Quality Policy
Quality Manual
With congenial working environment; strong infrastructure; highly skilled and dedicated technical staff & committed management work to maintain updated Quality Management Systems; that have resulted in compliance with the highest standards, of quality safety and productivity.
We are specialized in small and medium sized all forms of formulations such as Tablets, Capsules and Liquid Orals. We have the additional capability of packaging the product in bottles, jars, and pouches, or bulk packaging in drums and pails etc.
We have full-fledged Quality Control Laboratories with separate areas for Chemical, Instrument, Microbiology, Sterility and Package testing. Our laboratories are well equipped with sophisticated instruments like Dissolution testers, UV-Visible spectrophotometers and LAF units. These instruments are calibrated periodically to check their performance so as to avoid any manual errors.
Our Quality Control and Assurance team consists of highly experienced and qualified personnel having expertise in various disciplines like Chemistry, Microbiology, Pharmacy and other relevant areas
The process of Quality Control and Quality Assurance starts right from the stage of procurement of raw material to delivery of finished product. Each raw material, packaging material and finished product goes through stringent quality checks. As part of the Quality Control and Assurance process, a Standard Operating Procedure is in place which forms the guideline for the procedures to be followed for each activity that is performed in the plants and laboratories. The development process for any formulation ensures strict compliance with cGMP.
Every raw/packaging material received at the manufacturing sites is procured only from well established and approved manufacturers or suppliers. Approved vendors are judged by a vendor audit or by evaluating their yearly performance.
Each raw/packaging material is sampled and analyzed by Q.C. before releasing for production.
We at SOTAC pharmaceuticals strongly believe that the very-ground, for any pharmaceutical company to survive & prosper, is the in depth & direct perception of quality in every process of Pharmaceutical formulation.
We have our own in-house, sufficiently equipped & fully functional Instrumental analysis Laboratory, Wet analysis laboratory & a separate Microbiological testing laboratory. However wherever needed we also utilize the services of other reputed laboratories for carrying out the various tests.
The modern well equipped Quality Control laboratory was established to ensure that the products are pure, safe and effective and is released only after thorough analysis as per stringent specifications, methods and procedures developed in line with international guidelines.
We only use high-grade, quality consistent raw materials procured from the leading bulk drug manufacturers used in all of our operations. We supply all formulations in the various permitted/suitable dosages and the required pack sizes in various forms such as tablets (uncoated, sugar coated, enteric coated, film coated, chewable, sustained release and dispersible forms), capsules, liquid orals and topical lotions for external applications.
Our manufacturing operations are carried out under the most controlled of environments where quality is a prized ideal. With cutting edge machinery & excellent quality control, we work to ensure that manufacturing is carried out in a safe and reliable manner.
With congenial working environment; strong infrastructure; highly skilled and dedicated technical staff & committed management work to maintain updated Quality Management Systems; that have resulted in compliance with the highest standards, of quality safety and productivity.
We are specialized in small and medium sized all forms of formulations such as Tablets, Capsules and Liquid Orals. We have the additional capability of packaging the product in bottles, jars, and pouches, or bulk packaging in drums and pails etc.
We have full-fledged Quality Control Laboratories with separate areas for Chemical, Instrument, Microbiology, Sterility and Package testing. Our laboratories are well equipped with sophisticated instruments like Dissolution testers, UV-Visible spectrophotometers and LAF units. These instruments are calibrated periodically to check their performance so as to avoid any manual errors.
Our Quality Control and Assurance team consists of highly experienced and qualified personnel having expertise in various disciplines like Chemistry, Microbiology, Pharmacy and other relevant areas
The process of Quality Control and Quality Assurance starts right from the stage of procurement of raw material to delivery of finished product. Each raw material, packaging material and finished product goes through stringent quality checks. As part of the Quality Control and Assurance process, a Standard Operating Procedure is in place which forms the guideline for the procedures to be followed for each activity that is performed in the plants and laboratories. The development process for any formulation ensures strict compliance with cGMP.
Every raw/packaging material received at the manufacturing sites is procured only from well established and approved manufacturers or suppliers. Approved vendors are judged by a vendor audit or by evaluating their yearly performance.
Each raw/packaging material is sampled and analyzed by Q.C. before releasing for production.