March
21 Mar 2019Applied Statistics with Emphasis on Verification, Validation, and Risk ManagementKingwood, TX
21 Mar 2019Human Error Reduction in GMP-Related EnvironmentsPalo Alto
21 Mar 2019Statistical Justification for Using Small Sample Sizes and only 3 Lots in Process or Product ValidatPalo Alto
21 Mar 2019Human Error Reduction in GMP Related EnvironmentsPalo Alto
21 Mar 2019E/M Auditing Essentials: Improve Documentation and Decrease Improper PaymentsPalo Alto
21 Mar 2019Chief Compliance Officer: What does it take to do the job? The Organization's and CCO's ResponsibiliPalo Alto
22 Mar 2019FDA Inspections - Do's and Don'ts 2019Fremont
22 Mar 2019Two-Hour Virtual Seminar: Learning the OSHA Recordkeeping AnalysisPalo Alto
22 Mar 2019Building Accountability on your Clinical TeamsFremont
22 Mar 2019Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical ManufacturingPalo Alto
22 Mar 2019Virtual Seminar: Learning the OSHA Recordkeeping AnalysisPalo Alto
25 Mar 201910th Annual Congress on Bioenergy and Biofuelsbucharest
25 Mar 2019Building a Compliance Programme in the Healthcare IndustryFremont
26 Mar 2019Process Challenge Device Development for EO SterilisationPalo Alto
26 Mar 2019Live Webinar on FDA Inspection Preparation Guide: Handling 483s and Warning LettersAurora
26 Mar 2019Process Challenge Device Development for EO SterilisationPalo Alto
26 Mar 2019The Identification and Quantitation of low-level compounds for Impurity and Degradation AnalysesPalo Alto
26 Mar 2019505(b)(2) NDAsPalo Alto
27 Mar 2019CDISC Mapping 2 - ODM, MindMaps and ReferencesPalo Alto
27 Mar 2019Writing Effective and compliant SOPsPalo Alto
27 Mar 2019Risk-Based Monitoring for GCP CompliancePalo Alto
27 Mar 2019Live Webinar on Issues in Calibrations and Accuracy in Method ValidationAurora
27 Mar 2019Writing Effective and Compliant SOPsPalo Alto
27 Mar 2019Risk-Based Monitoring for GCP CompliancePalo Alto
27 Mar 2019CDISC Mapping 2: ODM, MindMaps and ReferencesPalo Alto
27 Mar 2019Managed Care Contracts and the Case Management Leader: Leading Your Department to Improved ReimbursePalo Alto
27 Mar 2019Effective Records Management and Document Control for Medical DevicesPalo Alto
27 Mar 2019CMS Two Midnight RulePalo Alto
27 Mar 2019ICH Q7 FDA Guidance – Its Structure, History, Application and Writer's IntentPalo Alto
28 Mar 2019Don't be a Victim - Say No and have it HonoredFremont
28 Mar 2019Virtual Seminar -- Latin America: Understanding Regulatory Compliance RequirementsPalo Alto
28 Mar 2019Guideline to Aseptic Technique and Clean Room BehaviorPalo Alto
28 Mar 2019QbD Approach to Analytical Method Lifecycle: Design, Development, Validation and TransferPalo Alto
28 Mar 2019Anti-Dumping (AD) and Countervailing Duties (CVD)Palo Alto
29 Mar 2019Secure Medical Device ProcurementPalo Alto
29 Mar 2019How FDA Trains its Inspectors to Review CAPA, and Best Practices for Inspection PreparationPalo Alto
April
1 Apr 2019Compliance with the New ICH GCP Revision 2 AddendumFremont
1 Apr 2019Understanding and Implementing a Technology Transfer ProcessFremont
2 Apr 2019ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements?Palo Alto
2 Apr 2019ISO 14971:2012 - Does Your Current Risk Analysis Still Comply with Your CE Mark Requirements?Palo Alto
2 Apr 2019Diversity and Inclusion 101Fremont
2 Apr 2019ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements?Palo Alto
3 Apr 2019Challenging the Complexity of Title V Air Permitting: Best PracticesPalo Alto
3 Apr 2019Challenging the Complexity of Title V Air Permitting: Best PracticesPalo Alto
3 Apr 20195 Proven Foreign Market Entry TechniquesFremont
3 Apr 2019Challenging the Complexity of Title V Air Permitting: Best PracticesPalo Alto
3 Apr 201921 CFR Part 11 and Annex 11 Compliance; Specifics for Data Integrity with SaaS/CloudPalo Alto
3 Apr 2019FDA Part 820 Basics - Everything you need to know to get your start-up Company CompliancePalo Alto
4 Apr 2019An Update on Discharge Planning Rules and Regulations for 2019Palo Alto
4 Apr 2019Seminar on Tougher Import Rules for FDA Imports in 2019Arlington, VA
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