Quality and Regulatory Compliance

Our policy for quality
Southern Research Institute provides products, processes and services of the highest possible quality on a timely basis, that meet or exceed the requirements and expectations of its clients and customers and that are in compliance with applicable laws and regulations.

• Institute-wide focus and dedication to quality performance, continuous process and systems improvement, and pursuit of customer satisfaction.
• Drug Development/Safety Assessment and Pharmaceutical Formulations groups are compliant with Good Laboratory Practices (21CFR part 58) and Good Manufacturing Practices (21CFR parts 210-211).
• Documented procedures for planning, implementing and performing internal ISO, GLP and GMP audit inspections for continuous compliance monitoring.
• Certified International Registry of Certified Auditors and Registered Quality Assurance Professional Auditors constitute the Quality Assurance Department and deliver ongoing training programs and regulatory and quality system audits.

Related Links
Food & Drug Administration
American Society for Quality
Quality Digest

Quality Assurance - Engineering:
Courtney Kerr
205-581-2303
kerr@southernresearch.org

Quality Assurance - Good Laboratory Practices:
Carol Hoffman
301-694-3232
hoffman@southernresearch.org