At Agile Scientific, we understand that clinical development is continually evolving, and it’s becoming increasingly more important for companies to keep up to date with changes to regulatory requirements. To this end, it’s vital to have systems in place that both function efficiently, and comply with all existing domestic and international regulatory requirements, and if your company needs help to remain competitive and compliant, we can certainly help you achieve that.
Clinical quality processes are vital for helping companies to build a good reputation within their own organization, and with regulatory authorities, and with our assistance, we can help you expertly create an effective clinical quality process or system, or guide you through objectively assessing your existing systems.
Below are just some of the procedures and practices that our Quality Assurance service can help you with:
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- Every aspect of GCP, GMP and GLP auditing
- Pharmacovigilance Audits
- Mock Audits and Inspection Readiness
- Clinical Study Report Review and Auditing
- Computer Systems Validation
- Strategic Process Development
- SOP and Protocol Design, Development and Review
- CAPA Development
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Contact
Phone
+1.317-644-1613
info@agilescientific.net
Address
6555 Busch Blvd, Suite 245,
Columbus, OH 43229