The core competencies of Lotus Labs are perfectly amalgamated with global regulatory standards for Phase I to IV clinical trials including human bioavailability, bio equivalence, first in man, food effect, special population & other pharmacokinetic studies, drug storage & distribution, bio-analytical and statistical services.

Our clinical and bio-analytical facilities and processes are inspected by the Drugs Controller General of India (DCGI), US FDA, AFSSPS (France), WHO, AGES (Austria), ANVISA (Brazil), MCC (South Africa), MOH (Turkey) and MCC (Zimbabwe), assuring our clients of the best quality practices and procedures.

At Lotus Labs, we plan, develop and execute time-bound projects with a team of qualified scientists, who specialize in various disciplines. Our teams are constantly working towards upgrading clinical and bio-analytical competencies that are tuned to meet customer requirements.

A dedicated Training department ensures that all technical personnel at Lotus Labs are trained and constantly updated with all relevant procedures and techniques. This has ensured that we deliver quality in every facet, time and again.

Professional excellence, ethical frameworks and sound technical knowledge are the hallmarks of every service from Lotus Labs.