Events in the next 30 days

Best Practices for Maintaining an IND and IDE

This webinar on IND and IDE Application management will help you understand the current FDA requirements for IND and IDE application post initial approval to proceed with the clinical trial.

Medical Device Alarms to Mitigate New FDA Concerns

This webinar on alarms in patient monitoring devices will show how you can address FDA concerns regarding alarm standards and safety.

Medical Device Complaints, MDR’s and Recalls

Medical device firms need to be aware of the benefits of compliance as well as the dangers of inadequate complaint handling.

HIPAA Privacy, Security and Breach Notification

HIPAA Privacy, Security and Breach Notification Compliance: Understanding the Requirements, Preventing Incidents, Surviving Audits, and Avoiding Penalties - US Seminar 2012 at Boston

International Terms 2010 Rules

Learn and understand the rules for international terms of sale; save pages of contract information by use of the proper rule.

Controls to Meet Tougher U.S FDA Requirements

This 90-minute webinar on supplier controls will help you refine your supplier management and audits to match the FDA's tougher position.

Import Compliance- How to Reduce Your Import Risks

By lowering the import risks to your suply chain would lead to fewer Customs inspections and delays to your freight. The reduce lead times would enhance cost savings.

Water System Biofilm Control and Microbial Monitor

Water System Biofilm Control and Microbial Monitoring Myths - Webinar By GlobalCompliancePanel

21 CFR Part 11: How to Successfully Prepare for an

Short and quick overview of the Part 11 regulation; detailed description of HOW TO prepare for an FDA inspection when and where Part 11 is in scope or the scope of the inspection

DHF, DMR, DHR, Technical File and Design Dossier

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

Preparing for HIPAA Compliance Audits: What they w

Find out what HHS OCR is likely to ask you if you are selected for an audit, and what you'll have to have prepared already when they do.

Risk Analysis Techniques in Clinical Trials

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.

Statistics for the Non-Statistician

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

Validation of Analytical Methods for FDACompliance

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

What does Sarbanes-Oxley, Dodd-Frank and Hedging F

The subject of risk compliance and 'are you prepared' is being discussed far more frequently (using platforms like webinars and white-paper downloads)

What does Sarbanes-Oxley, Dodd-Frank and Hedging F

The topic aims to address and compare the requirements of SOX against the Dodd-Frank legislation and contrast how they differ clearly in purpose and objectives.

Best Technique for Clinical Trial Audit,Inspection

This webinar on clinical trial audit/ inspection preparedness will discuss in detail about applicable regulatory and sponsor requirements, guidelines and SOPs.

(3 days)

Big Design Conference 2012

Join experts in the fields of design, mobile, gaming, usability, strategy, content, multimedia, and film in Big D.

Preparing for FDA Inspection and Handling the Cons

We will review the latest inspection statistics released from FDA, discuss how to prepare for an FDA Inspection,

Device Corrections and Removals

This 90-minute webinar on device corrections and removals will clarify your obligations for corrections and removals under Part 806 of the FDA regulations.

Verification and Validation in the Medical Devices

This 90-minute presentation will cover the FDA Quality System Requirements for software used in medical devices.

FDA Acceptance of non-US Clinical Trials

This webinar will help you understand how non-IND clinical trials at non-US locations can be used successfully to support an IND/IDE or a marketing approval application.

Medical Device - Mitigation through FMEA

This 90-minute presentation will discuss a structured way to mitigate risks with minimum cost. You will learn how to use FMEA to effectively estimate and assess risks in your medical device.

An Approach to Fair Lending and UDAAP

Current and future compliance professionals, lenders, loan originators, board of directors, senior management. Anyone responsible for the development, marketing, and sales of bank products .

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