An API portfolio elevated by Verilege™

Ensure quality from start to finish. We deliver consistent, high-quality APIs across our global network through:

• cGMP-certified facilities adhering to the highest manufacturing standards.
• Robust quality control processes.
• ICHQ7 compliance for reliable pharmaceutical-grade active ingredients.
• Continuous investments, with regular inspections by various authorities. 

Simplify the drug filing process and path to approval with comprehensive regulatory dossiers, best-practice sharing, and customized support.

• Up-to-date dossiers for global registrations—such as CEPs, US DMFs, Japanese DMFs, and China DMFs—along with access to the API section of marketing authorization approvals worldwide.
• Standard and customizable statements.
• Personalized assistance with regulatory submissions and documentation to ensure compliance with ICH, US FDA, EMA, and other regional standards.
• Regulatory documentation gap assessments and regulatory strategy expertise.

Together, we’re not just advancing patient health—we’re driving sustainable progress. We can help you achieve your sustainability goals, including Scope 3 targets.

• ISO 14040/44-compliant Life Cycle Assessments (LCAs).
• Transparent data sharing, including primary data, sustainability targets, and certifications (EcoVadis, SBTi).
• Proprietary tools, like the Imp’Act Card™ program, provide science-based metrics on the environmental footprint, traceability, and social impact at an ingredient level.
• Expert support for sustainability questionnaires, emission calculations, and co-developing sustainable solutions.

We ensure access to high-quality APIs via a worldwide network of strategically located production facilities. Assuring delivery against GDP requirements, we help de-risk your supply chain, and support your drug development pipeline.