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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