The Veeva audit team (AIM) provides a variety of informative documents from regulatory assessment to system and process overviews. Somewhere between the assessment and the overview is a space for an article: The article operates in this between and shares with the editorial the form of a learned opinion. An article is (on the one hand) one of the smallest units of grammar, whether definite or indefinite, the article qualifies the noun (and the subject at hand). On the other extreme (of verbosity), a journal article can elaborate extensively on a given theme. And then again, an article of incorporation (or association) is generally regulative, that is to say it regulates the subject at hand (i.e., a company, a government, or association).

Process Area Relevant Articles
Contracts and Agreements - Quality Addendum for Multi-tenant SaaS Software Deployments
Quality Operations - Boundary Conditions of the QMS
- Business Continuity Management
- Process Maturity: A CMMI Perspective
- The Problem of Recoverability in Multitenancy
- The Veeva QMS on an ISO Document Hierarchy
- Titles, Roles, JDs and other RACI Concepts
- Top x Reasons Veeva Does Not Distribute its P&P to Customers
Computer System Validation - Change Notification
- Computer System Compliance Deconstructed
- Customer Periodic Review Requirements
- Data Migration
- Defects, Deficiencies, and Deviations
- Limitations of Product Validation
- Mastering Product Validation Review
- Our Requirement for Meaning
- Philosophy on Validation of Business Systems
- Rebaseline Revisited
- SaaS Maintenance Releases & Patches
- Validation Defined
- Vault Validation Tips and Tricks
- What is a Good Test Script (GTS)
- What is a(n ERES) System
Audits and Inspections - Access to Veeva Internal Records: Limitations
- Audit Finding Acceptability Criteria: The World According to GARP
- Audit Support: Drawing the Party Lines
- Audit vs. Inspection To be or not to be
- Auditing IT Services Vendors
- Customer Audit Support
- Hosting a Regulatory Inspection of SaaS
- SaaS Shared Responsibility
Regulatory Compliance - 6 Degrees of Separation from Predication
- Backups, Archives, and Retention
- Below de-Bar
- Certificate of Part 11 Analysis
- Choosing the Right SOC
- Clinical Protocol Training Requirements Unpacked
- Data Center Locations
- EMA Q&A Review
- eSigning on the Event Horizon
- GxP Backup Requirements
- IF all CRO are Vendors, THEN…
- Incident Management Process
- Taking GCP Breach Notification Seriously
- The Order of Things On Classification
- Trial-Related Duties: Entering the Transfer Portal
- What is a Reasonable Audit Trail
- When is an audit trail not an Audit Trail