AUDITING Quality system audits as well as
contractor and supplier audits GMP training – introductory courses and
advanced topics SOP DEVELOPMENT Write Standard Operation Procedures (SOP)
to meet regulatory and client-specific requirements LABEL DEVELOPMENT Devise clinical trial material labels to
meet global regulatory requirements BATCH RELEASES Review of batch manufacturing records and
batch disposition for clinical trial materials CONSULTATION General advice and assistance with GMP
and GLP compliance issues For further information, contact Teresa A. Huddleston at Southwest Quality Assurance Services: info@BiotechQAservices.com, (214) 476-7126.
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Southwest
Quality Assurance Services was set up in 2008 by Teresa A.
Huddleston and specializes in providing GMP and GLP Quality Assurance
services to small and mid-sized pharmaceutical, medical device and biotech
companies. Services include: