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40% Faster Validation Cycle

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Complete Instant Traceability

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Industry Insights

Articles for improving efficiency and processes.

VALIDATOR WHITE PAPER - Quality by Design (QBD) for Process Validation

The Pharmaceutical industry is a heavily regulated industry. It is most evident during the New Drug and Abbrievated Drug Application Process. The large amount of documentation required during this submission phase consumes a considerable amount of time and resources to prepare.

VALIDATOR WHITE PAPER – Addressing 21 CFR Part 11

21 cfr Part 11 has been become a very large concern in the pharmaceutical industry as of late due to pressure  from regulatory bodies enforcing compliance for GxP systems. Due to this, more and more organizations are realizing the criticality of employing or ramping up existing system to meet these requirements.

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 ABOUT US 

Compliance Associates

Compliance Associates is your partner for regulatory compliance. With over 25 years of experience, we are the most knowledgeable and dedicated company in the industry. We provide solutions that optimize compliance and regulatory infrastructure. By leveraging existing operating technologies and business processes, we cost effectively meet compliance requirements leaving our clients free to focus on their core business-and building on their bottom line.

Validator, our industry leading compliance solution, is a true content management system that allows companies to automate the entire lifecycle of validation, for any type of validation project. It’s built specifically for validation and is the only truly automated compliance solution available.

Find out how Compliance Associates and Validator can help your organization today. Email us at info@complianceassociates.ca or call 905-738-3773 to request a product demo or to set up a meeting.

 

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   Validator is invaluable to us. With it, we have a far more efficient process overall.

Eric David, Director Development Translational Medicine at Biogen

 
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