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Packing Size Available
Himgange Ayurvedic Oil 2.5 ML
Himgange Ayurvedic Oil 50 ML
Himgange Ayurvedic Oil 100 ML
Himgange Ayurvedic Oil 200 ML
Himgange Ayurvedic Oil 500 ML
Himgange Amla Lite Oil 2.5 ML
Himgange Amla Lite Oil 29 ML
Himgange Amla Lite Oil 50 ML
Himgange Amla Lite Oil 100 ML
Himgange Amla Lite Oil 200 ML
Himgange Amla Lite Oil 500 ML
Himgange Jasmine Lite Oil 2.5 ML
Himgange Jasmine Lite Oil 29 ML
Himgange Jasmine Lite Oil 50 ML
Himgange Jasmine Lite Oil 100 ML
Himgange Jasmine Lite Oil 200 ML
Himgange Jasmine Lite Oil 500 ML
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G.K Burman Herbal (India) Private Limited is a "GMP (Good Manufacturing Practice) Certified" company. This certificate is given by Government of Uttarakhand to our company.

"GMP" or "Good Manufacturing Practice" are practices and the systems required to be adapted in pharmaceutical manufacturing, quality control, quality system covering the manufacture and testing of pharmaceuticals or drugs including active pharmaceutical ingredients, diagnostics, foods, pharmaceutical products, and medical devices. GMPs are guidance that outline the aspects of production and testing that can impact the quality of a product. Many countries have legislated that pharmaceutical and medical device companies must follow GMP procedures, and have created their own GMP guidelines that correspond with their legislation, basic concepts of all these guidelines remains more or less similar that is ultimate goal to safeguard the health of the patient, producing a good quality medicine or medical devices or active pharmaceutical products.

All guidelines follow a few basic principles given below:
  • Manufacturing processes are clearly defined and controlled. All critical processes are validated to ensure consistency and compliance with specifications.
  • Manufacturing processes are controlled, and any changes to the process are evaluated. Changes that have an impact on the quality of the drug are validated as necessary.
  • Instructions and procedures are written in clear and unambiguous language. (Good Documentation Practices)
  • Operators are trained to carry out and document procedures.
  • Records are made, manually or by instruments, during manufacture that demonstrate that all the steps required by the defined procedures and instructions were in fact taken and that the quantity and quality of the drug was as expected. Deviations are investigated and documented.
  • Records of manufacture (including distribution) that enable the complete history of a batch to be traced are retained in a comprehensible and accessible form.
  • The distribution of the drugs minimizes any risk to their quality.
  • A system is available for recalling any batch of drug from sale or supply.
  • Complaints about marketed drugs are examined, the causes of quality defects are investigated, and appropriate measures are taken with respect to the defective drugs and to prevent recurrence.
GMP guidelines are not prescriptive instructions on how to manufacture products. They are a series of general principles that must be observed during manufacturing. When a company is setting up its quality program and manufacturing process, there may be many ways it can fulfill GMP requirements. It is the company's responsibility to determine the most effective and efficient quality process.