Organic Volatile Impurity Analysis (OVI)
The identification and quantification of residual solvents (RS) and organic volatile impurities (OVI) in pharmaceutical products.
There are many different solvents used in pharmaceutical manufacturing. Intertek pharmaceutical laboratories assure clients that organic volatile impurities and residual solvents have been reduced to the acceptable level in manufacture of drug substance, excipients and drug products. Methods utilised include pharmacopeial methods (e.g. USP <467>) but methods can also be developed tailored to our client's specific needs. These services can be applied to product development support and also in GMP QC release testing.
Organic Volatile Impurity Analytical capabilities include:
- Headspace GC or GCMS
- Gravimetric techniques
- Method development to ICH guidelines
Related Pharmaceutical Analysis Services:
Request more information to see how Intertek can help your organization with Organic Volatile Impurity Analysis (OVI).