Online event

Online event
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June 21, 2010

Quality Assurance in e-Governance-Online at Online event

June 30, 2010

Overcoming Your Fear & Of Addictions Call with Greg Woodhill, M.A. at Online event

October 3, 2010

Autumn Sale! House of Walker Publishing at Online event

August 24, 2011

Becoming a Hands On IT Business Analyst at Online event

August 31, 2011

Business Analysis - part I at Online event

September 6, 2011

The Economist's Online MBA Fair - Free at Online event

March 13, 2012

Free Tech Webinar: PMI Agile Certification at Online event

August 21, 2012

GlobalEye Affiliate Program Launch at Online event

October 31, 2012

Construct and Manage the Technical File and Design Dossier - Webinar By GlobalCompliancePanel at Online event

November 7, 2012

Medical Device Recalls and Regulatory Enforcement at Online event

November 8, 2012

Quality Risk Management Overview for Pharma and Biopharma, ICH Q9/ISO 14971 at Online event

November 12, 2012

Long-term Preservation of Records Needed for Drug Regulatory Compliance at Online event

November 13, 2012

3-hr Virtual Seminar: Strategies for Preparing a Successful 510(k) Premarket Notification for FDA Submission at Online event

November 14, 2012

Drug Utilization vs Registry Studies – Differences and regulatory requirements at Online event

November 14, 2012

Full Day Virtual Webinar: Medical Device Process Validation - FDA Inspectors are Checking – Are You Prepared? at Online event

November 14, 2012

Supplier Quality Assurance Agreements: Why a General Supply Agreement May Not Be Enough with Some Suppliers at Online event

November 20, 2012

Proposed Changes in the European Medical Device Directive 2012/0266 (COD): A Practical Approach to the New Regulations at Online event

November 27, 2012

Establishing Effective Employee Training Programs for Medical Device Companies: What Works and What Doesn’t at Online event

November 27, 2012

Quality Assurance During a Clinical Trial at Online event

December 3, 2012

Personnel Practices and Microbial Control in Pharmaceutical, Biotech, and Medical Device Manufacturing at Online event

December 3, 2012

Medical Foods: Understanding what Constitutes a Medical Food for FDA Regulatory Purposes and Strategies for Successfully Commercializing such Products in the U.S. at Online event

December 4, 2012

FDA’s Regulation of Unique Device Identification (UDI) - Are you Prepared? at Online event

December 4, 2012

Understanding Expanded Access for Medical Devices at Online event

December 4, 2012

Throwing the Data Over the Wall: Why No One Knows the Quality of the Clinical Data at Online event

December 6, 2012

Quality Assurance at the (Clinical Research) Site: How to Develop a Manageable Plan at Online event

December 11, 2012

Deviations: What are they? Do you need to report? at Online event

December 11, 2012

The Fundamentals of Accounts Receivable Collection Techniques at Online event

December 12, 2012

Computerized System Validation - A Detailed Insight at Online event

December 12, 2012

The Informed Consent Process at the Investigator Site- Who decides if it is adequate and GCP compliant, Ethics Committee, Sponsor, or Investigator? at Online event

December 12, 2012

Patient Reported Outcomes (PROs): Overview and Guidance for clinical trials and medical product labeling at Online event

December 12, 2012

Internal Controls in Purchases, Accounts Payable and Payment at Online event

December 12, 2012

Reducing eDiscovery risk for Pharmaceutical Companies at Online event

December 19, 2012

Modifications to a Cleared Device - FDA’s 510(k) Guidance at Online event

January 6, 2013

How to Obtain a Canadian Medical Device License at Online event

January 9, 2013

Sampling Plans for (FDA) Quality Audits at Online event

January 14, 2013

Essentials of Sterilizing Grade Filter Validation at Online event

January 14, 2013

3-hr Virtual Seminar: Latin America – Understanding Regulatory Compliance Requirements Across the Life Science Industry at Online event

January 15, 2013

Optimal Clinical Supply Planning for Global Drug Development at Online event

January 17, 2013

Implementing Risk-based Verification for Pharmaceutical Manufacturing Companies at Online event

January 21, 2013

Bad Debt Forecasting: Two Methods to Accurately Calculate Future Trade Credit Losses at Online event

January 22, 2013

Superiority, Non-inferiority, or Equivalence Trials: How, Why and When at Online event

January 23, 2013

Negotiating Clinical Trial Contracts in a Minefield: The Stark Rule, Anti-kickback Statute (AKS), False Claims Act (FCA) and Medicare Secondary Payer Rule (MSPR) at Online event

January 28, 2013

IFRS and U.S. GAAP Classification Inconsistencies in the Statement of Cash Flows at Online event

February 11, 2013

How to Achieve CMDCAS Certification (For Medical Device Companies That Want to Sell in Canada) at Online event

February 18, 2013

Reformulating IFRS and US GAAP Statements of Cash Flows for Financial Analysis at Online event

February 20, 2013

How to Identify and Successfully Sell on Credit to High Risk Commercial Customers at Online event

February 20, 2013

3-hr Virtual Seminar: South East Asia Regulatory Compliance for Life Science Products - Hong Kong, Taiwan, Thailand, Singapore, Malaysia and Vietnam at Online event

March 18, 2013

Creating a Trade Credit Policy to Maximize Cash Flow While Minimizing Bad Debt at Online event

March 25, 2013

Operating vs. Non-operating Items in the Statement of Comprehensive Income under IFRS and U.S. GAAP at Online event

April 15, 2013

Dietary Supplements - Regulatory Compliance Requirements, Product Claims, Labeling Issues and FDA Updates at Online event

April 15, 2013

21 CFR Part 11 and Annex 11 Compliance; specifics needed to eliminate 483s at Online event

April 22, 2013

China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations) at Online event

April 25, 2013

Gaining and Re-Establishing Control of Your Cleanroom at Online event