We're here to help people live their best lives!
We believe in our brand. We're proud of our history. And we take responsibility for everything we've done.
- We're an international provider of testing, inspection, and certification services.
Knowledge & Education: Get more training webinars, white papers, blog posts, regulatory resources, product directories, client portals, and standards from Intertek SAI Global.
- Depending on which side of the fence you're on, some companies may view certification as an obstacle they need to overcome before releasing their product into the marketplace. Other companies may see certification as a necessary step for reducing risk or liability.
We're available worldwide!
- We're the industry leader, with offices in over 100 different locations worldwide. Whether your company is local or global, our experts can help to ensure that its products meet quality, health safety, environmental, and social standards for virtually any country around the globe.
Testing, laboratory, stability testing, development, team, analysis, documentation, validation, quality assurance.
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Analytical Research and Development, formulation development, analytical development environment, analytical method development, - Compliance Policy Guide, level of compliance, regulatory compliance programs, activity for compliance.
Core Team, inspection team, monitoring team, project team, larger sample, sample mix-ups, sample size, reference standards, must-have reference, reference list, extensive industry experience, Industry Edge, medical device industries, Legal requirements, time commitment, agreeable time, analytical instruments.
Analytical instrument life-cycle, drug substance, molecular weight drug substances, active drug substance, sequence of analysis, reporting practices, electronic data documentation, accurate documentation, methods validation, coverage of drug regulations, pharmaceutical regulations, technical expertise, additional expertise, real-world case studies, stability studies, table of contents, acceptable content uniformity results.
We offer GMP Analytical laboratory.
Intertek offers pharmaceutical analyses that comply with Good Manufacturing Practices (cGMP) regulations for pharmaceutical products throughout their life cycle. These include analytical methods for characterizing drug substances, excipients, finished dosage forms and biological fluids.
We provide scientific expertise to help develop your products for both small molecules and biologics, including protein therapeutics, monoclonals and vaccine candidates. We have extensive experience designing and developing drug formulations and medical device technologies.
cGMP Compliant Analytical Laboratories:
Intertek Pharmaceutical Services specializes in cGMP analytical R&D, inorganic and organic element analysis, product stabilization and extractable/leachable analysis. The lab is GLP and cGMP compliant, and was added to the World Health Organization's prequalified quality control labs program in 2014. Intertek Pharmaceutical Services Manchester specializes in cGMP analysis, process analytical technologies, and advanced characterization. Its services include cGMP NMR spectroscopy, GMP batch release tests and drug product formulation. Intertek Melbourn specializes in analytical and formulation chemistry, including analytical methods, process analytical technologies, product characterization, formulation design, and GMP manufacturing. Its staff includes chemists, biologists, engineers, statisticians, and quality assurance professionals.