Quality and safety are the fundamental principles of Ayurvedic medicine preparation. Every batch is closely monitored — from raw material to final product — ensuring efficacy, safety and zero toxicity.
Quality and safety is a fundamental principle of preparation of Ayurvedic medicines for health care. It is also a very important step for quality control. Since the drug is to be applied to the human body, it must be of good quality and should be closely monitored to ensure that it does not produce any harmful effects after its application.
Medicinal scientists have repeatedly emphasized the medicinal properties. It is the ethical responsibility of every manufacturing organization to consider the efficacy, safety and non-toxicity of medicines.
Every Ayurvedic preparation under Dr. Dulal's supervision passes through four rigorous stages of quality control — from clear scientific definition to active constituent assay.
Quality testing must begin with a clear scientific definition of raw materials. The exact species, usable plant part, origin, collection period, harvest time and drying method must all be precisely documented. Even the soil specifications are defined.
For accurate identification of raw material components, multiple verification methods are applied — visual examination, taste, smell, macroscopic, microscopic and organoleptic properties, plus chromatographic analysis. Comparisons can be conducted for further certainty.
Comprehensive analysis evaluates the quality of herbal raw material — moisture content, ash value, extraction value, microbial contamination, heavy metals, pesticide residue and aflatoxin testing. Only materials passing all tests proceed to manufacturing.
Determination of constituents with known therapeutic activity — and their quantitative measurement — is essential. Where chromatographic methods are not suitable, biological assay of active constituents may be performed for accurate potency confirmation.
"It is the ethical responsibility of every manufacturing organization to consider the efficacy, safety and non-toxicity of medicines."
— Dr. Shahinoor Rahman Dulal
Every product follows a five-stage quality assurance process — from sourcing through final release.
Dr. Dulal has established quality control SOPs at over 80+ pharmaceutical organisations across South Asia and Turkey — bringing 20+ years of expertise to every batch.