Lifecycle Approach to Analytical Methods with QbD Elements: Design, Development, Validation, Transfer
Category: Drugs and Chemicals (Pharma) , Quality and Safety , Supply Chain and Manufacturing , Life sciences QA/QC , Life Sciences , QA/QC

Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results
Category: Laboratory Compliance , Testing and Validation , Quality and Safety , Laboratory , Life Sciences

Laboratory Inspection Readiness - Implementing GMPs for the Pharmaceutical Laboratory
Category: Drugs and Chemicals (Pharma) , Laboratory Compliance , All FDA Regulated Industry , Quality and Safety , Audits & Inspections , Laboratory , GLP & Other Best practices , Microbiology Laboratory , Drugs Regulations , Biotech Regulations , Audit & Inspection-Role , Lab Audit , Life sciences QA/QC , Best Practices & GXPs , Life Sciences , Regulatory Affairs , Common FDA Regulations , QA/QC

USP Hot Topics: What's Hot Now and How to Track Coming Changes and Influence USP
Category: Drugs and Chemicals (Pharma) , Laboratory Compliance , Laboratory Compliance , Quality and Safety , Audits & Inspections , Laboratory , Drug Development , Drugs Regulations , Audit & Inspection-Role , Lab Audit , Drugs Inspections , Life sciences QA/QC , Research & Development , Drug R & D , Regulations & Guidances , Life Sciences , Regulatory Affairs , QA/QC

QbD Approach to Analytical Method Lifecycle: Design, Development, Validation and Transfer
Category: Drugs and Chemicals (Pharma) , Biotechnology , Laboratory Compliance , GXP Pharmaceutical , Testing and Validation , Documentation and IT , Quality and Safety , Laboratory , Quality & Safety , Technologies and Processes , Drugs Regulations , Biotech Regulations , Documentation and Policy Management , Lifescience process & Procedures , Life sciences QA/QC , Regulations & Guidances , Life Sciences , Regulatory Affairs , Documentation and Data Management , QA/QC

Residual Solvents: Take Advantage of the New Flexibility in Revised USP <467>
Category: Drugs and Chemicals (Pharma) , Laboratory Compliance , Testing and Validation , Quality and Safety , Laboratory , Analytical Laboratory , Drug Development , Drugs Regulations , Life sciences QA/QC , Research & Development , Drug R & D , Regulations & Guidances , Life Sciences , Regulatory Affairs , QA/QC

Qualification of the Dissolution Apparatus
Category: Drugs and Chemicals (Pharma) , Laboratory Compliance , Quality and Safety , Supply Chain and Manufacturing , Laboratory , Drug Development , Drugs Regulations , Life sciences QA/QC , Research & Development , Drug R & D , Regulations & Guidances , Life Sciences , Regulatory Affairs , Documentation and Data Management , QA/QC

Data Integrity in the Pharmaceutical Laboratory: Practical Steps to Identify and Avoid Data Integrity Issues
Category: Drugs and Chemicals (Pharma) , Laboratory Compliance , Testing and Validation , Quality and Safety , Laboratory , Analytical Laboratory , Drug Development , Drugs Regulations , Audit & Inspection-Role , Lab Audit , Drugs Inspections , Documentation and Policy Management , Lifescience process & Procedures , Life sciences QA/QC , Research & Development , Drug R & D , Regulations & Guidances , Life Sciences , Regulatory Affairs , Documentation and Data Management , QA/QC

New Elemental Impurities Tests for Pharmaceutical Products According to the New ICH Q3D and USP 232/233 Guidelines
Category: Laboratory Compliance

Pharmaceutical Data Integrity Success Training Kit - Pack of 8 Training Courses
Category: Drugs and Chemicals (Pharma)