GLP, GCP, CLIA and BIMO Audits
- Why Work With NSF?
NSF Pharma Biotech’s team of expert consultants is experienced in conducting Good Laboratory Practice (GLP) and Good Clinical Practice (GCP) audits, Clinical Laboratory Improvement Amendments (CLIA) assessments and Bioresearch Monitoring (BIMO) audits in order to assure compliance with regulatory requirements and industry best practices for laboratories and clinical research. Our consultants can conduct gap analyses, mock regulatory agency inspections, training and other activities to ensure that research and laboratory standards are met.
Why Work With NSF?
Our team of former regulatory agency staff and current R&D professionals and laboratory scientists has the breadth of knowledge, experience and skills to ensure that you receive a best-in-class audit of your laboratory and clinical activities, wherever you are in the world.
NSF Health Sciences cordially invites you to join us at SOT When: March 13-17, 2016 Where: New Orleans, LA USA...
- 1 month ago
FDA Regulatory and Compliance News FDA announced the availability of a draft guidance for industry and FDA staff entitled, “Public...
- 2 months ago
FDA Regulatory and Compliance News FDA announced the approval of Torax Medical’s Fenix Continence Restoration System to treat fecal incontinence...
- Friday, February 26, 2016
- 11:00am - 12:30pm Eastern Time
- Wednesday, March 2, 2016
- 8:30am - 5:00pm GMT
- Manchester, United Kingdom
- Tuesday, March 8, 2016
- 8:30am - 4:00pm GMT
- Manchester, UK, United Kingdom
- Monday, March 14, 2016
- 8:30am - 3:00pm GMT
- York, United Kingdom