CDMO
Advance your molecule from discovery to manufacturing with our expertise
We have extensive chemistry capabilities in synthesis/manufacture to advance your API from concept to manufacturing. We can provide you the required quantities of non-GMP/GMP grade Key Starting Materials (KSMs), Advanced Intermediates and Active Pharmaceutical Ingredients (APIs) from our established infrastructure. This enables your reliable supplies to drive your program across the preclinical and clinical development and commercial launch.
With an experienced team, we have earned the trust of our customers. This has been achieved with an established track record of successful and timely delivery of their projects. Our team has the ability to identify potential challenges encountered in process development and find innovative solutions in the process development stage. Our team of process engineers backed by an excellent engineering and design team ensures efficient transfer of process from the drawing board to reality. Every project is seen as a new project to learn. The team also brings the experience from the delivered projects to ensure successful delivery. All this, ensures our customers’ need for timely availability of drug substance to accelerate their development projects from pre-clinical to global clinical trials and commercial launch.
Our integrated manufacturing facility is equipped with other support services like Project Management, Engineering, EHS, Quality Control, Quality Assurance & Regulatory, Supply Chain Management to ensure reliability of operations and efficiency.
Process Development / Optimization
INVENTYS’s multi-disciplinary process development team can quickly absorb the tech-package that is shared by our clients. The team is extremely adept in evaluating the information and find creative ways of improving the process on need basis. The team evaluates the details related to route-scouting, scale of operations performed in the tech package. We have demonstrated the ability to suggest subtle changes which has translated into immense benefits in terms of batch cycle time, costs without compromising on the quality of the compound. Our ability to backward integrate also ensures reliability of supply and reduced cost of goods. We can also adopt the principles Quality by Design for late phase chemical development as required to drive the last stage clinical development projects. Our technical team is also backed by an able analytical team to provide all the necessary support in this stage.
We are well positioned to support our customers in accelerating their drug programs. We can provide the required quantities of Key starting materials (KSMs), advanced intermediates and NCE APIs with our expertise, infrastructure and our experienced team.
Contract Manufacturing
INVENTYS manufacturing facility is WHO GMP certified. We are also ISO-9001, ISO 14001 certified. Our systems are designed and operated to meet our customers’ regulatory expectations. Our systematic approach ensures that we absorb the tech-package from our clients and also improve the overall process efficiencies. We can thus drive the contract manufacturing from development phase with this experienced and dedicated team.