Contract Research Organization in India

Wide range cGMP compliant, large capacities, market leader in contract testing and analytical R&D services

1st laboratory in Asia to be pre-qualified by WHO for Medicines Programme Inspection of Quality Control Laboratory

Successfully audited by USFDA

1st Laboratory in India to offer Customer Specific Contract Laboratories

cGMP LABORATORY SERVICES

cGMP & Laboratory Services
Food safety evaluations for regulatory compliance

NABL Accredited, APEDA recognized, EIC Accredited, FSSAI notified

First lab in India to be approved by European Commission for Analysis of PCPs in Food Exports to Europe

PAN India network with state of the art laboratories

Analytical Food Water

Food & Water Testing
AAALAC accredited and GLP certified facility for leveraging global data acceptability

Multi therapeutic efficacy models and early ADMET screen for lead identification & lead optimization

Impurity qualification resources using insilico, invitro and invivo toxicology studies.

Biocompatibility evaluation for Medical Device and Packaging Materials

Innovative experimental approaches for drug repurposing program

Preclinical Research

Preclinical Research
Since 1995, one of the pioneering CRO in India

Expertise and leadership in Bioequivalence and bioanalysis services covering in-vivo/ in-vitro, healthy volunteers and patient studies.

Strong local know-how and international regulatory experience

Clinical Research

Clinical Research
Supporting development of Biosimilars, Industrial enzymes characterisation, genetic markers testing, Biomarkers identification, Biological assays

Partnering with industry, academia, research institutes & individual research scientist fraternity.

Biopharma

Biopharma
1st Environment Protection Act recognized Lab in India since 1986.

Accredited by QCI-NABET by providing Environmental Impact Assessment and Consultancy Services

Environmental Assessments

Environmental Assessments
ISO 15189 Accredited by NABL 15189 & CAP Accredited

Routine and specialized Clinical Reference diagnostic services

Central Lab Services to support clinical trials

Clinical Reference Lab

Clinical Reference Lab

Packaging Material Testing, USP 661.1, USP 661.2|Elemental analysis in raw material, drug substances and drug products as per ICH Q3D|Particle Size Analysis on Malvern Master sizer 3000|Water Testing as per US EPA and IS10500 standards|Extractables and Leachables studies for Pharmaceutical Packaging / Delivery Systems|Contraceptives testing as per ISO 4074: 2015|Comprehensive analytical testing services for Food Allergens.|Transgenic Crops Composition Testing as per requirements of ICMR guidelines-2012 |Impurity qualification studies for API & Drug Products|Medical devices testing as per ISO 10993 Characterization of Low Molecular Weight Heparin as per US-FDA and EMEA guidelines|Impurity qualification on Capillary Electrophoresis (CE).

New Services

LATEST EVENTS

SOT Annual Meeting and TOXEXPO 2020 | 15-19 March, 2020, Anaheim, CA, USA, booth number ( # 357 )

Upcoming Events

To be announced soon

VIMTA Corporate Video

Accreditations / Regulatory Audits / Licenses / Recognitions / Professional Associations

Registered Office & Central Lab
142, IDA, Phase II,
Cherlapally,
Hyderabad - 500051, India.
Tel : +91 40 2726 4141, +91 40 2726 4444
Fax : +91 40 2726 3657
Email : bd@vimta.com