Contract Research & Services
Contract Services

Consulting, Auditing and Assessment

By NSF International

NSF International’s unique team of ex-regulatory agency inspectors and highly experienced industry professionals provide authoritative consulting and auditing services to major pharmaceutical and biopharmaceutical companies and regulatory agencies worldwide.

NSF provides in-depth, expert assessment of technical issues and help outsource your entire supplier audit program, as well as specialist services in areas such as cost-effective quality management, manufacturing of major dosage forms including sterile and biotech products, pharmaceutical packaging, clinical trial manufacturing, supply and good clinical practice (GCP), and pharmacovigilance (PV), as well as sterilization procedures, pharmaceutical microbiology, supply chain assurance, good distribution practice (GDP), process and analytical method validation, regulatory compliance for computers and automated control systems, and pharmaceutical water systems.

NSF's pharma biotech can help you with:

  • Preparing for regulatory inspections
  • Due diligence audits for acquisitions
  • QS audits
  • Mock regulatory inspections
  • Good manufacturing practice (GMP) compliance audits
  • Good laboratory practice (GLP), GCP, PV, clinical laboratory improvement amendments (CLIA) and Biotechnology monitoring program (BIMO) audits
  • Over-the-counter (OTC) current good manufacturing practices (cGMP) audits