As we have seen in Chikitsa Padah, the medicine’s role is crucial in the success of a treatment.
We work with only old, proven, trusted and renowned companies and people having a thorough understanding of Ayurveda, a profound respect for the herbs and plants and mastering the art of collecting it and preparing it so that their potential is maximum.
Many herbs are only available in regions that are hard to reach or are becoming rare due to their over extensive usage, or also improperly prepared and collected so that their potency is less efficient. All that is taken in account when choosing a medicine as herb safeguard is a major deal for our future.
We use different kind of preparations and formulations such as Churna ( powders ), tablets, capsules, Asavas and Arishtas ( alcoholic preparations ), Ghee and tailam ( oil ) preparations, sometimes processed with specific decoctions, milk, meat or cow urine and buried in the ground for months,etc.
Mainly, the medicine are herbal compounds but for specific and very advanced diseases, an herbo-mineral medicine can be advised or required. First, it is important to know how minerals work in the body. This is something that modern science has no tool to understand or prove. Minerals undergo a purification process in order to make them bioavailable. This word is key to apprehend how it will effectively work in the body.
As no disease and no person is the same, this uniqueness creates a wide variety of medicine that only a wise and experimented Doctor will be able to select accordingly.
Currently, we are proudly working with companies in India that are sharing our ethic, transparency and vision. Among them are:
Checks and accreditation
– WHO GMP
Good manufacturing practice (GMP) is that part of quality assurance which ensures that products are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the marketing authorization. GMP is aimed primarily at diminishing the risks inherent in any pharmaceutical production, which may broadly be categorized in two groups: cross contamination/mix-ups and false labelling. Above all, manufacturers must not place patients at risk due to inadequate safety, quality or efficacy; for this reason, risk assessment has come to play an important role in WHO quality assurance guidelines.
The Department of Scientific and Industrial Research (DSIR) is a part of the Ministry of Science and Technology, which was announced through a Presidential Notification, dated January 4, 1985 (74/2/1/8 Cab.) contained in the 164th Amendment of the Government of India (Allocation of Business) Rules, 1961. The Department of Scientific and Industrial Research (DSIR) has a mandate to carry out the activities relating to indigenous technology promotion, development, utilization and transfer. It also oversees the Council of Scientific and Industrial Research (CSIR), India’s largest research and development organization.
ISO is an independent, non-governmental international organization with a membership of 163 national standards bodies. Through its members, it brings together experts to share knowledge and develop voluntary, consensus-based, market relevant International Standards that support innovation and provide solutions to global challenges.
Our Central Secretariat is based in Geneva, Switzerland. International Standards make things work. They give world-class specifications for products, services and systems, to ensure quality, safety and efficiency.
Pharmacopoeial Laboratory for Indian Medicine (PLIM) is a subordinate office of the Ministry of Health & Family Welfare, (Deptt. of AYUSH), Govt. of India.
This laboratory is a Standards Setting cum Drugs Testing Laboratory at National Level for Indian Medicines which include drugs of Ayurveda, Unani and Siddha systems.
The Committee for the Purpose of Control and Supervision of Experiments on Animals(CPCSEA) is a statutory Committee, which is established under Chapter 4, Section 15(1) of the Prevention of Cruelty to Animals Act 1960. India is one of the pioneering countries to institute Prevention of Cruelty to Animals Act in 1960 whereas such Act was instituted in France in 1963 and in USA in 1966. The detailed rules for experimentation on animals were first enacted by the Ministry of Agriculture in 1968 and were implemented by a Committee set up in pursuance of Section 15(1) of the PCA Act,1960.