The RAPS store will be under maintenance Saturday, 28 September between 6 a.m. and 12 p.m. Store functionality may be unavailable at times during this window.
We apologize for any inconvenience caused during this time.
||Bennett and Company provides a variety of regulatory and quality system consulting services to companies worldwide. With more than thirty years of experience within and outside of FDA, Martha Bennett assists companies with compliance, product approval, and post-marketing issues. Using risk-based management tools (e.g., Six Sigma, FMEA, HACCP), Martha assists companies with validation strategy, planning and education. A skilled communicator and effective trainer, Martha also conducts FDA and quality focused training. Thoroughly grounded and experienced in FDA law and regulations, Martha also provides consulting services to legal team as well as expert testimony.
107 S. West Street PMB 730
Alexandria, Virginia 22314
Martha M. Bennett
Cellular & Gene Therapy
Cell & Tissue Products
|Professional Responsibility (Production):
||Conception and Development
|Professional Responsibility (Regulatory Process):
||Good Laboratory Practice (GLP)
Quality System (QS)
Good Clinical Practice (GCP)
Good Manufacturing Practice (GMP)
Biological License Approval (BLA)
Investigational New Drug (IND)
Investigational Device Exemption (IDE)
New Drug Approval (NDA)
Premarket Approval (PMA)
Premarket Notification (510k)
|Other Professional Responsibility:
||Crisis Management/Risk Management