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Validation Documentation Completed for Regulatory Compliance

Upgrades to hardware and software systems at WDSrx increase efficiency and capabilities for clients.

Each point of access connecting to WDSrx internal systems must be validated for Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ) to assure pharmaceutical 3PL compliance with 21CFR210/211 guidelines.

Validation projects are managed by the WDSrx Regulatory Compliance team.

Proper validation documents are made available when requested for client audits and regulatory authorities.

Click here to learn more.

The WDSrx Regulatory Compliance team oversees validation projects.

Are any Controlled Substances (CII) included in your return? If so, please press "Yes" and complete the DEA 222 Request Form. You can also contact Jason Solomon at jsolomon@wdsrx.com or (561) 998-3885 x316.