May
30

Avoiding the fines and costs of healthcare information breaches and what to do when you have a breach - Webinar By ComplianceOnline

Webinar |Online Webinar, Palo Alto, CA, USA
May 30, 2012 | 0 people are attending

This 90-minute webinar on HIPAA Breach Notification will show how to create an effective breach notification policy for your organization and how to follow through when a breach occurs. You will learn about the kinds of threats that exist for PHI, information security methods you can use to keep breaches from happening, and be in compliance with the HIPAA Security Rule as well.

Why Should You Attend:

Organizer: 
ComplianceOnline
More information about Avoiding the fines and costs of healthcare information breaches and what to do when you have a breach - Webinar By ComplianceOnline »
May
31

What Are the Current Tools and Best Techniques for (Clinical Trial) Audit/Inspection Preparedness?-Webinar By ComplianceOnline

Webinar |Online Webinar, Palo Alto, CA, USA
May 31, 2012 | 0 people are attending

This webinar on clinical trial audit/ inspection preparedness will discuss in detail about applicable regulatory and sponsor requirements, guidelines and SOPs, and how you can ensure that the conduct of clinical research at the investigative site(s) complies with them.

Why Should You Attend:

Organizer: 
ComplianceOnline
More information about What Are the Current Tools and Best Techniques for (Clinical Trial) Audit/Inspection Preparedness?-Webinar By ComplianceOnline »
May
31

3-hr Virtual Seminar: GMP Compliant Stability Program for Pharmaceuticals

Webinar |OnlineEvent, Palo Alto, CA, USA
May 31, 2012 | 0 people are attending

This 3-hr virtual session will cover pharmaceutical stability study requirements for Phase I, Phase II, Phase III clinical studies, show how to choose the right stability methods and specifications and review common pitfalls in pharmaceutical stability programs.

Description 

Why Should You Attend:

Organizer: 
ComplianceOnline
More information about 3-hr Virtual Seminar: GMP Compliant Stability Program for Pharmaceuticals »

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