VIMTA is the most reputed and No.1 choice in India for excellent quality clinical research services to Pharma, Biotech and Life-Science Industries. Our success is driven by our commitment to support customers win, through thorough understanding of the critical importance of time, technical on-time support, ethical care to subject safety, effective project management and strong GCP & GLP compliance.
We have rich experience, vast knowledge, advanced technologies and IT powered processes to conduct clinical studies. With strong local know-how and more than two decades of international regulatory experience VIMTA is your right partner for conducting clinical research studies in India.
Our expertise and leadership in Bioequivalence and Bioanalytical (BA/BE) Studies over the years has been extended to offer wider range of clinical research services such as clinical end point studies, claim studies for cosmetics and consumer care products, and clinical studies for complex neutraceuticals.
Regulatory Audits
Our Clinical and Bioanalytical sites are approved by CDSCO, Government of India
We have a very successful regulatory audit track record and have faced several regulatory audits from:
Services
With 23 years of experience and expertise, enriched through conduct of over 1700 studies, development of ~350 bioanalytical methods, and long track record of successful global regulatory audits from national and international regulatory authorities, we can help you design and conduct a study successfully in most time efficient and cost effective manner. Our strength lies in our ~100 member team of highly ethical, experienced, knowledgeable, multi-disciplinary, and customer focused professionals.
Clinic
Bioanalytical
Biostatistics and Data Management (BSDM)
VIMTA is committed to enhance data quality through best data management support systems and an integrated approach to prepare eCTD and CDISC implementation for smooth regulatory submission procedures. Our BSDM services and activities include:
VIMTA has experience in conducting investigative clinical studies, microbiological and invitro studies to verify and confirm product safety and efficacy on a wide range of consumer care, healthcare, food and cosmetics products.
Antimicrobial products - Efficacy testing of topical antimicrobials is conducted on healthy human subjects. Our experience includes, but not limited to:
Microbiology & In-Vitro Laboratory Testing
VIMTA is a full service, integrated Clinical Trials services provider offering Phases II, III, and IV studies. Ethics, subject safety and compliance to guidelines are a priority for VIMTA’s experienced scientific team.
We have strong PAN India network of 1500 GCP trained investigators, across varied therapeutic areas, and in-house expertise of clinical study management to conduct clinical trials.
We also offer exclusive or clinical trial integrated central lab services.
An exclusive lab is established with modern technologies to develop and offer bioanalytical methods for biosimilars including mAbs.
SERVICES:
Therapeutic Area Experience
VIMTA is a one-stop-shop for comparative or equivalence studies with respect to pharma, biotech or nutraceuticals products.
In addition to
We offer reliable and affordable Clinical End Point testing, where our experts from medical and scientific backgrounds can evaluate the clinical effect in the chosen population as per the protocol and submit a report in compliance to applicable regulations.
VIMTA has gained experience in offering clinical end point studies with:
We offer quality and cost-effective services to conduct claim studies for Nutraceutical products. Basically a nutraceutical is any substance that is a food or a part of food and provides medical or health benefits, including the prevention and treatment of disease.
Nutraceutical claim studies are performed as per applicable regulatory considerations. Pharmacokinetic and / or pharmacodynamic comparative studies are performed to support customers with the data that will help them to standardize / develop their product or to substantiate the product’s therapeutic claims.
Few products that have been evaluated against label claim:
VIMTA’s Central Lab is experienced in supporting long term & multi-centre Clinical Trials. A very wide range of services are offered including:
VIMTA is a pioneer in India, in Therapeutic Drug Monitoring using LC-MS / MS for Cyclosporine, Tacrolimus, Sirolimus
Key Features of Lab
Technologies
Central Lab Accreditations
