We envision to provide quality and transparency in our services for partners and to enable them conduct next phase of drug development activities. We strive for excellence in our chemistry through knowledge and hard work. We consistently improve our processes to bring better technologies that will help patient outcomes. We further pay utmost regard to our customers goals and act with speed and responsibility.
We will dedicate chemists to perform customer projects and conclude the results based on predefined terms.
We also help steer projects from external CMO and perform a technical transfer of the process.
We will synthesize reference standards based on the phase of your drug development. This can be purification or synthesis or both.
We offer custom synthesis of your final API and execute the chemistry based on intended specifications for each intermediate.
We also offer drug discovery services using our expertise in medicinal and synthetic chemistries.
We have extensive accomplishments, background and experience of process chemistry and scale up, for different phases of drug development.
We manage chemistry and manufacturing activities with external CMO’ for small and virtual biotech’s for their drug substance supply needs.
Designing validation, based on CPPs, risk mitigations, PFMEA analysis and historical GMP results is imperative.
We will dedicate chemists to perform customer projects and conclude the results based on predefined terms.
We also help steer projects from external CMO and perform a technical transfer of the process.
We will synthesize reference standards based on the phase of your drug development. This can be purification or synthesis or both.
We offer custom synthesis of your final API and execute the chemistry based on intended specifications for each intermediate.
We also offer drug discovery services using our expertise in medicinal and synthetic chemistries.
We have extensive accomplishments, background and experience of process chemistry and scale up, for different phases of drug development.
We manage chemistry and manufacturing activities with external CMO’ for small and virtual biotech’s for their drug substance supply needs.
Designing validation, based on CPPs, risk mitigations, PFMEA analysis and historical GMP results is imperative.
We will dedicate chemists to perform customer projects and conclude the results based on predefined terms.
We also help steer projects from external CMO and perform a technical transfer of the process.
We will synthesize reference standards based on the phase of your drug development. This can be purification or synthesis or both.