Ataqua Regulatory Services
Verifying Regulatory Compliance
ARS can help you establish GMP quality management systems, develop new products, develop and validate analytical test procedures, provide support after receipt of a FDA Form 483 or warning letter, and more.
ARS can conduct audits to verify your organization’s compliance to GMP requirements or to determine the effectiveness and efficiency of your operation to promote continuous improvement.
ARS can provide remote or in-house training at your facility, customized to your specific business needs.
Ataqua regulatory services’ mission is to provide superior regulatory and scientific advice and services to help clients manufacture quality healthcare products for consumers and comply with applicable regulatory requirements. ARS is a woman-owned disabled veteran company.
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