Enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes.
Evaluating how your products and services meet and exceed quality, safety, sustainability and performance standards.
Validating the specifications, value and safety of your raw materials, products and assets.
Connecting with the Korean and East Asia pharmaceutical sector, Intertek experts will exhibit at KOREA PHARM 2016
During Korea Pharm 2016, our experts in laboratory CMC support programs such as method validation, pharmaceutical analysis, stability, extractables / leachables and bioanalytical support for preclinical and clinical development, will be available at exhibition booth 9D308 to discuss current projects or future requirements.
In particular, during Korea Pharm, we shall highlight, our specialist expertise for biopharmaceuticals such as proteins, monoclonal antibodies, biosimilars, ADCs and more. Contact our team now to arrange for an updates on our latest expansion and investments in technologies such as Luminex or SPR.
With a focus on providing expert regulatory-driven, analytical and bioanalytical services to support both small molecule and biologic medicines, our laboratories are dedicated to helping clients the challenges of drug development and manufacturing. Over the last 20 years, the Intertek network of Good Laboratory Practice (GLP) and Good Manufacturing Practice (cGMP) laboratories has provided high-quality technical services for some of the world’s largest and most innovative pharmaceutical companies.
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