ComplianceOnline
Conferences on Law & Regulations (past events)

ComplianceOnline organizes international conferences, seminars, workshops and other events in various fields, including business, education, government, global issues, health, medicine, industry, lifestyle and science....

ComplianceOnline has a presence in more than 20 countries around the world, including, Australia, Austria, Bangladesh, Brazil, China, Ireland and Kuwait.

ComplianceOnline hosts events on a wide range of topics, such as Aerospace, Agriculture, Alternative medicine, Anaesthesiology, Architecture, Interior design, Artificial Intelligence (AI) and Banking, among others. The events are designed to provide a platform for professionals and others to exchange knowledge, network, discuss new developments in respective fields as well as showcase products and services to a targeted audience.

Related topics
Showing 389 conferences
FDA`s Medical Device Software Regulation Strategy
Jun 2023
The Veterinary Drug Approval Process and FDA Regulatory Oversight
Feb 2023
Change Control Best Practices - Avoiding Unintended Consequences of Changes
Jul 2022
ComplianceOnline Medical Device Summit
Aug 2021
FDA Audit, Quality Assurance Practices, Responsibilities and Expectations
Sep 2020
Managing Domestic and Foreign FDA Inspections and the COVID-19 Impact
Aug 2020
Investigational New Drug (IND) & Investigational Device Exemptions (IDE) Applications Preparation and Submission, and Conducting FDA Meetings
Jun 2020
Implementing a Bullet Proof Quality System for FDA Audit Success
Jun 2020
Critical Anti-Fraud Audits under Procurement and Accounts Payable
Jun 2020
FDA`s Ambitious Regulation of Social Media
Jun 2020
How to Conduct an ACH Risk Assessment and Develop an Effective ACH Risk Management Program
Jun 2020
FDA`s New Import Program for - Strict Precision
Mar 2020
Managing an Effective AML Compliance Program
Jan 2020
Contracted Services: Ensuring Compliance with the CMS Hospital CoP Standards, Joint Commission and DNV
Dec 2019
Managing Your FDA Inspection: Before, During and After
Nov 2019
Is the Concurrent Delay Defense Dead
Aug 2019
HIPAA Privacy Rule Compliance-Understanding New Rules and Responsibilities of Privacy Officer
Jul 2019
Workplace Unconscious Bias: Minimizing the Impact on Discrimination, Hiring, Promotions, and Retention
Jul 2019
SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations
Jul 2019
Payments Fraud: Detect & Prevent Check, ACH and P-Card Schemes
Jul 2019
Basics of Testing Associated with Sterilization Validation and Routine Processing
Jul 2019
HIPAA Breach Evaluation and Reporting - What Qualifies as a Reportable Breach and How to Report It
Jul 2019
Monitoring High Risk Transactions
Jun 2019
FDA`s Expectations from Supplier Management for GMP: Quality Agreements and More
Jun 2019
Bank Secrecy Act Reporting Expectations - CTRs and SARs
Jun 2019
BSA/AML Contextual Awareness of High Risk Customers
May 2019
Legal and Contractual Perspectives of Managing the Remote/Virtual Employee
May 2019
Supplier Quality Assurance Agreements: Why a General Supply Agreement Not Be Enough with Some Suppliers
May 2019
AML High-Risk Transactions and Correspondent Banking
May 2019
How to Conduct an Internal Audit to Avoid an External One
May 2019
Storm Water Pollution Prevention Plans (SWPPP)
May 2019
FDA Recalls - Before You Start, and After You Finish
May 2019
Statistical Techniques for Medical Device Manufacturers
May 2019
Texting and Mobile Devices in Healthcare - HIPAA and CMS Requirements for Security of PHI
May 2019
Label Claims for food, Probiotics and Cosmetic products in Brazilian Regulatory System
May 2019
How to Ensure Your Foreign Vendors are FDA Compliant: Conducting Vendor Audits, Monitoring, and Using Checklists
May 2019
Excel Spreadsheets: Develop and Validate for 21 CFR Part 11 Compliance
May 2019
Pricing Contractor Jobsite Overhead Delay Costs
Apr 2019
The Healthcare Quality Improvement Act: Achieving Immunity in Your Peer Review Process
Apr 2019
Red Flags and EDD for Non-Bank Financial Institutions
Apr 2019
Managing the Alert/Case Clearing Investigation Process - BSA/AML/OFAC Compliance
Apr 2019
FDA Regulations & New Legislation for Marketing Cosmetics in the U.S
Apr 2019
Harmonized Tariff Schedule Classification
Mar 2019
Risk Based Monitoring for GCP Compliance
Mar 2019
Anti-Kickback, Fraud, Stark, and Marketing - Where are the Landmines?
Mar 2019
Selection and Use of (Certified) Reference Material in Analytical Laboratories
Mar 2019
The Most Serious FDA 483s - How to Avoid Them
Mar 2019
CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacturers
Mar 2019
ACH 101 for Originators
Mar 2019
Form W-4 for : Best Practice and Compliance Requirements
Mar 2019
FDA Regulations for Environmental Monitoring (EM) Program
Mar 2019
Mortgage Servicing Compliance: Meeting Extensive New Regulatory Expectations
Feb 2019
Fair Hearings from A Hearing Officer`s Perspective
Feb 2019
New Crystalline Silica Requirements and Strategies
Feb 2019
Form 941 for : All You Need to Know
Feb 2019
Introduction to Root Cause Investigation for CAPA
Feb 2019
Surviving an FDA Sponsor Inspection - Training for Success
Feb 2019
What the US, Canada and Mexico Want from a New NAFTA
Feb 2019
Identity Issues in Banking - 26 Red Flags and More
Feb 2019
Compliance Risk Management in Medical Devices, Pharmaceuticals, and Combination Products
Feb 2019
SR Letter 11-7 - Supervisory Guidance on Model Risk Management
Feb 2019
The SEC`s New Whistleblower Rules: Implications for Your Company`s Compliance and Fraud Program
Feb 2019
Data Governance for Computer Systems Regulated by FDA
Jan 2019
FinCEN`s New CDD Rule - The New Prong of the AML
Jan 2019
Healthcare Privacy and Security Regulations: Satisfying HIPAA, GDPR, 42 CFR Part 2, FERPA, and State Laws Protecting Health Information
Jan 2019
How to Prepare for an FDA Inspections?
Jan 2019
AML Model Validation: A Critical Need in the New Regulatory Environment
Jan 2019
Medical Marijuana in the Workplace
Jan 2019
Strategies for Mitigating the Impact of China Tariffs
Jan 2019
Internal Controls - What Every Manager Needs to Know
Dec 2018
Resolving Construction Disputes Using Alternative Dispute Resolution
Dec 2018
Vendor and Supplier Qualification Program for FDA Regulated Industries
Dec 2018
Pacing Delay - The Practical Effect on Projects and Delay Claims
Dec 2018
The Life Cycle Approach to Cleaning Validation
Dec 2018
Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results
Dec 2018
How To Detect Fraud Using Excel
Dec 2018
Medical Records: Compliance with CMS Hospital CoPs and Proposed Changes
Nov 2018
Ensuring Integrity and Security of Laboratory Data
Nov 2018
Auditing and examining Travel and Entertainment Expenses: Expense Reimbursement Fraud
Oct 2018
Workplace Violence Prevention Programs Including Active Shooter Scenarios
Oct 2018
Powerful Closed-loop CAPA - Meeting FDA Expectations
Oct 2018
Recent FDA Auditing Practices and the Top 10 Most Common Cited GMP Deficiencies
Sep 2018
Microsoft Excel - Let`s Look Beyond the Look-Up
Aug 2018
ACH 101 for Originators: ACH Rules
Jul 2018
EHRs and Coding Errors - What Every Practice Should Know
Jul 2018
Sunshine Act Reporting: Clarification for Clinical Research
Jul 2018
Developing a Contractor Safety Program
Jul 2018
How to Make Sure Your Foreign Vendors are FDA Compliant and Stay that Way
Jul 2018
Patients Suing Under HIPAA
Jul 2018
Practical Risk Appetite and Risk Tolerance
Jul 2018
Best Practices for Sexual Harassment Internal Investigations
Jun 2018
Best in Class Wage and Hour Compliance: The Federal Labor Standards Act (FLSA)
Jun 2018
Overtime: California Style
Jun 2018
Trade Compliance Seminar - Harmonized Tariff Schedule/Schedule B and NAFTA Rules of Origin and Documentation
Jun 2018
Medicare`s New Market-Based Reimbursement System for Clinical Laboratory Testing: Tipping Point Ahead for U.S. Labs in
Jun 2018
US Expatriate Compensation Planning and Reporting Methodology
Jun 2018
Implementing Bank Secrecy Act (BSA), Audit & Best Practices
Jun 2018
Document Control and Change Control Process in GxP/GMP Environment
Jun 2018
How to prepare for a CBP Audit
Jun 2018
World Class Cyber Incident Response Plans: Strong Responses to Attacks
Jun 2018
Environmental Compliance and Safety Management Inspection and Audit Techniques
May 2018
Form W-2 for : All You Need to Know
May 2018
Export Documentation and Procedure
May 2018
Employee Retention Toolkit : Set the Stage to meet Employee Expectation - Module 2
May 2018
Unemployment Claims: How to Prepare for Unemployment Hearings
May 2018
Document Control and Change Control Process in GxP/GMP Environment
May 2018
Paying Health Care Providers for Quality and Value: Key Trends and Stark Law Considerations
May 2018
Employers Guide to HIPAA
May 2018
Health Product Marketing authorization in Brazil - Documentation, Approval Process, Labeling, Advertising and Post Market Vigilance
May 2018
New Hire Legal Requirements and Process
May 2018
Anti-Fraud Controls in Payroll: Prevent Before It`s Too Late
May 2018
I-9 and Immigration Enforcement Bootcamp: Employer Best Practices & Compliance
Oct 2017
The Regulations of OTC Drugs
Oct 2017
Navigating the Maze for Post-Market Compliance -- Complaint Handling, MDRs, Recalls and Proposed Guidance on FDA Risk Benefits
Oct 2017
How TGA, FDA & Other Regulatory Authorities Inspect Computerized Systems for Data Integrity
Oct 2017
Australian Regulatory Guidelines for Medical Devices (ARGMD): Government Reimbursement, Requirements, Fees and Turnaround Time to Product Approval
Oct 2017
The Development and Implementation of a Robust Food Safety, Defense and Quality Assurance System
Oct 2017
Pharmaceutical Quality Management System (GMP Requirements, ICH Guidance, QbD, and USFDA/EMA Regulations)
Oct 2017
FDA Scrutiny of Promotion and Advertising Practices
Sep 2017
The A to Z of Trade Compliance for a U.S. Entity
Sep 2017
ISO 13485, ISO 14971, Quality Document Management, and Risk Management for Medical Devices
Sep 2017
FDA`s Import Program for - New Pathways and Pitfalls
Sep 2017
How to prepare a 510(k) Notification and a Technical File for the CE Mark
Aug 2017
A Comprehensive View of FDA Regulations for Medical Devices
Jul 2017
Modern HIPAA Compliance - Managing Privacy, Security, and Breach Notification in a World of New Technologies, New Threats, and New Rules
Jul 2017
FDA`s Regulation of Regenerative Medicine including Stem Cell Treatments, Tissue Engineering and Gene Therapies
Jul 2017
Understanding the FDA`s Regulation of HCT/Ps and Successful Product Development Strategies
Jul 2017
Applying the FDA Food Safety Modernization Act (FSMA) to Your Organization: 2-day In-person Seminar
Jul 2017
FDA Requirements for the Pharmaceutical Industry: Inspection, OTC Drugs, IND/NDA/ANDA, eCTD and GMP Requirements
Jun 2017
Efficient Process Validation Strategies and Validation Master Plan (VMPs) for Medical Devices
May 2017
CGMP Quality Principles for the FDA Regulated Industries: 2-Day In-Person Seminar
Nov 2016
Supplier and Contractor Qualification and Control:
Oct 2016
Best Practices for SOP Development and Implementation for the FDA Regulated Industry
Oct 2016
Advertising and Promotion of Dietary Supplements
Oct 2016
FDA`s Regulation of Implantable and Wearable Sensors
Oct 2016
Implementing and Monitoring AML/CTF Programs: 2-Day Workshop
Sep 2016
21 CFR Part 11/Annex 11 compliance for software validation and SaaS
Sep 2016
Building a Vendor Qualification Program for FDA Regulated Industries
Aug 2016
Mastering Risk Based Internal Auditing (RBIA)
Aug 2016
FDA Compliance and Clinical Trial Computer System Validation
Aug 2016
FDA Scrutiny of Purchasing/Supplier Controls
Aug 2016
Data Integrity: FDA, WHO and EMA`s Requirements
Aug 2016
HIPAA - Time to get Serious
Jul 2016
How to Minimize FCPA Exposure and Conduct Comprehensive Internal Investigations
Jul 2016
Navigating through Maze of In-vitro Diagnostics (IVD) Regulations: A systematic approach from Regulatory Strategy to Regulatory Approvals in U.S./Europe/Canada
Jul 2016
Designing a Supplier Qualification Program
Jul 2016
Understanding and Implementing the Medical Device Directive: 2-Day In-person Seminar
Jun 2016
Building a Sustainable Validation Program from Top to Bottom
May 2016
Preventing and Detecting Fraud in your Procure to Pay (P2P) Process
Apr 2016
Creating Effective SOP for Regulatory Compliance
Jan 2016
Social Media Risks, Rules, Policies and Procedures: Best Practices to Minimize Risks, Manage Use and Maximize Legal and Regulatory Compliance
Jan 2016
Bulletproof Workplace Investigations
Jan 2016
Process Robustness: The New FDA Paradigm
Jan 2016
Establishing a Service Level Agreement (SLA) Process
Jan 2016
Exempt v. Nonexempt: Ensuring Proper Classification of Employees for Compliance with Federal Overtime Laws
Dec 2015
Changing Trend in Risk Allocation - Differing Site Conditions
Dec 2015
Banking and Marijuana: When Federal and State Laws Collide
Nov 2015
Confined Space Rules for Construction that are in the Final OSHA Rule
Nov 2015
Building a Vendor Qualification Program for FDA Regulated Industries
Nov 2015
Computer System Validation - Reduce Costs and Avoid 483
Oct 2015
Computer System Validation - Reduce Costs and Avoid 483
Oct 2015
Complying with SSA and IRS Rules for Correcting Forms W-2 and 941
Oct 2015
The Logistics and Law of Exporting from the United States
Sep 2015
OSHA 10 Hour Course
Sep 2015
Fraud 101 for Compliance Professionals: Current Compliance Policies and Procedures
Sep 2015
CLOs - Analysis of Lenders
Sep 2015
Creating a Global Regulatory Plan
Aug 2015
Trends in Audit, Risk, and Compliance: Integrating your “ARC”
Aug 2015
Failure Mode and Effects Analysis for Design Improvement and Design Control
Aug 2015
Understanding FDA Regulations and Role in Opioid Pain Management
Aug 2015
CDOI, 790.03(h): The California Fair Claims Settlement Practices Regulations
Aug 2015
Understanding the Mobile Medical Applications Guidance
Aug 2015
Top 10 Contract Killer Clauses: How to Negotiate Out of Them
Jul 2015
Navigating the New FDA Draft Guidance on ISO 10993: Biological Evaluation of Medical Devices
Jul 2015
OSHA Enforcement for Employers Using Temporary Workers
Jul 2015
Internal Investigations: The Role of Documents in the Investigation
Jul 2015
Technical and Regulatory Writing for FDA Regulated Industries
Jul 2015
CDOI: Compliance with the California SIU Regulations
Jul 2015
Business Frauds: Detection, Prevention and Controls
Jul 2015
A+ on Retaliation Claims Compliance: Deal with the problems In House rather than in the Court House
Jul 2015
Using Q-Submission to Most Effectively Prepare for an FDA 510(k) Submission
Jul 2015
Treasury Management - Liquidity, Interest Rate, Foreign Exchange and Capital Risk Management
Jun 2015
Travel Pay: Handling it Correctly
Jun 2015
A+ Compliance with Pregnant Employees and New Parents: Pregnancy at Work
Jun 2015
Set-Up of Insurer Bad Faith, Defence of Bad Faith Suits and `Reverse Bad Faith` Claims: Insurer vs. Policyholder Perspectives
Jun 2015
OSHA - 10 Major Differences between Federal OSHA and California OSHA Compliance and Enforcement
Jun 2015
How to Most Effectively Prepare for and Manage FDA Inspection: Best Practices
Jun 2015
Monitoring Plans: 10 Rules of Effective Writing of Monitoring Plans
May 2015
California Laws Regulating Employment Screening and Safe Hiring
May 2015
The Canadian Food Label
May 2015
CAPA, Failure Investigation and Root Cause Analysis - FDA Expectations
May 2015
Understanding the New Custom Device Exemption Guidance
May 2015
Health Canada`s Enforcement of the Regulatory Requirements for the Manufacture, Advertising and Sale of Foods and Beverages
Apr 2015
Foreign Corrupt Practices Act (FCPA) and International Anti-Bribery Course [Course -2]
Apr 2015
Foreign Corrupt Practices Act (FCPA) and International Anti-Bribery Course [Course-1]
Apr 2015
Global and FDA Regulation of Electronic Cigarettes
Apr 2015
Regulatory Compliance for Dietary Supplements in the US, EU and Canada
Apr 2015
UDI Implementation
Apr 2015
Private Placements and Red Flags to Look For
Apr 2015
Affordable Care Act New Tax Penalties: Impact on Individuals and Employers
Apr 2015
China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)
Apr 2015
Product Standards, Menthol and FDA`s Deeming Regulation
Mar 2015
Manufacturing and Marketing Cosmeceutical* and Homeopathic OTCs: Complying with FDA`s Rules for Drug Products that do not require FDA Pre-Approval
Mar 2015
How to Successfully Manage an FDA High Risk Inspection
Mar 2015
Application of Disinfectants and Sterilants to Control Microorganisms; FDA Endotoxin Test – Understanding the Latest Revision
Mar 2015
OSHA Inspections - Avoiding the 10 Most Common Mistakes
Mar 2015
Character of Reputation Risk: Risk or Just an Impact? Techniques for Effective Management.
Mar 2015
Deconstructing Warning Letters - Using Warning Letters to Illustrate the FDA and Health Canada CFRs
Mar 2015
How to Avoid an FDA Warning Letter with a Strong CAPA Program
Mar 2015
Labor and Employment Law Update
Mar 2015
Are Your Criminal Background Checks Legally Compliant?
Feb 2015
Ensuring Regulatory Compliance of Food Establishments
Feb 2015
Corporate Governance Law 101 for Top Management to Monitor Compliance
Feb 2015
Clinical Trial Liability Lawsuits
Feb 2015
21 CFR 11 Compliance for Excel Spreadsheet
Feb 2015
HIPAA Omnibus Update - Tracking Down the Details
Jan 2015
Nutrition Facts - NLEA and Beyond
Jan 2015
A Systematic Approach To Writing Effective Standard Operating Procedures (SOPs)
Jan 2015
Alternatives for Financing Export Sales
Jan 2015
New AML Schemes to Detect and Prevent Fraudulent Transactions
Jan 2015
GAMP 5 as applied to FDA software validation - strategies to avoid warning letters
Jan 2015
cGMPs Beyond 21 CFR 110
Dec 2014
Effective Discipline and Lawsuit-Proof Termination: How to Remedy Performance and Conduct Problems While Minimizing Your Legal Risks
Mar 2014
CBP’s Trade Transformation Initiatives
Nov 2013
The Sunshine Act - Have you seen the light?
Nov 2013
FDA vs. EU Inspections - How to Prepare and What are the Differences
Nov 2013
Thorough and Complete Investigations and Follow-up - A Current Regulatory Expectation
Oct 2013
Premarket Review of New and Modified Tobacco Products
Oct 2013
Federal Sentencing Guidelines for Organizations (FSGO) Guidelines for your GRC System
Oct 2013
Charging for Investigational Drugs: Current Application of 21 CFR Part 312 and the Expanded Access Rules
Oct 2013
Effective Discipline and Lawsuit-Proof Termination: How to Remedy Performance and Conduct Problems While Minimizing Your Legal Risks
Oct 2013
Child Support Garnishments: Withholding Procedures for
Oct 2013
Building an Effective Global Code of Conduct: The Eight Essential Elements of Successful Customization
Aug 2013
Coping with a Difficult Compliance Officer when Responding to a 483, Warning Letter, Import Alert or Recall
Aug 2013
Anti-Kickback, Stark Laws and Marketing
May 2013
FDA Warning Letter Closeout Program
May 2013
Promoting and Advertising Dietary Supplements in Compliance with FDA and FTC Regulations: One and a Half-day In-person Seminar
May 2013
Conducting Successful FDA Meetings to Negotiate Product Development and Approval: 2-day In-person Seminar
Apr 2013
Medical Device Labeling (In-Vitro Lab “Home Brew” off - Label Guidance & Enforcement): 2-day In-person Seminar
Apr 2013
Dietary Supplements - Regulatory Compliance Requirements, Product Claims, Labeling Issues and FDA Updates
Apr 2013
Dietary Supplements Labeling - Avoiding Claims that Invite Scrutiny and Penalties
Apr 2013
Providing Assurance on GRC Activities
Apr 2013
Focus on Internal Control - Is your Company Ready for the New COSO?
Apr 2013
Microbiological Risk: Do I Really Need to Test Raw Materials for Microorganisms
Mar 2013
Applying Risk Management to Your Organization: 2-day In-person Seminar
Mar 2013
The Corporate Director`s Fiduciary Role and Management`s Relationship
Mar 2013
Obtaining Faster FDA 510(k) Approvals - The 510(k) as an Advocacy Document: One and a Half-day In-person Seminar
Mar 2013
Introduction to the US Department of Justice`s New FCPA Guidance Document - Key Takeaways & Future Planning
Mar 2013
FDA Warning Letters - Stop Fumbling your Response and Effectively Demonstrate Compliance
Mar 2013
Defining Computer System Validation & Software Development Life-Cycle
Feb 2013
IPPF Internal Audit Standard 2120: Assessing the Effectiveness of Risk Management Processes
Feb 2013
14 CFR Part 21, Subpart K Requirements for Parts Manufacturer Approvals (PMA) - FAA Approval
Feb 2013
How to Develop an Export Compliance Manual
Feb 2013
Complying with the Rules & Regulations Pertaining to Letters of Credit
Feb 2013
Conformance of Design History Files for Mature Medical Products
Feb 2013
Directors and Officers (D&O) Liability and Insurance - Everything a New Risk Manager Needs to Know
Jan 2013
New Finalized HITECH Amendments to HIPAA - How Policies and Practices Must Be Changed
Jan 2013
Risk Status Oversight – New Risk Oversight Expectations and Financial Reporting Requirements
Jan 2013
Auditor Independence: Challenges and Opportunities
Jan 2013
SOX Compliance for Foreign-based Public Companies : Implementing US Corporate Governance and Internal Controls
Jan 2013
Trade Compliance Automation – Export Compliance Screening
Nov 2012
21 CFR Part 11 - Complete Manual for Compliance and Success
Nov 2012
OSHA Ergonomics Compliance - What Every Organization Needs to Know
Nov 2012
Confidential Information and Human Resources
Oct 2012
Documentation and Investigative Report Writing
Oct 2012
Harmonized Tariff Schedule and Schedule B
Oct 2012
Canada Documentation and Procedures
Oct 2012
(QMS) Competence and Training Requirements per FDA QSR and ISO 13485
Aug 2012
Strategies for Preparing and Submitting Successful Citizen Petitions and Suitability Petitions to FDA
Aug 2012
Site Challenges in Conducting Investigational Device Trials
Aug 2012
Preventing, Documenting, and Dealing with FMLA Abuse
Aug 2012
Maximizing ROI on Each Compliance Effort - Webinar By ComplianceOnline
Jul 2012
One and a Half-day In-person Seminar: FDA Compliant GLP for Nonclinical Studies - For Pharmaceutical and Medical Device Industries
Jul 2012
Strategic Selection and Development of Immunogenicity Binding Methods
Jul 2012
Auditing GRC Programs - Webinar By ComplianceOnline
Jul 2012
Changes to Good Pharmacovigilance Practices in the EU - Webinar By GlobalCompliancePanel
Jul 2012
What Every FDA Regulated Company Needs to Know About its FDA District Office
Jul 2012
FDA’s Regulation of Veterinary Regenerative Medicine
Jun 2012
Thriving on Risk – Risk Management for Century
Jun 2012
Lawful Hiring and Termination: Using Social Media as a Part in Decision Making
Jun 2012
Navigating the Japan and South Korean Regulatory Compliance and Clinical Trial Environment
Jun 2012
Service Level Agreements (SLAs) - Preparation Guidelines for Effective SLAs - Webinar By ComplianceOnline
Jun 2012
Election Year Legal and Compliance - Webinar By ComplianceOnline
May 2012
IT Risk Management – EU Laws and Regulations
May 2012
Equipment Calibration in FDA QSR – Regulations and Warning Letters
May 2012
Physician Payment Sunshine Act and State Sunshine Law Compliance. Are you Prepared for the New Federal Requirements and Existing State Requirements?
Apr 2012
Lean Project Management For U.S. FDA-Regulated Industries
Apr 2012
Complying with the EU Cookies Law Ecosystem
Apr 2012
Acceptance Activities in FDA QSR - Regulations and Warning Letters
Apr 2012
Good Documentation Practices for GXPs
Apr 2012
Making Risk-Benefit Decisions – Preparing for the New FDA Guidance Documents
Apr 2012
California Environmental Regulations – Differences Between Federal EPA and State Requirements
Apr 2012
Medical Device Risk Management Using ISO 14971
Mar 2012
Ethical Hotlines, Whistleblowers and Compliance with the EU Data Privacy Laws & Regulations
Mar 2012
Reduce the Risks of Foreign Material Contamination - A Manufacturer`s Guide in Creating a Foreign Material Control
Mar 2012
Webinar: When Do You Need a 510K?
Mar 2012
Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada
Mar 2012
Defending Against an OFAC Investigation
Feb 2012
Global Data Transfer Solutions – Complying with EU Laws & Regulations
Feb 2012
Clear as Mud: Obtaining & Marketing your 510(K) with Today`s FDA
Jan 2012
Importing into the United States in Compliance with U.S. Customs & Border Protection (CBP)
Jan 2012
Validation and use of Access Databases in FDA regulated environments
Jan 2012
Record Keeping for a (Food) Recall: Keeping Records to Minimize the Affect of a Recall
Jan 2012
New Dietary Ingredients in the Regulatory Scheme
Jan 2012
FDA’s New Food Safety Law - What does It mean for everyone in the Global Food Chain
Jan 2012
An Introduction to the FDA New Drug Approval Process
Jan 2012
Introduction to FDA Good Documentation Practices
Jan 2012
Social Networking: Legal Concerns for Employers in Employee Misbehavior & Conducting Background Checks
Jan 2012
Accounting of Disclosures under HIPAA: What the Rules Require Today and What`s Changed by the Proposed Rule
Dec 2011
How to Identify Hazardous Wastes at the Work Place - Webinar By ComplianceOnline
Sep 2011
The Darker Side of Implementing Wellness Programs: Possible Career-Ending Decisions
Sep 2011
A Guide to HACCP Validation and Verification for Food Manufacturers and Restaurants
Sep 2011
HIPAA Security Policies and Procedures: What you Need for Compliance
Sep 2011
FDA Validation Requirements - Webinar By ComplianceOnline
Sep 2011
Drug Master Files - Understanding and Meeting your Global Regulatory and Processing Responsibilities
Sep 2011
Regulation of printing inks on food contact packaging materials in the US & EU
Sep 2011
A Rational Approach to Developing and Troubleshooting Dissolution Methods for a Variety of Purposes
Sep 2011
Investigator responsibilities and Legal commitments in Drug and Device Clinical Research
Sep 2011
Reliability Engineering Fundamentals for Medical Devices - Webinar By ComplianceOnline
Sep 2011
Eliminate the Confusion – Physician Quality Reporting System for Anesthesia Claims
Sep 2011
Responding to FDA Form 483s and Warning Letters - Webinar By ComplianceOnline
Sep 2011
Why Nobody Believes the Numbers: The Secrets of Care Management Outcomes Measurement Revealed
Sep 2011
Common GCP Violations and Site Mistakes - How to Avoid them
Aug 2011
Risk Analysis Without Fear: Satisfying HIPAA & Meaningful Use Requirements for Privacy and Security
Aug 2011
Preparing for an FDA Pre-Approval Inspection - Webinar By ComplianceOnline
Aug 2011
Design Reviews for Efficiency and Efficacy - Webinar By ComplianceOnline
Aug 2011
Full Day Virtual Seminar: Predicting Product Life Using Reliability Analysis Methods
Aug 2011
How Due Diligence in Accurate Adverse Event Reporting is the Key to a clean FDA Audit
Aug 2011
Understanding the Difference: HIPAA Security Compliance Assessment v. HIPAA Security Risk Analysis
Aug 2011
Sterilization Options for Challenging Products - Webinar By ComplianceOnline
Aug 2011
ISO 13485 and medical device quality systems - practical strategies for planning, implementation and beyond
Aug 2011
Food Allergen Programs - Current Trends, Technologies and Risk Mitigation
Aug 2011
Clinical Project Management - Webinar By ComplianceOnline
Aug 2011
Review and Implementation of USP <1058> Analytical Instrument Qualification
Aug 2011
Design History Files, Device Master Records, Device History Records, and Technical Files / Design Dossiers
Aug 2011
Vendor Qualification - Designing and Implementing an Efficient and Compliant Vendor Program
Aug 2011
360 Degree Approach to Health Information Privacy - Webinar By ComplianceOnline
Aug 2011
Trial Master File for Research Sites: Can You Pass FDA Inspection?
Aug 2011
Auditing the QC Microbiology Laboratory for FDA Compliance - Webinar By ComplianceOnline
Aug 2011
Information Security and Payment Card Rules: Complying with PCI and HIPAA, and Protecting Patient Payment Data
Aug 2011
Bioanalytical Methods Validation - Webinar By ComplianceOnline
Aug 2011
Analytical Test Methods Validation: FDA, ICH and USP Requirements - Webinar By ComplianceOnline
Aug 2011
Full day Virtual Seminar on Pharmaceutical Stability - Webinar By ComplianceOnline
Jul 2011
How to manage an EPA inspection - Webinar By ComplianceOnline
Jul 2011
Vendor Qualification Auditing for FDA Computer System Compliance - Webinar By ComplianceOnline
Jul 2011
Clinical Document Management and Collaborative Electronic Data Exchange in Clinical Trials
Jul 2011
The Investigational Medicinal Product Dossier (IMPD): EU`s CTA vs. FDA`s IND
Jul 2011
Full-day Virtual Seminar: IND Applications for the US FDA
Jul 2011
Advertising and Promoting FDA Regulated Products - Webinar By ComplianceOnline
Jul 2011
How to Avoid the Environmental Compliance Nightmare - Webinar By ComplianceOnline
Jul 2011
Cal/OSHA Enforcement and Defenses – Recent Changes in the Law
Jul 2011
Document Approval, Control, and Distribution: How to Meet FDA QSR and ISO 13485 Requirements
Jul 2011
Using the USP Effectively - Webinar By ComplianceOnline
Jul 2011
How to Meet HIPAA-HITECH Encryption Requirements - Webinar By ComplianceOnline
Jul 2011
Key Concepts in OSHA Recordkeeping – 2.5 hrs comprehensive webinar
Jul 2011
Validation of Analytical Methods and Procedures - Webinar By ComplianceOnline
Jul 2011
Eliminate the Confusion - Compliance for Anesthesia Services
Jul 2011
Navigating the new FDA world of Combination Products
Jun 2011
Developing a Governance Risk Management and Compliance Strategy
Jun 2011
Avoiding `Failure to Investigate` - Observations by Conducting Effective Investigations
Apr 2011
The 510(k) Process and Risk Management
Apr 2011
FDA`s Revised 510(k) Premarket Notification Process
Apr 2011
Vendor/Supplier/CRO Compliance – Lessons Learned & Rules to Live By
Apr 2011
What Health Reform (and other Recent Changes) Means for Corporate Compliance
Mar 2011
International Terms 2010 Rules - ComplianceOnline Trade And Logistics Webinar
Mar 2011
Social Media in a Regulated Environment - ComplianceOnline Banking and Financial Training
Mar 2011
Internal Control for Smaller Entities - A Practical Cost - Effective Guide to Strengthening Internal Controls
Mar 2011
How to prepare for Increased OSHA penalties in
Feb 2011
Last changes in Canadian ethics regulations for clinical trial
Feb 2011
Foreign Corrupt Practices Act (FCPA) Webinar 2010
Feb 2011
Don`t RISK to ignore RISKS. Understanding ISO 14971
Feb 2011
Understanding and Implementing FDA’S 21 CFR Part 11
Feb 2011
Improve Your Audit Checklist - ComplianceOnline Quality Management Webinar
Feb 2011
Get Tough on Corrective Actions - ComplianceOnline Quality Management Webinar
Jan 2011
cGMP: Strategies for implementation and compliance for Phase I Investigational Drug and Biologic products
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The Auditee Bill of Rights - ComplianceOnline Quality Management Webinar
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HR Audits: A Critical Compliance Process - ComplianceOnline HR Webinar
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Preparing for a GSA Audit - ComplianceOnline GSA Webinar
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The Riskability Integration. – Integrating strategies and HR in EGRCM. Steps to leverage the impact of EGRCM mandates
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Accident Investigations and the Law – How to Find out what really happened - ComplianceOnline OSHA Webinar
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The multinational scopes of US and EU export controls and economic sanctions laws - ComplianceOnline Trade And Logistics Webinar
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Incoterms `Terms of Sale`
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Using Social Media in a FDA Compliant Manner
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ComplianceOnline Webinar - Estimating Greenhouse Gas Emissions; Determining Your Carbon Footprint
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CAPA for Manufacturing, Financial Service Companies: Get it Right the Time (Efficient Process)
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Current dynamics of the current regulatory framework and the bills under consideration by Congress
Sep 2010
Best Practices on Developing a Regulatory Framework to expand energy efficiency and renewable energy markets
Sep 2010
Product Risk Management - ISO 14971 and ICH Q9
Aug 2010
NERC Compliance for Energy and Utility Companies – a risk intelligent approach
Aug 2010

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