Pharmanza Herbal
Clinical Research
Pharmanza Herbal conducts clinical trials following a rigorous process to ensure the safety and efficacy of the products. These trials involve multiple phases. In the initial phase, the company designs a detailed protocol outlining the study objectives, participant criteria, and methodologies. Subsequently, the herbal formulations undergo preclinical testing to assess their safety and potential effects.
We ensure ethical standards by obtaining informed consent from participants and maintaining transparency throughout the trial. The company collaborates with healthcare professionals, adheres to Good Clinical Practice guidelines, and submits comprehensive data to regulatory authorities for approval. The culmination of these phases contributes to the overall understanding of the herbal product’s safety and efficacy, supporting its potential release into the market.
Pharmanza Herbal is also engaged in pharmacokinetic studies by designing a protocol that outlines the specifics of the study, including drug testing, the study population, the dose regimen, and the sample schedule. They then administer the drug to participants, collect blood or urine samples at specified intervals, and analyse the samples to determine the drug’s concentration over time. The data collected are used to assess the drug’s absorption, distribution, metabolism, and excretion in the body. This process helps in understanding how the body processes the herbal product and guides decisions on dosage and administration.