Our services
End-to-end agrochemical regulatory services
From a first feasibility check to a granted certificate and the licences that keep it usable, Pransh Pesticides Advisory handles the full regulatory lifecycle for pesticides, bio-pesticides and agrochemicals in India — for domestic manufacturers, importers and exporters alike.
- Registration across all Section 9 routes and product categories
- Import registration, permits and source documentation
- Export registration and destination-market support
- Data-gap analysis, study monitoring and dossier compilation
At a glance
What this covers
Pransh Pesticides Advisory provides complete CIB&RC regulatory services under the Insecticides Act, 1968 — product registration in every category, import and export registration support, data-gap analysis, study placement and monitoring, dossier preparation, Secretariat liaison, query handling, and post-approval licensing and lifecycle work.
Core services
Regulatory services, end to end
Each service is built around the same principle: settle the route and close the data gaps before spending, so every study earns its place in the file.
Product registration
CIB&RC registration across Sections 9(3B), 9(3) and 9(4) for insecticides, herbicides, fungicides, rodenticides, PGRs, bio-pesticides and antibiotics.
Learn more →Import services
Technical and formulation import registration, import permits, and foreign-manufacturer documentation for companies bringing products into India.
Learn more →Export services
Export-oriented registration and documentation for products manufactured in India for overseas markets.
Learn more →Data-gap analysis
A written, costed comparison of the data you hold against what the Rules require, with a realistic timeline — before any study is commissioned.
Learn more →Study placement & monitoring
Chemistry, bio-efficacy, toxicology, ecotoxicology, residue and shelf-life studies placed with recognised institutions and tracked to protocol.
Learn more →Licensing & lifecycle
State manufacturing and sale licences, endorsements, transfers, label additions and shelf-life changes that keep a registration usable.
Learn more →How we work
A single, sequenced process
Feasibility & route selection
We confirm the section and category, and check the active against the Schedule and the banned and restricted lists, before anything is commissioned.
Written data-gap analysis
A document that names the gaps, prices them and puts a realistic date on the certificate — so you decide with full costs in front of you.
Studies & dossier
Only the necessary studies, placed with recognised institutions, assembled into an internally consistent dossier in the prescribed format.
Filing, queries & grant
Submission, agenda tracking, deficiency replies answered with data, and follow-through to the certificate in Form II — then the licences to use it.
Answers
Services, answered
What services does Pransh Pesticides Advisory provide?
Complete CIB&RC regulatory services: product registration across all Section 9 routes and categories, import registration and permits, export registration support, data-gap analysis, study placement and monitoring, dossier compilation, Secretariat liaison, query handling, and post-approval licensing and lifecycle work.
Do you handle both import and domestic manufacture?
Yes. We support importers registering technicals and formulations (TI and FI categories) as well as domestic manufacturers under the indigenous-manufacture categories (TIM and FIM), and we align central registration with the state licences needed to actually manufacture and sell.
Can you help a company that only wants to export from India?
Yes. Products manufactured in India purely for export follow a distinct export-oriented registration path. We confirm eligibility, keep the data proportionate to that route, and prepare the documentation destination markets expect.
Where are you located?
Our office is at SCO 79, Second Floor, Omaxe World Street, Sector 79, Faridabad, Haryana 121004 — the same region as the CIB&RC Secretariat, which keeps submissions and follow-ups fast.
Let's begin
Talk to a CIB&RC registration consultant
Tell us the molecule, the formulation and the route you have in mind. We will confirm the applicable section, the data you already hold, and what is missing — before you spend on studies.