info@spectrogen.co.in
+91 40 35035220
info@spectrogen.co.in
+91 40 35035220
Our company manufactures formulation products through Third Party Manufacturers are multiple dosage forms, including oral solids, oral liquids, dry syrups and injectables. We sale the formulation products in the Generic Market and Ethical Market. Our Company sells domestic products through our Pan-India network of distributors, stockiest and pharmacies, The network process is, we supplies the Finished Goods from Third-Party Manufacturers to the C&F Agents. From the C&F Agents, the Stocks are supplied to the Stockists, Sub-Stockists, and Hospitals. The Retail Pharmacy obtains products from the Stockists / Sub-Stockists through whom it finally reaches the Consumers.
Our Analytical services is engaged in providing the following services to the customers are as under
The Company conducts the Dissolution Studies for the purpose of Bioavailability and Therapeutic Effectiveness. Dissolution is the process in which a substance forms a Solution. Dissolution Testingmeasures the extent and rate of Solution Formation from a Dosage Form, such as Tablet, Capsule, Ointment, etc.
Stability Testing is an integral step to developing New Pharmaceutical Products and Active Pharmaceutical Ingredients, to establish their Shelf-Life or Expiry Date. It is also equally important along with ongoing routine manufacturing to monitor Product Quality as a function of time. We provide a complete solution to your requirements ofStability Studies for Shelf-Life Estimation.
Microbiological Testing plays an important role in the production of Pharmaceutical Drug Substances and Drug Products. Pharmaceutical Microbiological Testing is essential for Patient safety as the Patients consuming the medicines might already be in a compromised position and easily susceptible to infections. Our MicrobiologyTesting ensures that the Raw Materials used in Drugs match the Standard Quality Requirements before they are processed in the production environment.
Our Microbiologists also validate the methods used for testing Finished Products as well as monitor the quality of air and water from the Microbiological Perspective. We provide Pharmaceutical MicrobiologyTesting Servicesto manufacturers of both Sterile and Non-Sterile Pharmaceutical Products and Substances. Our Laboratories are well equipped and carry out all the required Microbiological Testing for Pharmaceutical Industry.
Sterility Testingis an essential microbiology testing requirement that ensures that the Sterile Pharmaceuticals, Medical Equipment and Substances are safe for use.
Limulus Amoebocyte Lysate (LAL) Test is performed to check and quantify Bacterial Endotoxins that are extracted from the products.
Microbial Contamination Testing is performed for Non-Sterile Products in which Harmonised Pharmacopoeia or Client-Supplied Methods are used that determine the Bio-burden within the sample.
Total Bacterial Count indicates the number of Microorganisms present in a sample. The number of Microorganisms should not be greater than the specified guide values that are expressed in CFU (Colony-Forming Units) Per Gram or Milliliter.
It indicates Fungal Count present in a sample. Monitoring this is important to know about the Fungal Contamination in Pharmaceuticals.
Detection of Pathogens in Pharmaceuticals Finished Products and Raw Materials is important for the safety and well-being of the Consumers.
This is done to determine the efficiency of Antibiotics.
This Test is done to determine the Potency of Vitamins.
It is used for the Total Viable Count. It is important to ensure that the product is fit for human consumption.
This Test is performed to check the type and minimum effective concentration of preservative that is required for satisfactory preservation of Pharmaceuticals.