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Event Conducting Reference Checks, Background Checks, and Alcohol and Drug Testing
Begins February 16, 2012
City Palo Alto
Country USA

Event HIPAA Privacy and Security Audits and Enforcement: What the new program is about, how it works
Begins February 17, 2012
City Palo Alto
Country USA

Event Submission Documentation for Sterilization Process Validation - Webinar By ComplianceOnline
Begins February 23, 2012
City Palo Alto
Country USA

Event Accelerating Bioassay Transfer in a GMP Environment - Webinar By ComplianceOnline
Begins February 23, 2012
City Palo Alto
Country USA

Event Navigating the Japan Regulatory and Clinical Trial Environment; Conducting Clinical Studies in Japan
Begins February 23, 2012
City Palo Alto
Country USA

Event FDA’s Current Thinking for Industry cGMPs for Phase 1 INDs
Begins February 24, 2012
City Palo Alto
Country USA

Event Device Master Record & Device History Record – requirements, contents and implementation - Webinar By ComplianceOnline
Begins February 29, 2012
City Palo Alto
Country USA

Event HIPAA Security Policies and Procedures: New finalized regulations bring new obligations
Begins March 2, 2012
City Palo Alto
Country USA

Event Managing Immunogenicity Risk in Biopharmaceuticals - Webinar By ComplianceOnline
Begins March 8, 2012
City Palo Alto
Country USA

Event Uniform Customs and Practice for Documentary Credits - Webinar By ComplianceOnline
Begins March 16, 2012
City Palo Alto
Country USA

Event Quality Agreements with Pharmaceutical/ Biologic Manufacturers and the Use of Drug Master Files
Begins March 30, 2012
City Palo Alto
Country USA

Event Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs --ComplianceOnline Medical Device Training
Begins April 5, 2012
City Palo Alto
Country USA

Event Risk Assessment-Compliance Using Easy To Fill Out Documentation
Begins September 18, 2012
City Palo Alto
Country USA

 

Past Events


Event Latin America – Understanding Regulatory Compliance Requirements Across Life Science Industry European Filing & Registration Procedures
Begins February 9, 2012
City Palo Alto
Country USA

Event Life Cycle Validation of GMP Potency Bioassays - Webinar By ComplianceOnline
Begins February 9, 2012
City Palo Alto
Country USA

Event Recruiting on a Limited Budget: Proven Low and No Cost Tools and Approaches
Begins February 9, 2012
City Palo Alto
Country USA

Event Medical Device Process Validation - Statistical Considerations
Begins February 8, 2012
City Palo Alto
Country USA

Event Prepare for Tougher U.S. FDA cGMP Compliance Audits - Webinar By ComplianceOnline
Begins February 7, 2012
City Palo Alto
Country USA

Event Full Day Virtual Seminar - Understanding Biofilm and Controlling It in Pharmaceutical Water Systems
Begins February 2, 2012
City Palo Alto
Country USA

Event Statistical Considerations for ICH Guidelines - Seminar By ComplianceOnline
Begins January 30, 2012
City Palo Alto
Country USA

Event Untangling the FMLA, ADAAA, GINA, and Workers Compensation Laws
Begins January 30, 2012
City Palo Alto
Country USA

Event Preparing for FDA GCP Inspections - Webinar By ComplianceOnline
Begins January 27, 2012
City Palo Alto
Country USA

Event Introduction to the Electronic Common Technical Document
Begins January 27, 2012
City Palo Alto
Country USA

Event Implementation of the USP GMP Potency Bioassay Suite - Webinar By ComplianceOnline
Begins January 26, 2012
City Palo Alto
Country USA

Event Telecommuting: Effective Policies, Practices, and Programs - Webinar By ComplianceOnline
Begins January 24, 2012
City Palo Alto
Country USA

Event New Dietary Ingredients in the Regulatory Scheme - Webinar By ComplianceOnline
Begins January 24, 2012
City Palo Alto
Country Albania

Event Application of CAPA in (Device) Sterilization – For the Non-Expert
Begins January 20, 2012
City Palo Alto
Country USA

Event SOPs for Clinical Trials – Regulatory Requirement and Key to Effective Management
Begins January 19, 2012
City Palo Alto
Country USA

Event Production and QMS Software Validation - An Excel Example
Begins January 18, 2012
City Palo Alto
Country USA

Event How to Format a Succinct and Comprehensive 510(k) Submission
Begins January 17, 2012
City Palo Alto
Country USA

Event 3-hr Virtual Seminar - IFRS: Financial Instruments
Begins January 16, 2012
City Palo Alto
Country USA

Event How Doctors of Chiropractic can Bill Medicare For Durable Medical Equipment and Stay Legally Compliant
Begins January 13, 2012
City Palo Alto
Country USA

Event EEO Update for Managers and Supervisors - Webinar By ComplianceOnline
Begins January 13, 2012
City Palo Alto
Country USA

Event Auditing the Human Resource Function - Webinar By ComplianceOnline
Begins January 12, 2012
City Palo Alto
Country USA

Event FDAs new enforcement initiative – Webinar By ComplianceOnline
Begins January 12, 2012
City Palo Alto
Country USA

Event Anticipated Changes to the EU Medical Device Directives; 2010 Changes and What the Future Holds for Licensees
Begins January 12, 2012
City Palo Alto
Country USA

Event Major CGMP Issues for 2012 - Webinar By ComplianceOnline
Begins January 10, 2012
City Palo Alto
Country USA

Event New Changes to the HIPAA Regulations - What’s about to go into effect and what else is on the way
Begins January 10, 2012
City Palo Alto
Country USA

Event FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program
Begins December 16, 2011
City Palo Alto
Country USA

Event Risk Management in (FDA) Quality and Manufacturing Areas – Understanding What the Regulators Expect and Working it to your Advantage
Begins December 15, 2011
City Palo Alto
Country USA

Event Complying with Legal Interviewing and Hiring - Webinar By ComplianceOnline
Begins December 15, 2011
City Palo Alto
Country USA

Event Dietary Supplements: Regulatory Compliance Requirements, Product Claims, Labeling Issues and FDA Updates
Begins December 14, 2011
City Palo Alto
Country USA

Event ISO 14644-1 - Risks and critical testing elements - Webinar By ComplianceOnline
Begins December 9, 2011
City Palo Alto
Country USA

Event Preventing Device Maintenance Related Recalls - Webinar By ComplianceOnline
Begins December 9, 2011
City Palo Alto
Country USA

Event Full-day Virtual Seminar - South Korea: Navigating the Regulatory and Clinical Trial Environment
Begins December 9, 2011
City Palo Alto
Country USA

Event Cats Paw Theory - The latest threat to employers and how to avoid it
Begins December 9, 2011
City Palo Alto
Country USA

Event Clinically-Related 483s and Warning Letters: Getting through the Maze
Begins December 8, 2011
City Palo Alto
Country USA

Event Draft Guidance for Device Industry and FDA - Postmarket Surveillance
Begins December 8, 2011
City Palo Alto
Country USA

Event Fundamentals of Clinical Research - Key players and roles for a successful and compliant research team
Begins December 6, 2011
City Palo Alto
Country USA

Event Incorporate FDAs New Process Validation Principles into Company Verification and Validation Planning
Begins December 6, 2011
City Palo Alto
Country USA

Event CAPA Details, Implementation and Q&A in Medical Device Setting
Begins December 5, 2011
City Palo Alto
Country USA

Event 5-hr Virtual Seminar: GMP Requirements for Combination Products for the Medical Products Industry
Begins December 5, 2011
City Palo Alto
Country USA

Event FDA Warning Letter - Webinar By ComplianceOnline
Begins December 2, 2011
City Palo Alto
Country USA

Event The GCP/ICH Obligations of Sponsors, Monitors, and Investigators - Barriers and Solutions
Begins December 1, 2011
City Palo Alto
Country USA

Event Validation of Bioanalytical Assays for Biologicals - Webinar By ComplianceOnline
Begins November 30, 2011
City Palo Alto
Country USA

Event Documentation and Discipline: Solutions to Successful Outcomes - Webinar By ComplianceOnline
Begins November 30, 2011
City Palo Alto
Country USA

Event Construction of the European Drug Master File (EDMF) for Regulatory Agencies
Begins November 18, 2011
City Palo Alto
Country USA

Event Do you have a GCP compliant Trial Auditing System/Process in place? - Risks & Rewards
Begins November 18, 2011
City Palo Alto
Country USA

Event Effective Preparation for Audits and Inspections in a Regulated Environment
Begins November 17, 2011
City Palo Alto
Country USA

Event Science-based (Software) Test Planning – Fewer Tests, Better Coverage
Begins November 17, 2011
City Palo Alto
Country USA

Event FDAs DDMAC Compliance: Current Issues and Emerging Perspectives - Webinar By ComplianceOnline
Begins November 17, 2011
City Palo Alto
Country USA

Event Going Global: Best Practices for Integrating Business Development and Regulatory Compliance
Begins November 16, 2011
City Palo Alto
Country USA

Event How to Document Employment Decisions Properly So It Will Stand Up in Court
Begins November 16, 2011
City Palo Alto
Country USA

Event The Future for Nano-materials in Food Contact Packaging - Webinar By ComplianceOnline
Begins November 15, 2011
City Palo Alto
Country USA

Event Workforce Planning Compliance, Ensuring your People can Maintain Performance with the Changing Demands
Begins November 15, 2011
City Palo Alto
Country USA

Event Critical Pharmaceutical Deviation Handling Practices - Establish a stringent deviation handling system
Begins November 15, 2011
City Palo Alto
Country USA

Event Failure Investigation and Root Cause Analysis - Simple Tools, Powerful Results
Begins November 15, 2011
City Palo Alto
Country USA

Event Successful Site Qualification Preparation Tools - Webinar By ComplianceOnline
Begins November 14, 2011
City Palo Alto
Country USA

Event Estimating Reliability Performance with Accelerated Life Tests
Begins November 11, 2011
City Palo Alto
Country USA

Event FDAs 2011 Draft Guidance on Financial Disclosure by Clinical Investigators
Begins November 11, 2011
City Palo Alto
Country USA

Event Medication Reconciliation and Post-Marketing Surveillance
Begins November 10, 2011
City Palo Alto
Country USA

Event Process Validation for Biological Products – Fitting PV into Process Development and QbD with New Regulations
Begins November 7, 2011
City Palo Alto
Country USA

Event 4-hr Virtual Seminar - Japan: Regulatory Compliance Requirements for Life Science Products
Begins November 4, 2011
City Palo Alto
Country USA

Event Durable Medical Equipment Revenue Program - Legal Compliance Program & Strategic Guidance
Begins November 4, 2011
City Palo Alto
Country USA

Event Effective Facility Management, Operations and Maintenance in a Regulated Environment
Begins November 3, 2011
City Palo Alto
Country USA

Event Why Pharmacovigilance (Phase IV Trials) will be increasingly seen: What do they tell us and why are they important?
Begins November 2, 2011
City Palo Alto
Country USA

Event How to prepare for and survive a CLIA inspection - Clinical Laboratories Improvement Act
Begins November 2, 2011
City Palo Alto
Country USA

Event 3-hr Virtual Seminar: Outsourcing Medical Device Software Development with Compliance to IEC 62304
Begins November 2, 2011
City Palo Alto
Country USA

Event FDA Warning Letter Closeout Program - Webinar By ComplianceOnline
Begins November 2, 2011
City Palo Alto
Country USA

Event The 2010 FDA warning letters: Revealing the critical conduct areas in clinical studies
Begins November 1, 2011
City Online Event,Palo Alto
Country USA

Event Critical Issues to Consider in Planning for and Providing Telemedicine Programs
Begins November 1, 2011
City Palo Alto
Country USA

Event Right-Sizing Requirements Elicitation: Balancing Lean, Sigma, and “Agile” Methods
Begins October 28, 2011
City Palo Alto
Country USA

Event GLP or GMP: A Comparison in Terms and Application for Drugs and Biologics - Webinar By ComplianceOnline
Begins October 27, 2011
City Palo Alto
Country USA

Event Corrective and Preventive Actions(CAPA) - 8 Steps to Achieve Compliance -- Medical Device Training
Begins October 26, 2011
City Palo Alto
Country USA

Event Reduce COTS Software Validation using the risk-based approach - Webinar By ComplianceOnline
Begins October 26, 2011
City Palo Alto
Country USA

Event Using an IQ / OQ / PQ Approach to Validating Medical Device Software
Begins October 26, 2011
City Palo Alto
Country USA

Event Microbiological Foodborne Threat- Risk mitigation and Crisis management
Begins October 25, 2011
City Palo Alto
Country USA

Event Medical Device Complaints, MDR’s and Recalls - Webinar By ComplianceOnline
Begins October 24, 2011
City Palo Alto
Country USA

Event Change Control Under the cGMPs and How the Regulations are Changing
Begins October 24, 2011
City Palo Alto
Country USA

Event 3-hr Virtual Seminar: Emerging FDA and EU Trends in IVD Regulatory Compliance
Begins October 21, 2011
City Palo Alto
Country USA

Event Addressing Impurities in Pharmaceutical Products - Webinar By ComplianceOnline
Begins October 20, 2011
City Palo Alto
Country USA

Event Compliance in Recruitment & Onboarding Strategies for Improved & Measureable Performance
Begins October 20, 2011
City Palo Alto
Country USA

Event Critical Compliance and Major Changes for the EU Clinical Trials Directive
Begins October 19, 2011
City Palo Alto
Country USA

Event How strong is your knowledge of GCP? A presentation on official GCP guidelines for compliant investigators and sponsors
Begins October 18, 2011
City Online Event,Palo Alto
Country USA

Event Closed-Loop CAPA - Meeting FDA Requirements - Webinar By ComplianceOnline
Begins October 18, 2011
City Palo Alto
Country USA

Event Understanding Hospitals Requirements of IEC 80001 and MDDS
Begins October 17, 2011
City Palo Alto
Country USA

Event Competitive Advantage of Linked Management Systems - Webinar By ComplianceOnline
Begins October 17, 2011
City Palo Alto
Country USA

Event Clinical Project Management - Webinar By ComplianceOnline
Begins October 14, 2011
City Palo Alto
Country USA

Event You have a sterility or Bioburden test failure - Now what? - Webinar By ComplianceOnline
Begins October 6, 2011
City Palo Alto
Country USA

Event Writing effective Risk Assessments to meet BRC Certification Requirements
Begins October 6, 2011
City Palo Alto
Country USA

Event Workplace Violence: Dealing with Insider Threat and Incidents of Workplace Revenge
Begins October 6, 2011
City Palo Alto
Country USA

Event Measuring your Human Capital – HR Metrics - Webinar By ComplianceOnline
Begins October 6, 2011
City Palo Alto
Country USA

Event How to Survive a DEA Inspection Series: DEA Due Diligence for Manufacturers and Distributors
Begins October 5, 2011
City Palo Alto
Country USA

Event Validation Basics A-Z: Planning, Implementing & Maintaining
Begins October 5, 2011
City Online Event,Palo Alto
Country USA

Event How to secure GCP compliance in Clinical Trials: The complete overview of the critical parameters --ComplianceOnline Clinical Training
Begins October 4, 2011
City Palo Alto
Country USA

Event Accounting of Disclosures under HIPAA: What the Rules Require Today and Whats Changed by the Proposed Rule
Begins October 4, 2011
City Palo Alto
Country USA

Event Hazardous Waste Regulation: 10 Major Differences Between Federal RCRA and California Hazardous Waste Regulations
Begins October 4, 2011
City Palo Alto
Country USA

Event Avoiding the Regulatory Pitfalls of Green Marketing Claims - Webinar By ComplianceOnline
Begins October 4, 2011
City Palo Alto
Country USA

Event The FDAs New Draft Guidance on Medical Device Change(s) and the 510(k)
Begins October 4, 2011
City Palo Alto
Country USA

Event Maintaining Food Safety and Customer Satisfaction through effective Specification Development and Implementation
Begins October 4, 2011
City Palo Alto
Country USA

Event Avoiding the 90 Percentage Syndrome: Why Software Project Status Reports are Often Wrong
Begins October 3, 2011
City Palo Alto
Country USA

Event An Introduction To The Food Safety Modernization Act (FSMA) - Webinar By ComplianceOnline
Begins September 30, 2011
City Palo Alto
Country USA

Event Power to the Patient: Managing Health Care Costs by Managing Demand - Webinar By ComplianceOnline
Begins September 30, 2011
City Online Event,Palo Alto
Country USA

Event Understanding Freezing, Annealing, Primary and Secondary Drying in the Freeze-Drying Process
Begins September 30, 2011
City Palo Alto
Country USA

Event Fault Tree Analysis: A Risk Management Tool - Webinar By ComplianceOnline
Begins September 30, 2011
City Palo Alto
Country USA

Event Back-Label Ingredient Statement for Personal Care Cosmetics: What, Why and How to INCI
Begins September 30, 2011
City Palo Alto
Country USA

Event How to transfer QC procedures for commercial products in pharma industry - ICH and USP guidelines - Pharma Webinar By ComplianceOnline
Begins September 29, 2011
City Palo Alto
Country USA

Event Pediatric Clinical Trials in the EU: Regulatory, Scientific, and Ethical Challenges
Begins September 28, 2011
City Palo Alto
Country USA

Event The CLIA Laboratory Inspection: Failure is not an Option
Begins September 28, 2011
City Palo Alto
Country USA

Event Analytical Method Lifecycle: From Design and Development through Validation and Transfer
Begins September 27, 2011
City Palo Alto
Country USA

Event California Wage and Hour Compliance: Payroll Unique to the Golden State!
Begins September 27, 2011
City Palo Alto
Country USA

Event Improving Sanitation Standard Operating Procedures In the Food Industry - Webinar By ComplianceOnlin
Begins September 27, 2011
City Palo Alto
Country USA

Event How to Identify Hazardous Wastes at the Work Place - Webinar By ComplianceOnline
Begins September 23, 2011
City Online Event,Palo Alto
Country USA

Event The Darker Side of Implementing Wellness Programs: Possible Career-Ending Decisions
Begins September 23, 2011
City Online Event,Palo Alto
Country USA

Event Nuts and Bolts of California Environmental Regulations – Differences between U.S. EPA and State Requirements
Begins September 22, 2011
City Palo Alto
Country USA

Event 21 CFR Part 11 Compliance; specifics needed to eliminate 483s - 21 CFR Part 11 Webinar By ComplianceOnline
Begins September 21, 2011
City Palo Alto
Country USA

Event Best Documentation Practices for FDA Compliance - Webinar By ComplianceOnline
Begins September 21, 2011
City Online Event,Palo Alto
Country USA

Event How to Survive a DEA Inspection Series: For Controlled Substances Manufacturers and Distributors
Begins September 20, 2011
City Palo Alto
Country USA

Event Design Control Project Management - Webinar By ComplianceOnline
Begins September 20, 2011
City Palo Alto
Country USA

Event Food Recalls - Planning and conducting a Food Recall and Crisis Communication --ComplianceOnline Food Safety Training
Begins September 20, 2011
City Palo Alto
Country USA

Event How to Design a Clinical Trial in the Target Therapies Era: New Endpoints
Begins September 20, 2011
City Palo Alto
Country USA

Event Beyond Incentives: How to Motivate Employees to Make Lifestyle Changes - Webinar By ComplianceOnline
Begins September 19, 2011
City Online Event,Palo Alto
Country USA

Event FDA Validation Requirements - Webinar By ComplianceOnline
Begins September 16, 2011
City Palo Alto
Country USA

Event Compliance in Executing Human Resource Policies and Practices - Webinar By ComplianceOnline
Begins September 16, 2011
City Palo Alto
Country USA

Event Eliminate the Confusion - New Requirements for Clinical Laboratories to Meet GCP
Begins September 15, 2011
City Palo Alto
Country USA

Event Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities - Pharma Webinar By ComplianceOnline
Begins September 15, 2011
City palo alto
Country USA

Event Tips for Every Importer: The Basics of Importing - Webinar By ComplianceOnline
Begins September 15, 2011
City Palo Alto
Country USA

Event A Rational Approach to Developing and Troubleshooting Dissolution Methods for a Variety of Purposes
Begins September 14, 2011
City Online Event,Palo Alto
Country USA

Event Full Day Virtual Seminar: Reliability Engineering Fundamentals for Medical Devices
Begins September 12, 2011
City Online Event,Palo Alto
Country USA

Event Why and How - Verification of Compendial Methods - USP
Begins September 9, 2011
City Palo Alto
Country USA

Event Does your pharmaceutical lab have GMP and non-GMP functions? - Laboratory Webinar
Begins September 8, 2011
City Palo Alto
Country USA

Event Eliminate the Confusion – Physician Quality Reporting System for Anesthesia Claims
Begins September 6, 2011
City Palo Alto
Country USA

Event Responding to FDA Form 483s and Warning Letters - Webinar By ComplianceOnline
Begins September 6, 2011
City Online Event,Palo Alto
Country USA

Event Webinar on How to Survive an I-9 Audit - Webinar By ComplianceOnline
Begins September 6, 2011
City Online Event,Palo Alto
Country USA

Event Why Nobody Believes the Numbers: The Secrets of Care Management Outcomes Measurement Revealed
Begins September 2, 2011
City Online Event,Palo Alto
Country USA

Event Container Closure Systems for Liquid and Lyophilized Products
Begins September 2, 2011
City Palo Alto
Country USA

Event Legal and Practical guidelines for Dealing with Psychiatric Disabilities at Work:
Begins September 1, 2011
City Palo Alto
Country USA

Event Common GCP Violations and Site Mistakes - How to Avoid them
Begins August 31, 2011
City Online Event,Palo Alto
Country USA

Event Auditing the QC Microbiology Laboratory for FDA Compliance - Webinar By ComplianceOnline
Begins August 31, 2011
City Palo Alto
Country USA

Event Risk Analysis Without Fear: Satisfying HIPAA & Meaningful Use Requirements for Privacy and Security
Begins August 30, 2011
City Palo Alto
Country USA

Event Common Misconceptions in OSHA Recordkeeping - Webinar By ComplianceOnline
Begins August 26, 2011
City Palo Alto
Country USA

Event How to Avoid the Environmental Compliance Nightmare - Webinar By ComplianceOnline
Begins August 26, 2011
City Online Event,Palo Alto
Country USA

Event Developing and Implementing an Effective Change control Procedure in the Pharmaceutical Laboratory
Begins August 25, 2011
City Palo Alto
Country USA

Event Drug accountability in clinical trials - Is your site GCP compliant?
Begins August 25, 2011
City Online Event,Palo Alto
Country USA

Event Preparing for an FDA Pre-Approval Inspection - Webinar By ComplianceOnline
Begins August 25, 2011
City Online Event,Palo Alto
Country USA

Event Little-Known Risks of Personnel Files - Webinar By ComplianceOnline
Begins August 24, 2011
City Palo Alto
Country USA

Event Predicting Product Life Using Reliability Analysis Methods - Webinar By ComplianceOnline
Begins August 19, 2011
City Palo Alto
Country USA

Event How Due Diligence in Accurate Adverse Event Reporting is the Key to a clean FDA Audit
Begins August 19, 2011
City Online Event,Palo Alto
Country USA

Event Virtual Seminar on Designing Medical Device Software to Prevent Product Recalls - Webinar By Complia
Begins August 19, 2011
City Palo Alto
Country USA

Event Sterilization Options for Challenging Products - Webinar By ComplianceOnline
Begins August 18, 2011
City Palo Alto
Country USA

Event Auditing Systems for 21 CFR Part 11 Compliance - Webinar By ComplianceOnline
Begins August 18, 2011
City Palo Alto
Country USA

Event Understanding the Difference: HIPAA Security Compliance Assessment v. HIPAA Security Risk Analysis
Begins August 18, 2011
City Palo Alto
Country USA

Event Strategies for implementation and compliance for Phase I Investigational Drug and Biologic products
Begins August 18, 2011
City Palo Alto
Country USA

Event Compliance Processes for Life Science Products - Webinar By ComplianceOnline
Begins August 17, 2011
City Palo Alto
Country USA

Event Verification of Compendial Methods - USP
Begins August 17, 2011
City Palo Alto
Country USA

Event ISO 13485 and medical device quality systems - practical strategies for planning, implementation and beyond
Begins August 17, 2011
City Online Event,Palo Alto
Country USA

Event Excel Spreadsheets; develop and validate for 21 CFR Part 11 compliance - Webinar By ComplianceOnline
Begins August 17, 2011
City Palo Alto
Country USA

Event Full Day Virtual Seminar : Annual GLP Refresher Course
Begins August 12, 2011
City Palo Alto
Country USA

Event Clinical Project Management - Webinar By ComplianceOnline
Begins August 12, 2011
City Online Event,Palo Alto
Country USA

Event Disinfectant Validation and Cleanroom Cleaning for all FDA and EMEA regulated companies - Webinar B
Begins August 12, 2011
City Palo Alto
Country USA

Event ITAR Compliance: A Guide to the International Traffic in Arms Regulations
Begins August 11, 2011
City Palo Alto
Country USA

Event Deviations, Investigations and CAPA - Webinar By ComplianceOnline
Begins August 11, 2011
City Palo Alto
Country USA

Event Are you a Compliant Principal Investigator? What you Must Know and Do to Ensure Trial Compliance
Begins August 11, 2011
City Online Event,Palo Alto
Country USA

Event Affirmative Action and the OFCCP: - Webinar By ComplianceOnline
Begins August 11, 2011
City Online Event,Palo Alto
Country USA

Event Design History Files, Device Master Records, Device History Records, and Technical Files / Design Dossiers - Webinar By ComplianceOnline
Begins August 9, 2011
City Palo Alto
Country USA

Event Review and Implementation of USP Analytical Instrument Qualification
Begins August 9, 2011
City Palo Alto
Country USA

Event How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant? - Webinar By ComplianceOnline
Begins August 9, 2011
City Palo Alto
Country USA

Event Vendor Qualification - Designing and Implementing an Efficient and Compliant Vendor Program
Begins August 8, 2011
City Palo Alto
Country USA

Event 360 Degree Approach to Health Information Privacy - Webinar By ComplianceOnline
Begins August 5, 2011
City Palo Alto
Country USA

Event Designing effective and efficient Extractables/leachables studies - Biotech Webinar By ComplianceOnline
Begins August 4, 2011
City Palo Alto
Country USA

Event FDA Requirements for Device Labeling: Development, Contents, Distribution, and Changes
Begins August 4, 2011
City Palo Alto
Country USA

Event Hidden Hazards in Writing Employee Handbooks - Webinar By ComplianceOnline
Begins August 3, 2011
City Online Event,Palo Alto
Country USA

Event Preparing for the UK Bribery Act - Webinar By ComplianceOnline
Begins August 2, 2011
City Online Event,Palo Alto
Country USA

Event Information Security and Payment Card Rules: Complying with PCI and HIPAA, and Protecting Patient Payment Data
Begins August 2, 2011
City Online Event,Palo Alto
Country USA

Event Full day Virtual Seminar on Pharmaceutical Stability - Webinar By ComplianceOnline
Begins July 29, 2011
City Palo Alto
Country USA

Event Learning from Recent FDA Warning Letters Related to Computer Validation and Part 11
Begins July 29, 2011
City Palo Alto
Country USA

Event How to manage an EPA inspection - Webinar By ComplianceOnline
Begins July 29, 2011
City Online Event,Palo Alto
Country USA

Event Vendor Qualification Auditing for FDA Computer System Compliance
Begins July 28, 2011
City Palo Alto
Country USA

Event Clinical Trial auditing - Identifying risks and building a more compliant and successful trial
Begins July 28, 2011
City Palo Alto
Country USA

Event Clinical Document Management and Collaborative Electronic Data Exchange in Clinical Trials - Webinar By ComplianceOnline
Begins July 28, 2011
City Palo Alto
Country USA

Event Advertising and Promoting FDA Regulated Products - Webinar By ComplianceOnline
Begins July 27, 2011
City Palo Alto
Country USA

Event The Investigational Medicinal Product Dossier (IMPD): EUs CTA vs. FDAs IND
Begins July 27, 2011
City Palo Alto
Country USA

Event IND Applications for the US FDA - Webinar By ComplianceOnline
Begins July 27, 2011
City Palo Alto
Country USA

Event Medical Device Change(s) and 510(k) Submissions - Webinar By ComplianceOnline
Begins July 26, 2011
City Palo Alto
Country USA

Event Wage and Hour Law: Complying with Federal, State and Local Regulations
Begins July 26, 2011
City Palo Alto
Country USA

Event Cal/OSHA Enforcement and Defenses – Recent Changes in the Law
Begins July 26, 2011
City Palo Alto
Country USA

Event US, EU and Japan GMP Requirements: Practical ICH Area Differences, Healthcare Authority Inspection Focus
Begins July 26, 2011
City Palo Alto
Country USA

Event Document Approval, Control, and Distribution: How to Meet FDA QSR and ISO 13485 Requirements
Begins July 22, 2011
City Palo Alto
Country USA

Event Full Day Virtual Seminar - US, EU and Japan GMP Requirements
Begins July 22, 2011
City Palo Alto
Country USA

Event Using the USP Effectively - Webinar By ComplianceOnline
Begins July 21, 2011
City Palo Alto
Country USA


 

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