Chairman's Message"At Protech we believe that meaningful innovation should support, nurture and protect life from ailments, diseases, deformities. The knowledge of technology should harmless the potential of innovation and reach its benefits to the common man. Only then research in Pharma can become meaningful for the society as a whole"
Production Facility -
" BEST QUALITY AT ECONOMICAL PRICE " is the motto of Protech Production.
Protech manufacturing plant is well equipped with most sophisticated, ultramodern and latest state of art machinery and maintaining strict INTERNATIONAL STANDARDS at all steps of manufacturing & packing.Our manufacturing facilities confirm to the stringent standards of cGMP W.H.O. standards. Products are manufactured under strict humidity control, temperature control & good hygienic conditions. The drugs are manufactured under the supervision of technically highly qualified and competent people having Masters Degree in pharmacy, Bachelor Degree in pharmacy. These technocrats can only maintain the minutest aspect of quality so that the stringent standards mentioned in Pharmacopoeia can be met with and patient will get complete relief from his ailment. Empty gelatin capsules tested for microbial contamination before filling. Leak test is performed on blister strip.
Each & every step of production process is under continuous monitoring & control, independently by the sections changing out an activity & counter checking by QC & QA.
All raw material & packing are tested in Q.C. lab as per specification only after their approval taken to production purpose.
The whole water system including water treatment is periodically tested for physicochemical & microbiological parameters as per laid specification & the water meeting the quality standards is only used for production progress.
The raw materials for a batch of a product and its bulk preparation is counter checked by QC, QA & only after analyzing of the bulk solution & it meeting the laid specification, the same its processed further. The polyethylene granules used for formation of containers are tested in QC lab for physicochemical & pharmacological characteristics as per laid specification.
The containers being formed /filled & sealed are being tested for uniformity of contents as well as weight of individual containers & other quality characteristics regularly and at periodic intervals.
The form filled /sealed containers are subjected to leak testing on semiautomatic machines. All good leak tested containers are further subjected to visual inspection individually. All visually good containers only are allowed for final packaging.
Representative samples of filled/ sealed container are taken for the finished product analysis (physicochemical, sterility, bacterial, End toxin, toxicity).
During all the stages of production stages pre and post line clearances are carried out to avoid any cross mix-ups.
During packaging operation, random checks are carried out to ensure correctness of all stages & materials used.
- Representative samples at packing stage are taken out as retain samples & retained.
- The products are inspected under written instruction prior to dispatch to market.
- All the process control steps are recoated in the respective documentation system