Protocol development, data management, trial monitoring, data analysis and report writing

Consulting

In the domain of international GMP/GLP certification, Pharmaceutical Product development, Identification, propagation of depleting bio-resources and building robust supply chains for Herbal raw material.
BioMantra has an exceptional grasp of the intricate field of Clinical Trials that enables clients meet the most rigorous of Global Regulatory norms. In the context of Herbals and Traditional Medicine BioMantra builds protocols that are acceptable to Regulators around the world.
BioMantra has developed proprietary monitoring and data management tools that can be customized to the needs of each clinical trial and meet the standards and norms of regulators to ensure strict compliance with the targeted drug approval agency requirements in precisely those details that can lead to rejection of the trial results.
BioMantra’s expertise in the area of clinical trial statistical data analysis ensures that the results are analyzed in the most effective manner possible. Further, it can ensure that weaknesses in data generation are brought to the attention of the Investigation team early enough during the trial to enable them to generate additional data where required.
BioMantra has excellent skills in technical writing. BioMantra reports present the findings of the study in a manner that ensures full understanding of the results and fast approval of the product.