Our state-of-the-art laboratories offer a wide range of analytical services to support your exact needs under strict quality procedures which meet GMP requirements and following ICH guidelines.
The analytical department provides support during the development of drug formulations combining modern instrumentation and the advanced knowledge in the field of analytical science as well as validation services across a range of analytical activities.
The instrumentation used follow the GMP requirements, such as the annual operational and performance qualifications as well as the requirements for computerised systems and data integrity.
Lamda’s analytical options are available on a stand-alone bases or as part of a full development package.
We devise and implement product specific development strategies capable of delivering high-quality formulations and robust manufacturing processes.
In applications for Generic and Generic Plus medicinal products, the concept of bioequivalence is fundamental.
Continuous evolution in science and changes in the regulatory environment and health sector, creates the need for professional regulatory guidance throughout the lifecycle of a healthcare product.