We help our clients achieve Total Quality Assurance through customized, flexible, contract services. Our scientists, auditors and regulatory experts work with you at every stage of development, providing GMP and CMC Laboratory Services, Biopharmaceutical Development Support, Medical Device Development Support, GMP Auditing, GLP/GCP Bioanalysis, Regulatory and Toxicology Consulting, and Pharmaceutical Manufacturing Support. We have delivered flexible Total Quality Assurance contract services to the global pharmaceutical industry for over 30 years and currently provide high-quality technical services to some of the world’s largest and most innovative pharmaceutical companies.

GMP and CMC Laboratory Services: Regulatory-driven, phase-appropriate laboratory services in support of CMC programs. Our regulatory labs include centres of excellence for method development and validation, analysis and characterisation for biologics, mRNA, oligos, cell and gene therapies or vaccine products, inhaled product development, nasal drug development, ICH stability testing and storage, extractables and leachables, formulation development, clinical trial materials manufacturing, cGMP quality control testing, and cGMP batch release testing.
Bioanalysis Services: In addition to conducting regulated bioanalytical studies for small and biologics, we provide biomarkers services.

Learn more: www.intertek.com/pharmaceutical
https://www.intertek.com/pharmaceutical/analysis/inhalation-product-development/
https://www.intertek.com/pharmaceutical/analysis/stability/
https://www.intertek.com/pharmaceutical/analysis/extractables-leachables/
https://www.intertek.com/pharmaceutical/biopharmaceuticals/