Upcoming Events
- March 4 - 4, 2020 - Clinical Quality Management Systems (QMS): Establishing A Practical & Compliant Program
- March 10 - 10, 2020 - Responding to Clinical Observations: Developing Robust Audit & Inspection CAPAs
- March 11 - 11, 2020 - Cleanroom Microbiology – A Foundational Introduction
- March 12 - 12, 2020 - Regulatory GCP Inspections: Preparation, Participation & Follow-up
- March 16, 2020 - Statistical Hypothesis Tests: Concepts & Applications
Events By Month
Click on a month below to view its associated events.
March 2020 [+] (18 total)
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Clinical Quality Management Systems (QMS): Establishing A Practical & Compliant Program
March 4 - 4, 2020
1pm-2:30pm EST, Online Training
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Responding to Clinical Observations: Developing Robust Audit & Inspection CAPAs
March 10 - 10, 2020
Online Training; 1:00 - 2:30 PM EST US
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Cleanroom Microbiology – A Foundational Introduction
March 11 - 11, 2020
1pm-2:30pm EST, Online Training
Read more... -
Regulatory GCP Inspections: Preparation, Participation & Follow-up
March 12 - 12, 2020
1pm-2:30pm EDT, Online Training
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Statistical Hypothesis Tests: Concepts & Applications
March 16, 2020
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Drug Substance Quality Risk Management: A Practical Approach to Identify Critical Quality Attributes and Critical Process Parameters
March 17 - 17, 2020
1pm-2:30pm EST, Online Training
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Confidence-Reliability Calculations and Statistically Valid Sample Sizes
March 18, 2020
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Stability Programs – Key Factors in Meeting FDA/ICH Expectations
March 18 - 18, 2020
1pm-2:30pm EST, Online Training
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Pharmaceutical Supply Chain Management
March 19, 2020
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Stability Programs - Key Factors in Meeting FDA/ICH Expectations
March 19 - 19, 2020
1pm-2:30pm EST, Online Training
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Surviving an FDA Good Laboratory Practices (GLP) Inspection – Critical Tips For Compliance
March 24 - 24, 2020
1pm-2:30pm EST, Online Training
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FDA REMS Inspection Guide: Audit Preparedness Best Practices
March 25 - 25, 2020
1pm-2:30pm EST, Online Training
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10 Ways to Improve Measurement Systems Assessments
March 30, 2020
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Computer System Validation (CSV) for FDA-Regulated Computers
March 30, 2020
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The Dietary Supplement cGMP rule (21 CFR part 111)
March 31, 2020
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Is it Method Verification or Validation, or Just Semantics
March 31, 2020
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Drug Master Files: Understanding and Meeting your Regulatory and Processing Responsibilities
March 31, 2020
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Design History File (Design History File), the Device Master Record (DMR) and the Device History Record (Device History Record) - Principles of Lean D
March 31, 2020
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April 2020 [+] (9 total)
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Metrology: Statistical Analysis of Measurement Uncertainty
April 1, 2020
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3-Hour Virtual Seminar on FDA's section 804 Drug and 801(d)(1)(B) Biologic Importation Programs
April 1, 2020
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Change Management System
April 7, 2020
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Implementing an Effective CAPA System
April 10, 2020
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FDA's Problem with Software Monsters
April 13, 2020
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Medical Device Recalls – Keys To Implementing A Successful Approach
April 14 - 14, 2020
1pm-2:30pm EST, Online Training
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Root Cause Analysis for CAPA
April 20, 2020
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Responsibility for Off-label Claims in Social Media
April 22, 2020
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GMP Expectations for Products Used in Early Phase IND Studies
April 23, 2020
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Writing Excellent SOPs
July 10, 2020
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August 2020 [+] (1 total)
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Cleanroom Guangzhou Exhibition 2020
August 16 - 18, 2020
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