Haryana, India
WeensyBio Pvt. Ltd. is dedicated to advancing innovation in biotechnology, pharmaceutical sciences, healthcare, and nanotechnology through high-quality research and development services.
We provide scientific solutions ranging from proof-of-concept studies to advanced preclinical evaluation, enabling researchers and industries to accelerate innovation and commercialization.
We are a multidisciplinary Innovation-Driven Contract Research Organization (ICRO) — lean, accountable, and built around direct expertise. Our team spans molecular biology, nanobiotechnology, pharmacology, toxicology, and translational sciences, serving academia, startups, biotechnology companies, pharmaceutical industries, and government-funded research organizations.
We operate with the agility of a startup and the precision of an institution — delivering results that are accurate, reproducible, and regulatory-ready.
When you submit a sample, it goes directly to a senior scientist — not a technician, not a coordinator. The person running your analysis is the same person who interprets and signs the report.
All our analytical methods are internally validated against CDSCO, FSSAI, BIS, and relevant international standards. We never shortcut method development — your results have to hold up under scrutiny.
Pharma, food, agri, electronics — most labs specialise in one. We cover all four. If your product crosses categories, we already understand the full regulatory landscape.
Our reports are written for both scientists and business decision-makers. Clear conclusions, pass/fail summaries, and actionable next steps — no impenetrable jargon.
Standard delivery is 5–7 working days. We quote realistic timelines and we hold to them. If something changes, you hear from us first — not when the deadline passes.
Every deliverable is structured to meet submission requirements for FSSAI, CDSCO, and BIS. Our clients submit with confidence the first time because the documentation is built right from the start.
We treat every project as a scientific problem that deserves a clean, well-documented answer. No assumptions, no shortcuts. The work is methodical and the communication is direct.
You tell us what you need. We assess the sample type, required tests, and applicable regulatory standards — then provide a clear scope and quote within 24 hours.
Samples are logged into our tracking system on arrival. You receive confirmation and a projected delivery date. Everything is traceable from day one.
Testing is conducted using validated methods on calibrated instrumentation. Every run includes appropriate controls and standards. No data is ever adjusted post-analysis.
The final report is reviewed by a second scientist before release. You receive the report with a plain-language summary, raw data, and a clear pass/fail assessment.
Questions about the findings? Our scientists are available to walk you through the data directly — no account manager in between.