Why Pharma Companies Must Use Contingent Regulatory Contract Staffing Services

There are several reasons why pharma companies must use contingent regulatory contract staffing services.

Jun 20, 20232 min read

Marketed Pharmaceutical Products Lifecycle Management in Asia

Artixio’s Proven Experience in Managing Lifecycle for Marketed Products in Asia

Jan 21, 20232 min read

Regulatory Information Management Software

Demand for regulatory information management software is growing due to increasing compliance requirements from health authorities.

Jan 10, 20233 min read

Assessing the Regulatory Outsourcing Readiness

Exploring strategies and methods for assessing outsourcing readiness in pharmaceutical organizations.

Jan 6, 20232 min read

Pharma Artwork & Labeling Management Software

From content to carton, a pharmaceutical product's lifecycle includes scientific medical writing from product development (target product pr

Jan 4, 20233 min read

External Drivers for Regulatory Outsourcing

A Summary of scenarios that enable regulatory outsourcing requirements pharmaceutical and medical devices industry globally.

Jan 4, 20234 min read

Regulatory Outsourcing Scenarios

Regulatory departments within biopharma companies decide work with an external partner for one or more reasons, Need for specialized...

Jan 4, 20232 min read

Document Management Systems (DMS) for Pharmaceutical Industry

A 21 CFR Part 11 compliance DMS is part of overall compliance and quality requirements across pharmaceutical organizations.

Jan 4, 20233 min read

Insights

Global, Concurrent, Experience Based

Deep dive and engage in insightful discourse driven by concurrent global regulatory scenarios, industry trends and Artixio’s real-time experience across the product value chain. Whitepapers, research articles, landscape reports and case studies to help you stay ahead of the curve.

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