The facility is designed to comply regulatory norms as per Schedule M, WHO GMP and PIC’s standards. A fine tuning further can get Smith and Kenner Pharmaceuticals credentials upto MCA, TGA and EU GMP. The Unit has a live WHO GMP license and more than 30 products having COPP The total construction area of the Unit is closed to 45000 sq mtr. The entire facility consists of 3 major parts 1. βetalactum Oral Solid dosages 2. Non βetalactum Oral solid dosages . Liquid and Elixir dosages and Tropical preparation 3. Utilities. The unit is designed as per the Schedule M regulations which is being practiced inside the facility at all the work stations. The entire facility is made out of Epoxy flooring and man and material entry is restricted through dynamic pass boxes where the chance of cross-contamination is seen.
The capacity of Oral Solid dosages is approximately 2 million tablets of 585 mg per day in a shift of 8 hours. Dry sachet formulation area where electrolytes and Oral rehydration products are being manufactured. An area with a blender and 5 form fill and seal machines take the job of filling 5 gms to 100 gms of any blend product.The daily capacity of such products of 30 gms can be around .10 million sachets. Liquid area is having a capability to manufacture 3 KL of any product. Approximately 1.5 million bottles of 100 ml of finished product can be taken from this area in a month consisting of 25 working days. The other section of Betalactum block is again constructed as per the box – in – box technology. The area is specially designed to manufacture highly hygroscopic materials such at Clavunate potassium, ceftatidine, Cefipime and any other materials needs temperature below 20 and RH below 40. The facility has complete area under forced lights as per LUX and HVAC as per the need of the area. The βetalactum block is capable of manufacturing Oral solid dosages and dry syrups.The unit has unique manufacturing technique under the hands of qualified professionals. Modern quality control department is equipped with HPLC, UV and all required instruments to meet the day to day requirement of the products.
Qualified personnel take special care of the documentation and a team of QA personnel look after each aspect of the product and assures a quality product from Smith and Kenner Pharmaceuticals. The utility sections consists of a DG set to give power back up to the entire Unit, DM and RO.
We at Smith and Kenner Pharmaceuticals practice GMP and bring GMP into practice.Smith & Kenner also has license to manufacture Narcotic drugs such as Pseudoeffedrine + Triplopidine Codeine + CPM Effedrine May we look forward for your kind consideration in manufacturing your valuable products under LL or 3 rd Party based on your needs.
| Business Type | Manufacturer, Exporter |
| Year of ESTD | 1983 |
| Company Turnover | Rs. 2 - 5 Crore ( or US$ 400 K - 1 Mn Approx.) |
| Ownership Type | Pvt Ltd Company |
| No of Employees | 11-20 People |
| Major Markets Cover | African Countries, Gulf, Europe, Asia |
| GST No. | 36AACCS8118A1ZO |
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