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Event HIPAA Breach Notification - Webinar By ComplianceOnline
Begins May 30, 2012
City Palo Alto
Country USA

Event Election Year Legal and Compliance 2012 - Webinar By ComplianceOnline
Begins May 30, 2012
City Palo Alto
Country USA

Event 21 CFR Part 11 compliance for Electronic Medical Records
Begins May 30, 2012
City Palo Alto
Country USA

Event Food Safety Documentation - Webinar By ComplianceOnline
Begins May 31, 2012
City Palo Alto
Country USA

Event GLP or GMP: A Comparison in Terms and Application for Drugs and Biologics - Webinar By ComplianceOnline
Begins May 31, 2012
City Palo Alto
Country USA

Event What Are the Current Tools and Best Techniques for (Clinical Trial) Audit/Inspection Preparedness?
Begins May 31, 2012
City Palo Alto
Country USA

Event Device Corrections and Removals - Webinar By ComplianceOnline
Begins June 1, 2012
City Palo Alto
Country USA

Event Affirmative Action and Recent Trends within the OFCCP - Webinar By ComplianceOnline
Begins June 2, 2012
City Palo Alto
Country USA

Event Service Level Agreements (SLAs) - Webinar By ComplianceOnline
Begins June 4, 2012
City Palo Alto
Country USA

Event CLIA (Clinical Laboratory Improvement Amendments) Guidelines on Quality Control and Quality Assessment - Webinar By ComplianceOnline
Begins June 7, 2012
City Palo Alto
Country USA

Event FDA Acceptance of non-US Clinical Trials
Begins June 7, 2012
City Palo Alto
Country USA

Event Analytical Method Qualification and Validation
Begins June 8, 2012
City Palo Alto
Country USA

Event Effective Good Clinical Practice in Drugs and Medical Devices
Begins June 11, 2012
City Palo Alto
Country USA

Event Promoting and Advertising Dietary Supplements in Compliance with FDA and FTC Regulations - Webinar By ComplianceOnline
Begins June 13, 2012
City Palo Alto
Country USA

Event Risk Evaluation and Mitigation Strategies - Webinar By ComplianceOnline
Begins June 14, 2012
City Palo Alto
Country USA

Event Auditing Systems for 21 CFR Part 11 Compliance: Preparing Yourself for Inspection
Begins June 14, 2012
City Palo Alto
Country USA

Event Issue Detection and Escalation in Clinical Trial Settings
Begins June 19, 2012
City Palo Alto
Country USA

Event Understanding and Implementing ISO 17025 - Webinar By ComplianceOnline
Begins June 20, 2012
City Palo Alto
Country USA

Event Acceptance Sampling by Variables Using Z1.9 - Webinar By ComplianceOnline
Begins June 22, 2012
City Palo Alto
Country USA

Event Research Sites FDA Inspection - Webinar By ComplianceOnline
Begins June 27, 2012
City Palo Alto
Country USA

Event Full Day Virtual Seminar: Understanding and Effectively Controlling Biofilm in Pharmaceutical Water Systems
Begins June 28, 2012
City Palo Alto
Country USA

Event Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs - Webinar By ComplianceOnline
Begins June 29, 2012
City Palo Alto
Country USA

Event Risk Management for Human Resources - Webinar By ComplianceOnline
Begins July 10, 2012
City Palo Alto
Country USA

Event Verification of Compendial Methods According to the Revised USP Chapter - Webinar By ComplianceOnline
Begins July 11, 2012
City Palo Alto
Country USA

Event GAMP® 5 as applied to FDA software validation - strategies to avoid warning letters
Begins July 11, 2012
City Palo Alto
Country USA

Event Identifying risks and building a more compliant and successful trial
Begins July 12, 2012
City Palo Alto
Country USA

Event HPLC Outside the Box: How to Think Like a Chromatographer - Webinar By ComplianceOnline
Begins July 20, 2012
City Palo Alto
Country USA

Event Spreadsheet Validation: Understanding and satisfying FDA requirements
Begins August 8, 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 Affirmative Action Compliance and Your Recruiting Strategy - Webinar By ComplianceOnline
Begins May 24, 2012
City Palo Alto
Country USA

Event Pre-Approval Statements and Representations by Pharmaceutical Manufacturers - Webinar By ComplianceOnline
Begins May 24, 2012
City Palo Alto
Country USA

Event An Overview of Risk Management and Risk Analysis Techniques in Clinical Trials
Begins May 24, 2012
City Palo Alto
Country USA

Event Medical Device Reporting (MDR), Recall, Reports of Corrections and Removals - Webinar By ComplianceOnline
Begins May 23, 2012
City Palo Alto
Country USA

Event OSHAs Update of Hazard Communication - Webinar By ComplianceOnline
Begins May 22, 2012
City Palo Alto
Country USA

Event Supplier Controls to Meet Tougher U.S. FDA Requirements - Webinar By ComplianceOnline
Begins May 22, 2012
City Palo Alto
Country USA

Event Food Safety Traceability Systems - Webinar By ComplianceOnline
Begins May 17, 2012
City Palo Alto
Country USA

Event Cosmetic Products - Webinar By ComplianceOnline
Begins May 16, 2012
City Palo Alto
Country USA

Event Verification of Compendial Methods - USP - Webinar By ComplianceOnline
Begins May 16, 2012
City Palo Alto
Country USA

Event FDA Concerns on Alarm Standards and Safety - Webinar By ComplianceOnline
Begins May 16, 2012
City Palo Alto
Country USA

Event Best Practices for Maintaining an IND and IDE Application with FDA
Begins May 16, 2012
City Palo Alto
Country USA

Event Statistics in Pharmaceutical Quality Control - Webinar By ComplianceOnline
Begins May 11, 2012
City Palo Alto
Country USA

Event Equipment Calibration in FDA QSR – Regulations and Warning Letters
Begins May 11, 2012
City Palo Alto
Country USA

Event Developing and Updating a “Compliant” Lab Compliance Plan (Medicare and Medicaid Focus) - Webinar By ComplianceOnline
Begins May 10, 2012
City Palo Alto
Country USA

Event Decoding CLIA (Clinical Laboratory Improvement Amendments) Regulations - Webinar By ComplianceOnline
Begins May 10, 2012
City Palo Alto
Country USA

Event HIPAA Security Issues - Webinar By ComplianceOnline
Begins May 10, 2012
City Palo Alto
Country USA

Event Pre-Formulation and Formulation Development of a Sound Bio Pharmaceutical Formulation that is cGMP Compliant
Begins May 10, 2012
City Palo Alto
Country USA

Event FDA Software Validation Self-Check – plan an effective Internal Audit program
Begins May 9, 2012
City Palo Alto
Country USA

Event The National Labor Relations Act - Not Just for Union Companies
Begins May 9, 2012
City Palo Alto
Country USA

Event Calibration and Qualification in Analytical Laboratories - Webinar By ComplianceOnline
Begins May 8, 2012
City Palo Alto
Country USA

Event Effective Chief Compliance Officers (CCO) or Chief Risk Officers (CRO) Function - Organization and Responsibilities - Webinar By ComplianceOnline
Begins May 7, 2012
City Palo Alto
Country USA

Event Managing Social Media Risks in the Workplace - Webinar By ComplianceOnline
Begins May 3, 2012
City Palo Alto
Country USA

Event The Hero of Manufacturing Contamination Control -- The Microbiology Lab
Begins April 26, 2012
City Palo Alto
Country USA

Event Lean Project Management For U.S. FDA-Regulated Industries
Begins April 24, 2012
City Palo Alto
Country USA

Event Full-day Virtual Seminar: Critical Factors and Complexities in Payroll 201
Begins April 23, 2012
City Palo Alto
Country USA

Event Is Food from Chain Safe? Complying with the New Perishable Food Import Requirements
Begins April 19, 2012
City Palo Alto
Country USA

Event Avoiding Discrimination When Recruiting With Social Media Tools
Begins April 16, 2012
City Palo Alto
Country USA

Event Acceptance Activities in FDA QSR – Regulations and Warning Letters
Begins April 13, 2012
City Palo Alto
Country USA

Event Pharmaceutical Water System Use & Monitoring - Webinar By ComplianceOnline
Begins April 13, 2012
City Palo Alto
Country USA

Event Third Party Audit and Certification for Food Manufacturers - Webinar By ComplianceOnline
Begins April 12, 2012
City Palo Alto
Country USA

Event Handling Supplemental Pay Under the FLSA - Webinar By ComplianceOnline
Begins April 11, 2012
City Palo Alto
Country USA

Event HR for Financial and Senior Management and CPAs: How to Reduce Risk and HR costs
Begins April 10, 2012
City Palo Alto
Country USA

Event Making Risk-Benefit Decisions – Preparing for the New FDA Guidance Documents
Begins April 6, 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 QbD Approach to Analytical Method Lifecycle: Design, Development, Validation, Transfer
Begins April 4, 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 FDAs Oversight of Mobile Medical Applications (apps) for Use on Smartphones and Similar Mobile Devices
Begins March 28, 2012
City Palo Alto
Country USA

Event Transportation of Food Products: Temperature Control Compliance and Vicarious Liability
Begins March 27, 2012
City Palo Alto
Country USA

Event The HR Practitioner’s Guide To Adverse Impact Analysis - Webinar By ComplianceOnline
Begins March 27, 2012
City Palo Alto
Country USA

Event HPLC Method Development and Validation - Webinar By ComplianceOnline
Begins March 27, 2012
City Palo Alto
Country USA

Event Medical Device Risk Management Using ISO 14971 - Webinar By ComplianceOnline
Begins March 23, 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 Managing Immunogenicity Risk in Biopharmaceuticals - Webinar By ComplianceOnline
Begins March 8, 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 Device Master Record & Device History Record – requirements, contents and implementation - Webinar By ComplianceOnline
Begins February 29, 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 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 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 Conducting Reference Checks, Background Checks, and Alcohol and Drug Testing
Begins February 16, 2012
City Palo Alto
Country USA

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


 

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