Stay informed with the latest insights on pharmaceutical regulations, industry trends, and best practices in RLD sourcing, technology transfer, and strategic partnerships.

Secure comparator sourcing for clinical development
RLD Sourcing Clinical Trials

Comparator Integrity: The Backbone of Reliable Clinical Trials

Why Reference Listed Drugs must be sourced with traceability, the documents regulators expect to see, and how Tanimswiss Pharma safeguards every shipment from purchase order to patient dosing.

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Regulatory GDP compliance tips
Regulatory GDP

Five GDP Habits That Impress EU Inspectors

From temperature mapping to partner qualification, learn the daily disciplines that keep distribution networks audit-ready and protect product quality across continents.

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Technology transfer collaboration
Technology Transfer Operations

De-risking Technology Transfers with Digital Readiness Assessments

How data integrity reviews, equipment comparability matrices, and blended on-site / remote training accelerate transfers without compromising compliance.

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Global dossier strategy
Dossier Strategy Generics

Designing Dossiers for Dual EU & Emerging Market Submissions

Practical guidance for harmonizing CTD modules, leveraging bridging studies, and planning artwork workflows when one development program feeds multiple agencies.

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Strategic pharma partnerships
Partnerships Business Development

Licensing Models That Unlock Faster Market Entry

Comparing out-licensing, co-development, and revenue-share models, plus the KPIs Tanimswiss Pharma uses to evaluate mutually beneficial collaborations.

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Supply chain resilience
Supply Chain Risk Management

Building Resilient Pharma Supply Chains for 2025 and Beyond

Lessons learned from global shortages, how dual sourcing and digital temperature monitoring mitigate risk, and the metrics investors expect to see.

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