Directory:LotusLabs

MyWikiBiz, Author Your Legacy — Monday December 30, 2024
Revision as of 08:23, 15 March 2012 by Slater.jim001 (talk | contribs) (Created page with 'File:Lotuslabs.jpg Renewed threats from disease, fresh challenges from debilitating conditions and the scourge of pandemics demand rapid responses and concerted efforts on …')
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigationJump to search

Lotuslabs.jpg


Renewed threats from disease, fresh challenges from debilitating conditions and the scourge of pandemics demand rapid responses and concerted efforts on a global scale. Thus, when global pharmaceutical, biotechnology and medical device companies need to bring better drugs to the market faster, they need partners who can collaborate to ensure seamless development and delivery. The inherent merits of a large and diverse target pool for trials, regulatory and legal frameworks, world class infrastructure and a powerful IT and knowledge sector have ensured India’s emergence as an alliance and outsourcing destination of choice for global pharmaceutical majors across the value chain - with Clinical Research constituting a large and potent arena for partnerships.


With over 1,400 studies, development of validated Bio-analytical methods for over 230 molecules, and investigations being inspected and approved by various global regulatory authorities, Lotus Labs ranks high amongst the Clinical Research Organizations in India to take the lead in providing specialized services that are best-in-class in the domain of clinical research and within budget. As a Clinical Research Organization, our core competencies are in the realm of planning, designing and managing Clinical Trials -with clients that include national and international Pharmaceutical majors (innovators as well as generic pharmaceutical enterprises), Biotechnology and Medical Device organizations.


The capabilities at Lotus to conduct phase i studies at Lotus are backed by vast experience in clinical trials. Lotus offers the state-of-the-art infrastructure to conduct phase i studies in healthy volunteers. At Lotus Labs, our medical writing services ensure that all regulatory submission documents are clear, concise, scientifically as well as medically accurate & fully compliant with all applicable ICH and regulatory guidelines with submission reports provided in eCTD and CTD formats.


At Lotus Labs, the objective of heralding hope, the accent on nurturing excellence, the endeavor to ensure successful outcomes and the enduring belief in synergistic partnerships – are the building blocks of our DNA - a tenet that finds eloquent expression in our catchphrase.


Lotus Labs - Centre of Excellence for Clinical Research