ComplianceOnline

Event organizers, Biotechnology / R&D services

Get trained on regulations affecting your industry through online webinars, learn the best practices, and download quality standards, checklists and news articles. Listen to experts on best practices to streamline quality and compliance processes and meet the regulatory demands.

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Upcoming events

May
22

Supplier Controls to Meet Tougher U.S. FDA Requirements - Webinar By ComplianceOnline

Webinar |Online Webinar, Palo Alto, CA, USA
May 22, 2012 | 0 people are attending

This 90-minute webinar on supplier controls will help you refine your supplier management and audits to match the FDA's tougher position. We will evaluate the chief areas of change to see how to better prepare a supplier chain management and audit program.

Organizer: 
ComplianceOnline
More information about Supplier Controls to Meet Tougher U.S. FDA Requirements - Webinar By ComplianceOnline »
May
22

OSHA's Update of Hazard Communication - Webinar By ComplianceOnline

Webinar |Online Webinar, Palo Alto, CA, USA
May 22, 2012 | 0 people are attending

This 90-minute webinar will cover the OSHA’s new Hazard Communication Standard and will discuss the differences between the old standard and the new standard so that attendees will be able to adapt and apply the requirements in the workplace.

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ComplianceOnline
More information about OSHA's Update of Hazard Communication - 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

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

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.

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

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

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

The A to Z’s of Microbial Control, Monitoring and validation of Pharmaceutical Water Systems

Conference |Renaissance Newark Airport Hotel 1000 Spring Street, Elizabeth, New Jersey, United States
May 24, 2012 - May 25, 2012 | 0 people are attending

Course Description :

Organizer: 
ComplianceOnline
More information about The A to Z’s of Microbial Control, Monitoring and validation of Pharmaceutical Water Systems »
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.

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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
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 »

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