Featured Service
Fast, Reliable Gene‑to‑Clinic Development
Bring your biologic program to life with an end‑to‑end CRADS platform
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Accredited by
- NABL
- ISO 17025
- GLP
- GMP
- OECD
- WHO-GMP
- FSSAI
- DSIR
- BIS
Capabilities by industry
Drug Discovery & Development
End-to-end testing across the drug-development lifecycle — discovery, preclinical, clinical, cGMP analytical and biologics. The practice that built Vimta, audited by every major submission market we file in.
Focus Areas
Regulatory
- USFDA
- EMA
- MHRA
- ANVISA
- PMDA
- CDSCO
- OECD GLP
Food & Personal Care
Nutritional analysis, pesticide residue, contaminant testing and FMCG product safety — covering FSSAI, EU MRLs, and every major export market.
Regulatory
- FSSAI
- AOAC
- EU MRLs
- BIS
- NABL
Electricals & Electronics
EMI/EMC, safety, environmental and certification testing across seven product domains — including avionics and defence electronics.
Focus Areas
Regulatory
- BIS
- CE
- FCC
- IEC
- NABL
- MIL-STD
Environment, Health & Safety
Ambient, stack, water, soil and waste analytics for EIAs, post-project monitoring and CPCB-mandated submissions.
Regulatory
- MoEF
- CPCB
- NABL
- ISO 17025
- EIA
Crop Care & Specialty Chemicals
Contract research and regulatory studies for agrochemicals and specialty chemicals — registration, efficacy and residue work under GLP.
Focus Areas
Regulatory
- CIBRC
- OECD GLP
- USEPA
- EU REACH
- NABL
Choose an industry
Featured Services
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Analytical Services for Preclinical
The analytical services play a crucial role in drug development journey by providing evidence based data about various parameters in accordance with the regulatory…
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EMI and EMC Testing
We have our customers covered with a wide range of test facilities that will allow customers to test as per requirements of various regulatory…
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Safety and Performance Testing
With constantly evolving regulations and technology improvements, manufacturers are faced with a constant challenge to keep up with the regulatory and safety standards of…
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Active Ingredients/Markers (Nutraceuticals)
The active ingredients are specific compounds that are capable of demonstrating therapeutic or biochemical effects. At VIMTA, we offer complete range of testing services…
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Phase-I & BA/BE Studies
Bioequivalence / Bioavailability studies popularly known as BA/BE studies are key requirement by regulators to ensure comparability between a pharmaceutically comparable test item and…
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Early Drug Discovery & Development
In the early stages of development, gathering reliable information with a quick response time is of paramount importance. VIMTA offers a complete range of…
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General Toxicity
VIMTA offers a complete range of standard toxicology studies designed for supporting submissions to various regulatory agencies. Equipped with multiple test species including Beagle…
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Toxicological Risk Assessments
Since we are exposed to a large number of chemicals daily, either directly or indirectly, it is important to evaluate the toxicity of individual…
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BIS CRS Testing
Bureau of Indian Standards grants license to the manufacturers to use or apply Standard Mark with unique R-number, through registration based on self-declaration of…
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CE Marking Certification and Testing
The letters CE are abbreviation for French phrase “Conformité Européenne“ which means “European Conformity” in English. This is a common regulatory scheme to gain…
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TEC Testing
TEC, under Department of Telecommunications (DoT), announced the procedure for Mandatory Testing and Certification of Telecommunication Equipment. Such testing shall be carried out by…
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Agmark Grading
AGMARK is a certification mark for agricultural products in India, which assures that the products conform to defined standards known as AGMARK standards. These…
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About Vimta Labs
A Pioneer in Scientific Excellence Since 1984
Founded in Hyderabad in 1984, Vimta Labs has grown into one of India's foremost Contract Research & Testing Organization — serving 30,000+ clients across pharma, food, environment, and electronics from state-of-the-art facilities spanning 6 lakh sq ft.
Sq. Ft. of Ultra-Modern Lab Space
Customers
External Audits Annually
Countries Served Globally
Insights Hub
Thinking That Drives Progress
Research, events, case studies and careers from Vimta's scientists and regulatory experts.
The revised ICH M10 reshapes how sponsors validate bioanalytical methods for regulatory submissions. Here's what CROs — and their sponsor partners — need to adjust in 2026.
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Why CMC Readiness Makes or Breaks Your IND Filing
CMC gaps remain the leading cause of FDA clinical hold letters. We break down the five most common CMC red flags we see from first-time IND sponsors.
Sponsor needed bioanalytical method validation and TK sample analysis completed in under 12 weeks to meet IND submission window.
OEM needed BIS, EMI/EMC, and product safety testing for a connected-appliance line targeting launch across four South Asian markets.
Exporter needed EU MRL-compliant multi-residue testing on 120+ SKUs with three-day turnaround to hold shipping commitments.
About this role As a Senior Scientist — Bioanalytical (LC-MS/MS), you will partner with cross-functional teams to deliver measurable impact within the Vimta scientific ecosystem. This role blends hands-on execution…
Open Role
About this role As a Group Leader — Clinical Operations, you will partner with cross-functional teams to deliver measurable impact within the Vimta scientific ecosystem. This role blends hands-on execution…
Open Role
About this role As an Analyst — Food & Water Testing, you will partner with cross-functional teams to deliver measurable impact within the Vimta scientific ecosystem. This role blends hands-on…
FAQ
Frequently Asked Questions
Quick answers to the questions we hear most often from our clients and partners.
Vimta provides end-to-end contract testing and research across five sectors: pharma & biopharma (bioanalytical, clinical, CMC, stability, drug discovery support), food & personal care, electricals & electronics (EMI/EMC, safety, performance), environment health & safety, and crop care & specialty chemicals. Services span method development, regulatory testing, GLP/GMP studies, and product certification — all delivered from our NABL- and GLP-accredited facilities in Hyderabad.
Our labs operate under NABL (ISO/IEC 17025), GLP (OECD principles), USFDA inspections, WHO-GMP, CDSCO, FSSAI, BIS, and DSIR, among 30+ international accreditations. Reports issued by Vimta are accepted by regulators in the US, EU, Japan, and across Asia-Pacific, so sponsors can file submissions globally without redundant re-testing.
Share your study outline or sample details through our Contact form, email enquiry@vimta.com, or call the Hyderabad facility directly. Our project management team typically reaches out within one business day with a scoped quote, turnaround estimate, and shipping instructions. For regulated-study sponsors we also sign CDAs upfront.
Turnaround depends on matrix, method status, and regulatory scope. Routine analytical testing is usually 5–10 business days; validated bioanalytical sample analysis runs on scheduled batches with study-specific timelines; GLP toxicology and stability studies follow protocol-defined durations. Every quote includes a concrete timeline and milestone plan so you can align internal submissions.
Yes. Every engagement starts with a mutual CDA, followed by a study-specific contract covering data ownership, retention, and audit rights. Study data is held in 21 CFR Part 11–compliant systems with role-based access, and our QA unit archives raw data under GLP/GCP record-keeping rules. Sponsor representatives can audit studies on-site or remotely by prior arrangement.
Get in touch
Let's discuss your testing needs
Whether you need a single test or a full-scale contract research programme, our team is ready to scope the right solution for you.
Registered Office & Central Lab
Address: 142, IDA, Phase II, Cherlapally Hyderabad – 500 051 India.Phone: +91 40 2726 4141, +91 40 2726 4444, +91 40 27268100
Fax: +91 40 2726 3657
Email: bd@vimta.com
Life Sciences Campus
Address: #5, Neovantage Innovation Parks, Genome Valley, Shameerpet, Hyderabad – 500101, Telangana, India.Phone: +91 40 6740 4040
Fax: +91 40 6740 4401
Email: bd@vimta.com
Send us an enquiry
Tell us about your testing or research needs and we'll scope the right solution.
Careers at Vimta
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Join 1,500+ scientists, engineers, and analysts solving real problems for pharma, food, and electronics companies across the world.