To become a cost effective and quality manufacturer.
Conform to the highest standards of ethics and business integrity. Transparency with our customers, vendors and employees. To provide pollution free zone to employees and public. To satisfy the customers w.r.t quality, services and cost competitiveness.
Developing novel process for intermediates.
Process development.
Minimization of effluent and improving the safety.
Scale-up of any complex molecule as par with lab yields and quality.
Trouble shooting & Safe operational development for all hazardous activities.
We follow CGMP and ready for all third party audits.
We will provide the documents for CMC (Chemical manufacturing control) section, if required, for submission of DMF.
For all high value, key intermediate supplies, we will conduct the use test in addition to regular analysis to avoid any undesired results in the Pharma stage.
We will provide stability data for all key raw materials of regulatory products for submission of USFDA/ other regulatory authorities.
We shall keep the relevant Impurity samples available to support the customers.
Prospective process and drying validations.
Preventive maintenance for all process equipments.
Good house keeping.
On-line documentation and temperature data logging for all equipment.
Change control, deviations and quality trend are being monitored for traceability.