complianceonlinecom #1225327

April 28, 2011

Full-day In-person Seminar - Key GMP Systems in Pharmaceutical and Biotech Labs at Hampton Inn Philadelphia-International Airport

June 12, 2011

2-day in-person seminar - Integrated Risk Management and Medical Device QMS - Are You Ready For Increased Regulatory Scrutiny? at Sheraton DFW Airport Hotel

May 24, 2012

The A to Z's of Microbial Control, Monitoring and validation of Pharmaceutical Water Systems - Seminar By ComplianceOnline at Renaissance Newark Airport Hotel

June 6, 2012

Unsolicited Drug and Device Off-Label Claims Via Social Media and Risk Management at Online Event worldwide

June 6, 2012

Navigating the Japan and South Korean Regulatory Compliance and Clinical Trial Environment - Seminar By ComplianceOnline at Hyatt Regency Columbus Ohio

June 6, 2012

Verification and Validation (V&V) of Software in the Medical Devices at Online Event worldwide

June 8, 2012

3-hr Virtual Seminar: Legal Issues Impacting Human Resource Management at Online Event worldwide

June 13, 2012

Promoting and Advertising Dietary Supplements in Compliance with FDA and FTC Regulations at Online Event worldwide

June 13, 2012

3-hr Virtual Seminar: The Psychology (and Law) of Harassment Investigations at Online Event worldwide

June 14, 2012

2-day In-person Seminar: Medical Device Sterilization: Corrective & Preventive Action at Hyatt Regency Irvine

June 14, 2012

REMS Update: Risk Evaluation and Mitigation Strategies at Online Event worldwide

June 14, 2012

Common Concerns and Penalties Related to the Americans with Disability Amendments Act (ADAA) at Online Event worldwide

June 14, 2012

Auditing Systems for 21 CFR Part 11 Compliance: Preparing Yourself for Inspection at Online Event worldwide

June 15, 2012

The Investigational Medicinal Product Dossier (IMPD): EU's CTA vs. FDA's IND at Online Event worldwide

June 19, 2012

Complying with FLSA – How to Determine Exempt Status & Calculate Overtime Correctly at Online Event worldwide

June 19, 2012

The U.S. FDA's New Global Engagement Initiative - Webinar By ComplianceOnline at Online Event worldwide

June 19, 2012

Thriving on Risk – Risk Management for 21st Century - Seminar By ComplianceOnline at Grand Hyatt San Francisco

June 19, 2012

Medical Device: Risk Assessment and Mitigation through FMEA at Online Event worldwide

June 20, 2012

An Introduction to Process Validation - For Beginners at Online Event worldwide

June 21, 2012

Computer System Validation - Reduce Costs and Avoid 483s - Seminar By ComplianceOnline at Omni San Diego Hotel

June 21, 2012

How FDA Trains Its Investigators to Review CAPA, and What You Can do to Prepare at Online Event worldwide

June 22, 2012

Acceptance Sampling by Variables Using Z1.9 - Webinar By ComplianceOnline at Online Event worldwide

June 25, 2012

Ethics and Privilege Issues Under ERISA - Webinar By ComplianceOnline at Online Event worldwide

June 26, 2012

cGMPs for Medical Devices, Including In Vitro Diagnostic Devices at Online Event worldwide

June 28, 2012

Obtaining and Marketing Your 510(k) with Today's FDA, a 510(k) Workshop - Seminar By ComplianceOnline at Grand Hyatt San Francisco

June 28, 2012

Telecommuting: Effective Policies, Practices, and Programs at Online Event worldwide

June 28, 2012

FDA’s Regulation of Veterinary Regenerative Medicine at Online Event worldwide

June 28, 2012

Understanding and Effectively Controlling Biofilm in Pharmaceutical Water Systems at Online Event worldwide

June 29, 2012

Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs at Online Event worldwide

June 29, 2012

3-hr Virtual Seminar: IND Applications for Phase I Studies at Online Event worldwide

July 2, 2012

Affirmative Action and Recent Trends within the OFCCP - Webinar By ComplianceOnline at Online Event worldwide

July 12, 2012

Supplier Management for FDA Compliance at Online Event

July 12, 2012

Gaining and Re-Establishing Control of Your Cleanroom - Webinar By ComplianceOnline at Online Event

July 18, 2012

An Introduction to FDA’s Regulation of Over-the-Counter (OTC) Drug Products at Online Event

July 18, 2012

Understanding and Implementing the Medical Device Directive - Seminar By ComplianceOnline at Courtyard Philadelphia Downtown

July 19, 2012

Designing an Effective Cleaning Validation for Reusable Medical Devices in Today's Regulatory Environment at Online Event

July 24, 2012

ICH Q10; moving from GMPs to a Pharmaceutical Quality System at Online Event

July 25, 2012

3-hr Virtual Seminar: Latin America – Understanding Regulatory Compliance Requirements at Online Event

July 26, 2012

FDA Compliant GLP for Nonclinical Studies - For Pharmaceutical and Medical Device Industries at Orlando Airport Marriot

July 26, 2012

Best Practices in Document Approval, Control, and Distribution at Online Event

July 31, 2012

Maximizing ROI on Each Compliance Effort - Webinar By ComplianceOnline at Online Event

August 3, 2012

Making Sense of FDA’s (proposed) Rules for the Development and Approval of Biosimilars at Online Event

August 7, 2012

How To Establish An Effective Good Clinical Practice in Drugs and Medical Devices at Online Event

August 14, 2012

Biomarkers for Drug Development at Online Event worldwide

August 15, 2012

The Nature of e-Banking, a Precursor to Understanding its Compliance & Risks at Online Event

August 16, 2012

CAPA Systems for Medical Device Manufacturers - Seminar By ComplianceOnline at Grand Hyatt San Francisco

August 16, 2012

The Credit Risk Management System and Credit Industry Groups - Webinar By ComplianceOnline at Online Event

August 16, 2012

Updating Compliance for Design History Files of Older Products at Online Event worldwide

August 16, 2012

Fraud - A Lightning Overview at Online Event

August 16, 2012

Container Closure Systems for Liquid and Lyophilized Products - Webinar By ComplianceOnline at Online Event

August 20, 2012

Dietary Supplement Regulatory Compliance in the United States: Labeling, Product Claims & Updates from the FDA at Online Event worldwide

August 21, 2012

Process Verification and Validation Planning and Execution at Online Event worldwide

August 21, 2012

Disinfectant Qualification and Cleanroom Disinfection at Online Event worldwide

August 22, 2012

Addressing Impurities in Pharmaceutical Products: Impurities, Degradants, Residual Solvents and Elemental Impurities at Online Event worldwide

August 22, 2012

Top 20 Internal Controls to Detect and Prevent Fraud at Online Event

August 22, 2012

The 6 Most Common Problems in FDA Software Validation & Verification at Online Event worldwide

August 23, 2012

2-day In-person Seminar: FDA’s GMP Expectations for Phase I and First-in-Man Clinical Trials at Hampton Inn Philadelphia City Center

August 23, 2012

21CFR Part 11 and Harmonization with 21 CFR Part 812 for Medical Device Trials at Online Event

August 23, 2012

Laboratory Inspections – Be Prepared, Be Validated and Avoid Observations - Seminar By ComplianceOnline at Sheraton San Diego Hotel and Marina

August 23, 2012

Anticipated Changes to the EU Medical Device Directives; 2010 Changes and What the Future Holds for Licensees at Online Event worldwide

August 23, 2012

Export Letters Of Credit - Webinar By ComplianceOnline at Online Event

August 23, 2012

People Metrics and Human Capital Risk Management - Webinar By ComplianceOnline at Online Event

August 24, 2012

Verification vs. Validation in Regulated Industries at Online Event

August 27, 2012

Site Challenges in Conducting Investigational Device Trials at Online Event worldwide

August 28, 2012

Risk Management for Business Financing at Online Event

August 28, 2012

Risk Management for Directors and Officers at Online Event

August 28, 2012

Strategies for Preparing and Submitting Successful Citizen Petitions and Suitability Petitions to FDA at Online Event

August 28, 2012

Characterization and Comparability Testing of Biosimilars (Biosimilar Analytics) at Online Event

August 28, 2012

Laboratory Water Quality at Online Event worldwide

August 29, 2012

(QMS) Competence and Training Requirements per FDA QSR and ISO 13485 at Online Event worldwide

August 31, 2012

Reducing Ethylene Oxide (EO) Sterilization Costs While Maintaining Regulatory Compliance at Online Event worldwide

September 5, 2012

Validation and use of Excel spreadsheets in FDA regulated environments at Online Event worldwide

September 6, 2012

How to Investigate Environmental Monitoring Excursion Limits at Online Event worldwide

September 6, 2012

Quality Assurance at the (Clinical Research) Site at Online Event

September 12, 2012

Key Elements in Managing Operational Risk at Online Event

September 12, 2012

Stability Studies for Vaccine Products at Online Event

September 13, 2012

China & Pacific Rim Markets : Compliance Processes for Life Science Products - Seminar By ComplianceOnline at Grand Hyatt San Francisco

September 20, 2012

Understanding the Different Operational Risks at Online Event

October 11, 2012

2-day In-person Seminar: Preparing IND Submissions for Conventional and Orphan Products at Hampton Inn Philadelphia City Center

October 24, 2012

International Credit and Debt Collection Challenges at Online Event

October 26, 2012

When does GCP Non-compliance at an investigator site compromise a regulatory submission? at Online Event

October 26, 2012

Interpreting FDA’s New Guidance Document on Risk-based Monitoring at Online Event

October 30, 2012

Class-action Litigation - What Risk Managers and Business Leaders Need to Know at Online Event

November 1, 2012

Employee Expense Reimbursement Fraud: Detection, Prevention and Deterrence at Online Event

November 1, 2012

Non-inferiority Trials: Practical Issues and Current Regulatory Perspectives at Online Event worldwide

November 1, 2012

An Interactive Workshop on Premarket [510(k)] Notification Submissions at Grand Hyatt San Francisco

November 6, 2012

Roles and Responsibilities of a New Clinical Monitor Assistant (CMA) at Online Event

November 7, 2012

A Cost/Benefit Framework for Making Rational Insurance Risk Retention Decisions at Online Event

November 7, 2012

Preparing for FDA GCP Inspections – Essentials for Sponsor Companies at Online Event

November 7, 2012

Risk Mitigation and Optimization Techniques for Drug Development Portfolio Planning at Online Event worldwide

November 7, 2012

Preparing for FDA GCP Inspections – Essentials for Sponsor Companies 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 8, 2012

Contamination-Control and Cleaning and Disinfection at Tampa International Airport

November 9, 2012

South Korea - Navigating the South Korean Regulatory Compliance and Clinical Trial Environment at Online Event worldwide

November 9, 2012

Data Monitoring: Meeting the Needs and Requirements of Sponsors and IRBs at Online Event worldwide

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

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 14, 2012

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

November 14, 2012

Risk-based Monitoring Within a Clinical Quality Management System at Online Event

November 14, 2012

Latin America: Regulatory Compliance Requirements for Life Science Products at Boston Marriott Copley Place

November 16, 2012

Assessing your Investigator Site for GCP Non-compliance at Online Event

November 20, 2012

Dispelling the Myths About Clinical Standardization 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

3-hr Virtual Seminar: Addiction in the Workplace, Legal Issues, and Practical Solutions 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

November 28, 2012

IT Auditing - Principles and Practices for Executives and Directors at Online Event

November 28, 2012

Employees vs. Independent Contractors – Understanding Legal Differences and Staying Compliant at Online Event

November 28, 2012

Practical strategies to Improve Productivity in the Pharmaceutical Laboratory at Online Event

November 29, 2012

Understanding the New USP Chapter for Transfer of Analytical Methods at Online Event

November 30, 2012

Trade Compliance Automation – Export Compliance Screening at Online Event

November 30, 2012

Confined Space Entry Permit Program - OSHA Regulation 29 CFR 1910.146 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

OSHA Fall Protection Program: 29 CFR 1926.500 – 503 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 4, 2012

FLSA Pitfall to Avoid - Overtime and Wage Compliance at Online Event

December 6, 2012

Promoting and Advertising Dietary Supplements in Compliance with FDA and FTC Regulations at Hilton Salt Lake City Center

December 6, 2012

Establishing a Service Level Agreement (SLA) Process at Online Event

December 6, 2012

NLRB Effects on Social Media, Non-Union Employers and Other Changes at Online Event

December 6, 2012

International Trade Finance Payment Methods at Online Event

December 6, 2012

How to Write a Safety Plan that Complies with OSHA Requirements: Evacuation, Fire, Hazard Communication and Others at Online Event

December 6, 2012

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

December 6, 2012

Laboratory Inspection Readiness – Implementing GMPS for the Pharmaceutical Laboratory at Online Event

December 11, 2012

The Fundamentals of Accounts Receivable Collection Techniques at Online event

December 11, 2012

Deviations: What are they? Do you need to report? 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

Computerized System Validation - A Detailed Insight at Online event

December 12, 2012

Selection and Use of (Certified) Reference Material in Analytical Laboratories 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

Reducing eDiscovery risk for Pharmaceutical Companies at Online event

December 14, 2012

Food Recalls - Planning and conducting a Food Recall and Crisis Communication at Online Event

December 14, 2012

Food Recalls - Planning and conducting a Food Recall and Crisis Communication at Online Event

December 14, 2012

HITECH Changes to HIPAA at Online Event

December 19, 2012

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

December 21, 2012

FDA Enforcement and Your Compliance Program at Online Event

December 21, 2012

Trade Compliance Automation – Export Documentation & Electronic Information Filing at Online Event

December 21, 2012

FDA Enforcement and Your Compliance Program at Online Event

January 4, 2013

Using The Legal Guideposts to Create Social Media Success (for Healthcare/Lifescience Companies) at Online Event

January 6, 2013

How to Obtain a Canadian Medical Device License at Online event

January 7, 2013

Information Security Policy Development Dos and Don’ts at Online Event

January 8, 2013

Procurement Cards (P-Cards) - Fraud Detection, Prevention, and Deterrence at Online Event

January 9, 2013

Integrating COBIT with COSO and Other Frameworks at Online Event

January 9, 2013

Sampling Plans for (FDA) Quality Audits at Online event

January 9, 2013

The application of Lean Six Sigma methodology for U.S. FDA-Regulated Industries at Online Event

January 10, 2013

Gluten-Free Labeling Under the Current FALCPA of 2004 and Beyond at Online Event

January 11, 2013

Translating ERM Concepts into Something Your Organization Can Understand at Online Event

January 11, 2013

Mitigating the Risk of Wage Claims: Workers misclassification and IRS Audit at Online Event

January 11, 2013

Pharma and Biopharma Quality System Refresher Course 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 14, 2013

Webinar on Supply Chain Finance at Online Event

January 14, 2013

Essentials of Sterilizing Grade Filter Validation at Online event

January 15, 2013

OSHA Process Safety Management (PSM) Compliance Directive (CPL) and Interpretations at Online Event

January 15, 2013

Optimal Clinical Supply Planning for Global Drug Development at Online event

January 15, 2013

Fraud in Social Media and How to Protect Yourself and Your Organization at Online Event

January 15, 2013

OSHA Process Safety Management (PSM) Compliance Directive (CPL) and Interpretations at Online Event

January 15, 2013

Effective Discipline and Lawsuit-Proof Termination at Online Event

January 15, 2013

Why and How to Go Global - 5 Foreign Market Entry Techniques at Online Event

January 17, 2013

Understanding FDA and Avoiding Inspections Leading to Warning Letters, Seizures, Injunctions and Prosecutions at Hilton San Francisco Fisherman's Wharf

January 17, 2013

Allergen Awareness and Control in Food Processing at Online Event

January 17, 2013

How to Avoid Protocol Deviations at Development and Execution Phase of a Global Clinical Trial at Online Event

January 17, 2013

One and a Half-day In-person Seminar: “Effective Complaint Handling, Medical Device Reporting and Recalls -- Avoiding Costly Errors” at San Diego, California

January 17, 2013

Food Safety: After Disaster Strikes at Online Event

January 17, 2013

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

January 18, 2013

Make your Electronic Health Records HIPAA Compliant at Online Event

January 18, 2013

Effective OSHA Auditing - Creating Audit Documents for a Successful OSHA Audit at Online Event

January 18, 2013

Clinical Trial Quality and Risk Management - A Detailed Guide To Be Compliant and Manage Risks at Online Event

January 21, 2013

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

January 22, 2013

Regulation of Advanced Therapy Medicinal Products in Europe at Online Event

January 22, 2013

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

January 22, 2013

Implementing Performance Metrics for Clinical Research Associates (CRAs) and Data Targeted Monitoring at Online Event

January 23, 2013

Microbiological Sampling of Foods at Online Event

January 23, 2013

Auditor Independence: Challenges and Opportunities 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 23, 2013

Drug Marketing Launch - Framework for a Pharmaceutical Product Marketing Launch at Online Event

January 23, 2013

29 CFR 1910.147 | OSHA Hazardous Energy Control Standards at Online Event

January 23, 2013

Internal Auditor Independence and Objectivity - Challenges and Opportunities at Online Event

January 24, 2013

Compliance Processes for Life Science Products in Brazil, Russia, India, China markets at Sheraton San Diego Hotel and Marina

January 24, 2013

Third Party Information Security Assessment at Online Event

January 24, 2013

Statistical Considerations for ICH Guidelines at Sheraton San Diego Hotel and Marina

January 24, 2013

Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices at Grand Hyatt San Francisco

January 24, 2013

cGMP: Strategies for implementation and compliance for Phase I Investigational Drug and Biologic products at Online Event

January 24, 2013

Medical Device Risk Management A to Z - Best Practices for Effectiveness and Efficiency at Grand Hyatt San Francisco

January 24, 2013

Objectionable Microorganisms in an Aseptic Environment at Online Event

January 24, 2013

Practical techniques to help senior management and boards oversee management’s risk appetite and tolerance at Online Event

January 24, 2013

3-hr Virtual Seminar: OSHA Compliance Strategies for Auditing and Training Programs at Online Event

January 25, 2013

Basic Cell Culture & Fermentation - Process Development & Manufacture at Online Event

January 25, 2013

Informed Consent - A Process, Not a Piece of Paper at Online Event

January 25, 2013

CDISC - FDA’s Expectations, Requirements For US FDA Submissions, Concepts And Implementation at Online Event

January 28, 2013

HIPAA Risk Analysis: The HIPAA Standard, HIPAA Security rule at Online Event

January 28, 2013

Lockout/Tagout of energy (OSHA Regulation 29 CFR 1910.147) at Online Event

January 28, 2013

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

January 29, 2013

Purchasing Card Compliance with IRS Guidelines - Credit Cards for Business Use at Online Event

January 29, 2013

Preparing for an Office of Civil Rights (OCR) Audit at Online Event

January 29, 2013

Particulates in Biological products. Why test them and what are the new reporting requirements at Online Event

January 29, 2013

2013 Mandatory Food Safety Control Guidance for Retail Establishment at Online Event

January 30, 2013

Learning how to comply with 1910.1030 Bloodborne Pathogens at Online Event

January 30, 2013

Promoting Business Continuity with Suppliers and Business Partners at Online Event

January 30, 2013

Directors and Officers (D&O) Liability and Insurance Training for Risk Managers at Online Event

January 30, 2013

The Customs-Trade Partnership against Terrorism (C-TPAT) Requirements Training at Online Event

January 31, 2013

CRO GCP Compliance Failure - What Are The Sponsors Options? at Online Event

January 31, 2013

Healthcare Medical Software/Applications - Risks, Validation & Interoperability at Grand Hyatt San Francisco

January 31, 2013

Introduction to Business Ethics - Maintaining Shareholder Value at Online Event

January 31, 2013

Auditing the Human Resource Function & Human Resource Metrics at Grand Hyatt San Francisco

January 31, 2013

Food Marketing Claims: Risks of Enforcement Actions and Class Action Lawsuits, Defense Strategies and Best Practices at Grand Hyatt San Francisco

January 31, 2013

Process Validation for Medical Devices - The Regulatory Approach at Online Event

January 31, 2013

Auditing the Human Resource Function - Seminar By ComplianceOnline at Grand Hyatt San Francisco

January 31, 2013

“Claiming to free from” An Approach to Validating Allergen Cleaning Procedures at Online Event

February 1, 2013

Taking the Risk and Complexity out of Business Continuity (for Healthcare Organizations) at Online Event

February 1, 2013

Human Resource Metrics - Seminar By ComplianceOnline at Grand Hyatt San Francisco

February 5, 2013

Medical Device Complaints, MDR’s and Recalls at Online Event

February 5, 2013

Regulatory Compliance for Food Supplements in the EU - Registration, Labeling, Acceptable Marketing Claims at Online Event

February 5, 2013

Affirmative Action and Recent Trends within the OFCCP at Online Event

February 5, 2013

Immunogenicity to biologics: processes, impact on efficacy and safety, and management strategy at Online Event

February 5, 2013

Common Misconceptions in OSHA Recordkeeping at Online Event

February 6, 2013

Investigator Initiated Trials - What Are We Doing to Ensure Human Subject Protection? at Online Event

February 6, 2013

Training on Current ICH GCP Guidelines at Online Event

February 6, 2013

(Medical Claim) Modifiers: Complying with Payer Variations at Online Event

February 7, 2013

One and a Half-day In-person Seminar: Drug Master Files (DMF) - Translating FDA Guidances into usable documentation at San Diego, California

February 7, 2013

2-day In-person Seminar: Why is FDA at my facility, and what do I do during an inspection? at San Diego, California

February 7, 2013

Drug Master Files (DMF) - Translating FDA Guidances into Usable Documentation at Sheraton San Diego Hotel and Marina

February 7, 2013

Effective Complaint Handling, Medical Device Reporting and Recalls -- Avoiding Costly Errors at Tampa International Airport

February 7, 2013

FDA’s GMP Expectations for Phase I and First-in-Man Clinical Trials at Sheraton San Diego Hotel and Marina

February 7, 2013

Computer System Validation - Reduce Costs and Avoid 483s at Courtyard Phoenix Camelback

February 7, 2013

2-day In-person Seminar: Computer System Validation - Reduce Costs and Avoid 483s at Scottsdale Studios

February 8, 2013

BYOD and Information Security - Is this an Oxymoron? at Online Event

February 11, 2013

Complying with the Rules & Regulations Pertaining to Letters of Credit at Online Event

February 11, 2013

HIPAA Privacy In 2013 and Beyond 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 11, 2013

Introduction to Biotechnology Analytical Methods at Online Event

February 12, 2013

Auditing for Microbiological Aspects of Pharmaceutical and Biopharmaceutical Manufacturing at Online Event

February 12, 2013

How to Build an Anti-Fraud Culture – Going BEYOND Just Ethics at Online Event

February 12, 2013

Why and How - Verification of Compendial Methods - USP at Online Event

February 12, 2013

Effectiveness Measures in CAPA and Risk Management Plans: Applying LSS for Quality Metrics at Online

February 12, 2013

Foreign Material Control in Food Processing at Online Event

February 13, 2013

The Role of the Board in Oversight of Enterprise Risk at Online Event

February 13, 2013

How to prepare for an OCR/HHS HIPAA/HITECH audit at Online Event

February 15, 2013

The Psychology and Law of Workplace Misconduct: From the Manipulative to the mentally ill at Online Event worldwide

February 18, 2013

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

February 18, 2013

Roles and Responsibilities of HR professionals at Online Event

February 19, 2013

Accounts Receivable - Fraud Detection, Prevention, and Deterrence at Online Event

February 20, 2013

HIPAA Security Rule Compliance - Risk Analysis and Documentation are Keys to Compliance at Online

February 20, 2013

How to Develop an Export Compliance Manual at Online Event

February 20, 2013

Marketing Compliance for Pharma Management at Online Event

February 20, 2013

How to Investigate Malpractice Insurance Risk - Personal Liability, Errors and Omissions at Online Event

February 20, 2013

Auditing Technology and IT Investment Management 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

February 20, 2013

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

February 20, 2013

HIPAA Security Rule Compliance - Risk Analysis and Documentation are Keys to Compliance at Online Event

February 21, 2013

Basic Statistics for Microbiological Sampling at Online Event

February 21, 2013

IPPF Internal Audit Standard 2120: Assessing the Effectiveness of Risk Management Processes at Online Event

February 21, 2013

Cloud Computing Compliance, Protected Data Usage in Cloud, Legal and Compliance Challenges at Online Event

February 21, 2013

“There is always one piece left over” Managing Food Safety and Hygiene Issues relating to Engineers and Service Contractors at Online Event

February 22, 2013

Managing PHI Breach - Office of Civil Rights Incident and Mitigation Requirements for Protected Health Information at Online Event

February 26, 2013

Clinical Laboratory Incident Management Plan - GLP and FDA Compliance at Online Event

February 26, 2013

Workable HACCP: Developing and Implementing an Integrated Food Safety Management for Food Businesses at Online Event

February 26, 2013

Trends in Audit, Risk, and Compliance: Integrating your “ARC” at Online Event

February 27, 2013

Doing Competitive Intelligence Yourself –How to add CI to your personal corporate toolbox at Online Event

February 28, 2013

Introduction to Risk and Control Matrices for Internal Audit/SOX/Assurance at Online Event

February 28, 2013

Reducing Clinical Practice Variance in Value Driven Healthcare: Why Does it Matter? at Online Event

February 28, 2013

The Role of Social Media in Food and Drug Advertising and Regulatory Compliance Implications at Online Event

February 28, 2013

Auditing and Administrating Human Resource Policies and Practices at Online Event

March 1, 2013

Knowing Your Risk-Impact Quotient (for Healthcare Organizations) at Online Event

March 5, 2013

HIPAA Business Associates – 2013 New Requirements and Responsibilities for Compliance at Online Event

March 5, 2013

Designing Effective and Efficient Extractables/Leachables Studies for Biologics at Online Event

March 5, 2013

The Most Serious FDA 483s - How to Avoid Them at Online Event

March 5, 2013

Respirator Protection Program - 29 CFR 1910.134 at Online Event

March 5, 2013

Social Media and Marketing FDA Regulated Products at Online Event

March 5, 2013

The Psychology and Law of Workplace Misconduct: From the Manipulative to the Mentally ill at Online Event

March 5, 2013

Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results at Online Event

March 6, 2013

Engineering Change Management for Pharmaceutical Capital Projects at Online Event

March 6, 2013

Implementing a Whistle-Blower Program - Detecting and Preventing Fraud at Workplace at Online Event

March 7, 2013

Initiating a Recall of Baby Food Successfully at Online Event

March 7, 2013

You have a Sterility Failure or Bioburden Excursion - Now What? at Online Event

March 7, 2013

OSHA Blood Borne Pathogens at Online Event

March 7, 2013

Traceability and Recall in Food Processing at Online Event

March 8, 2013

FDA Warning Letters - Stop Fumbling your Response and Effectively Demonstrate Compliance at Online Event

March 8, 2013

Federal Sentencing Guidelines for Organizations (FSGO) Guidelines for your GRC System at Online Event

March 8, 2013

A Systematic Approach To Writing Effective Standard Operating Procedures (SOPs) at Online Event

March 8, 2013

Understanding Disinfectant Qualification Studies – How to avoid errors at Online Event

March 12, 2013

How to Think Like a Crook - Money Laundering Prevention at Online Event

March 12, 2013

Accounting Standard Best Practices for Payroll at Online Event

March 12, 2013

Complimentary Webinar: The Evolving Role of the Chief Information Security Officer at Online Event

March 13, 2013

Excel Spreadsheets; Develop and Validate for 21 CFR Part 11 Compliance at Online Event

March 13, 2013

Introduction to the US Department of Justice's New FCPA Guidance Document - Key Takeaways & Future Planning at Online Event

March 13, 2013

Introduction to the US Department of Justice's New FCPA Guidance Document - Key Takeaways & Future Planning at Online Event

March 13, 2013

Introduction to the US Department of Justice's New FCPA Guidance Document - Key Takeaways & Future Planning at Online Event

March 13, 2013

Social Media Compliance for Healthcare Organizations at Online Event

March 14, 2013

In-Plant Validation for Food Safety at Online Event

March 14, 2013

Dietary Supplement Claims and Labeling at Online Event

March 14, 2013

Electronic Records & Electronic Signatures; 21 CFR Part 11 at Online Event

March 14, 2013

What to Do to Establish a Compliant I-9 program at Online Event

March 14, 2013

Podiatry Coding and Billing at Online Event

March 14, 2013

System Based Inspections - Laboratory Controls at Online Event

March 14, 2013

Validation of Cleaning: An Essential Tool to Remove Food Allergens at Online Event

March 14, 2013

Transferring Medical Device Production to a Contract Manufacturer at Online Event

March 14, 2013

Finding Out The Truth in Investigatory Interviews: Falsehoods, Deceptions, Omissions and Interference at Online Event

March 14, 2013

Transferring Medical Device Production to a Contract Manufacturer - Decision Making Process and Procedures at Online Event

March 15, 2013

Effective OSHA Auditing - Creating your Own Document that Means Something to your Supervisors at Online Event

March 15, 2013

Worker Safety - How to Reduce Accidents and Injuries Caused by Human Error at Online Event

March 18, 2013

The Corporate Director's Fiduciary Role and Management's Relationship at Online Event

March 18, 2013

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

March 19, 2013

3-hr Virtual Seminar: Affirmative Action and the OFCCP - An In-depth Primer at Online Event

March 19, 2013

Writing Clinical Data Queries - Best Practices and Pitfalls at Online Event

March 19, 2013

Achieving Closed-loop CAPA - Meeting FDA Expectations at Online Event

March 20, 2013

Building an Effective Cost Management System with Activity Based Costing at Online Event

March 20, 2013

Competitive Intelligence Compliance Issues: Tools For Business Best Practices at Online Event

March 20, 2013

FDA's Import Requirements and Managing the Import of FDA Regulated Products: 2-day In-person Seminar at Boston Park Plaza Hotel & Towers

March 20, 2013

Best Practices in Document Approval, Control, and Distribution at Online Event

March 21, 2013

Procurement Cards Fraud | P-Cards – Fraud Detection and Prevention at Online Event

March 21, 2013

Medical Device Recall - FDA Authority, Policy and Best Practices to Avoid / Manage: 2-day In-person Seminar at DoubleTree Bloomington - Minneapolis South

March 21, 2013

Practical Tips for Human Resource Recordkeeping/ Documentation Professionals at Online Event

March 21, 2013

14 CFR Part 120 and 49 CFR Part 40 requirements for a Drug and Alcohol program at Online Event

March 21, 2013

21 CFR Part 11 Electronic Records: Electronic Signatures at Online Event

March 22, 2013

NAFTA Qualification Process for USA, Mexico and Canada at Online Event

March 22, 2013

Global Medical Device Reporting - A Comparison of Worldwide Regulations at Online Event

March 22, 2013

Telecommuting: Effective Policies, Practices, and Programs at Online Event

March 22, 2013

3-hr Virtual Seminar: Auditing the Human Resource Function at Online Event

March 22, 2013

How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant? at Online Event

March 22, 2013

Core Risk Skills for Auditors and Facilitators at Online Event

March 22, 2013

Writing and Implementing Statistical Analysis Plans (SAPs) - Domestic and International Guidance under ICH E9 at Online Event

March 22, 2013

Compliance with Title I of the Americans with Disabilities Act (ADA) for Employees with Traumatic Brain Injuries (TBI) 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

March 25, 2013

Dispelling the Myths About Clinical Standardization at Online Event

March 26, 2013

The Interface Between Medicare and Medicaid, Anti-kickback Statute (AKS), Stark II and the Federal Civil False Claims Act (FCA) at Online Event

March 26, 2013

E-Payments Compliance - Complying to Auditor’s Standards at Online Event

March 26, 2013

Microbiological Risk: Do I Really Need to Test Raw Materials for Microorganisms at Online Event

March 28, 2013

Forced Degradation Studies/ Biologics Stability Programs for Biopharmaceuticals at Online Event

March 28, 2013

Political Contributions and Prohibitions on the Municipal Securities Business at Online Event

March 28, 2013

Quality Practices for Research and Development (R&D) CMC Laboratories at Online Event

March 28, 2013

Raw Materials Risk Management in GMP Facilities: Avoiding GMP non-Compliance Due to Raw Material Issues at Online Event

March 28, 2013

PII and PHI Disclosure - So Many Forms, What Do They All Mean? at Online Event

March 28, 2013

Forced Degradation Studies/ Biologics Stability Programs for Biopharmaceuticals at Online Event

March 29, 2013

Bioanalytical Methods Validation at Online Event

March 29, 2013

Defining And Managing User Requirements For Computer System Validation at Online Event

March 29, 2013

Creating a Good Design History File (DHF) for Audit Success at Online Event

March 29, 2013

Food Marketing Claims in the United States: Regulatory and Litigation Risks, Defenses and Best Practices at Online Event

April 2, 2013

Emergency Response Preparedness: Creating a Plan That Works at Online Event

April 2, 2013

Medicare and Medicaid EHR Incentives for Eligible Professionals & Hospitals at Online Event

April 3, 2013

Medical Foods: Practical Tips to Meet FDA Requirements for Claims and Quality at Online Event

April 3, 2013

Effective Project Audit Implementation: Quality, Cost, Procurement Management at Online Event

April 3, 2013

Designing a Clinical Protocol for Vaccine Clinical Trial at Online Event

April 4, 2013

When is Corrective Action Not Enough - Doing and Documenting Corrections is an ISO 13485 Expectation at Online Event

April 4, 2013

Biosimilars Analytical Characterization and Comparability Studies: One and a Half-day In-person Seminar at The Courtyard Marriott San Diego Downtown

April 4, 2013

Credit Card Fraud Prevention and Detection at Online Event

April 4, 2013

3-hr Virtual Seminar: Annual ICH GCP Refresher Course at Online Registration

April 4, 2013

Which CSV Model Should you Use: V-model, GAMP 5 or ASTM E2500? at Online Event

April 4, 2013

Design of Experiments in Biotechnology Analytical Development at Online Event

April 4, 2013

Effective Environment Sampling - Designing and Implementing at Online Event

April 4, 2013

Dietary Supplement Adverse Event Reporting and Recordkeeping Requirements under the Dietary Supplement at Online Event

April 5, 2013

(Healthcare) Security Metrics: Selection and Interpretation at Online Event

April 9, 2013

3-hr Virtual Seminar: OSHA Recordkeeping Compliance at Online Event

April 9, 2013

Termination Pay: When To Pay It, How To Pay It And How To Tax It at Online Event

April 9, 2013

Complaint Handling in Compliance with FDA and ISO Regulations at Online Event

April 9, 2013

Focus on Internal Control - Is your Company Ready for the New COSO? at Online Event

April 9, 2013

Bank Secrecy Act (BSA) Audit Best Practices at Online Event

April 10, 2013

Auditing the QC Microbiology Laboratory for FDA Compliance at Online Event

April 10, 2013

Auditing the QC Microbiology Laboratory for FDA Compliance at Online Event

April 10, 2013

Preparing for a Centers for Medicare and Medicaid Services (CMS) Audit: What Not To Do at Online Event

April 10, 2013

Monitoring Impurities in Pharmaceutical Products - ICH Q3 requirements at Online Event

April 10, 2013

Auditing the QC Microbiology Laboratory for FDA Compliance at Online Event

April 10, 2013

Auditing the QC Microbiology Laboratory for FDA Compliance at Online Event

April 11, 2013

Best Practices for Conducting OOS Investigations (in Pharmaceutical Laboratories) at Online Event

April 11, 2013

Detecting and Preventing Financial Reporting Fraud at Online Event

April 11, 2013

How to Withstand an FDA Audit of your Facility at Online Event

April 12, 2013

Employees vs. Independent Contractors - Understanding Legal Differences and Staying Compliant at Online Event

April 12, 2013

Providing Assurance on GRC Activities at Online Event

April 12, 2013

The Control of Hazardous Energy (LOTO - Lockout/Tag-out) - OSHA 1910.147 at Online Event

April 12, 2013

Employees vs. Independent Contractors - Understanding Legal Differences and Staying Compliant at Online Event

April 12, 2013

Medical Devices: Designing and Implementing a Reimbursement Strategy Geared Toward CMS Reimbursement Approval at Online Event

April 12, 2013

Container Closure Systems for Liquid and Lyophilized Products at Online Event

April 12, 2013

Dietary Supplements Labeling - Avoiding Claims that Invite Scrutiny and Penalties at Online Event

April 12, 2013

How to Make GMP Training Fun and Engaging at Online Registration

April 15, 2013

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

April 15, 2013

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

April 15, 2013

Current Trends in Reporting Surgical Assistants at Online Event

April 16, 2013

Mobile Medical Applications: Software Regulatory Requirements at Online Event

April 16, 2013

Conventional Food Claims and Labeling at Online Event

April 17, 2013

California Wage and Hour Compliance: Payroll Unique to the Golden State! at Online Event

April 17, 2013

P2P Metrics and Reporting at Online Event

April 17, 2013

Why is FDA at my facility, and what do I do during an inspection?: 2-day In-person Seminar at Doubletree Chicago - Magnificent Mile

April 18, 2013

Using the ISP98 Model Forms for Standby Letters of Credit at Online Event

April 18, 2013

Statistics for GMP Auditors at Online Event

April 18, 2013

Laboratory Investigation Out-of-Specification Results at Online Event

April 19, 2013

Developing and Updating a “Compliant” Lab Compliance Plan (Medicare and Medicaid Focus) at Online Event

April 19, 2013

Developing and Updating a “Compliant” Lab Compliance Plan (Medicare and Medicaid Focus) at Online Event

April 19, 2013

Smoking and Curing Fish as a Food Preservative - Techniques and Methods at Online Event

April 19, 2013

Developing and Updating a “Compliant” Lab Compliance Plan (Medicare and Medicaid Focus) at Online Event

April 19, 2013

Developing and Updating a “Compliant” Lab Compliance Plan (Medicare and Medicaid Focus) at Online Event

April 19, 2013

Market and Sell an Over-the-Counter Drug Product in the United States 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 22, 2013

The New Combination Drug/Device Products CGMPs - Final Rule at Online Event

April 23, 2013

3-hr Virtual Seminar: Understanding Biofilm and Controlling It in Pharmaceutical Water Systems at Online Event

April 23, 2013

OSHA Process Safety Management (PSM) Compliance Directive (CPL) and Interpretations at Online Event

April 24, 2013

Social Media and Healthcare - Meeting Patient Needs and Desires, and Ensuring Privacy and Security at Online Event

April 25, 2013

Current Trends in Reporting Surgical Assistants at Online Event

April 25, 2013

Information Security Governance - Issues and Answers at Online Event

April 25, 2013

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

April 25, 2013

Information Security Governance - Issues and Answers at Online Event

April 25, 2013

Current Trends in Reporting Surgical Assistants at Online Event

April 25, 2013

Detecting and Preventing Internal and External Fraud: 2-day In-person Seminar at Renaissance Tampa International Plaza Hotel

April 25, 2013

Country of Origin Marking for U.S. Imports at Online Event

April 25, 2013

OSHA Inspections - Avoiding the 10 Most Common Mistakes at Online Event

April 25, 2013

The Sunshine Act Final Rule at Online Event

April 26, 2013

Food Recall Insurance: Companies in the United States' Food Supply Chain Should Pay Attention! at Online Event

April 26, 2013

Roadmap of California Medical Leaves: Ultimate Guide to PDL, FMLA, FEHA, SDI, CFRA, PFL, ADA and Workers Compensation at Online Event

April 26, 2013

FDA Regulatory Control of the Drug Development Process and Investigator Responsibility in the Process at Online Event

April 26, 2013

Acquisition Due Diligence for Global Trade Compliance at Online Event

April 27, 2013

Pre-conference Free Webinar - Risk Management and Business Process Mapping Skills at Online Event

April 30, 2013

BSA Training - Tips & Tools at Online Event

April 30, 2013

Internal Control in Sales, Accounts Receivable and Collections at Online Event

May 2, 2013

Design Controls - A Roadmap to Successful Implementation: One and a Half - day In-person Seminar at Courtyard Chicago Downtown/River North

May 2, 2013

The 510(k) Submission: Requirements, Contents, and Options at Online Event worldwide

May 2, 2013

Avoiding FDA 483 Observations by Identifying the Root Cause of Deviations at Online Event

May 2, 2013

Regulatory Requirements for IND to NDA, BLA and 505(b)(2) Applications at Online Event

June 19, 2013

Procure-to-Pay Fraud: Detecting and Preventing Purchasing, Receiving and Disbursement Frauds: 2-day In-person Seminar at Houston Marriott West Loop By The Galleria