About us
A regulatory consultancy built around manufacturing, not paperwork
Foodlinedocx Lifesciences Private Limited advises food, nutraceutical, cosmetics and pharmaceutical manufacturers on licensing, documentation and plant setup. We are based in Delhi and work with plants across India.
Who we are
Foodlinedocx was set up to do one thing properly: get manufacturing projects in the food and lifesciences sector licensed, and keep them compliant afterwards. The founding team has spent more than a decade in regulatory work across pharma and food, with the deepest experience in setting up nutraceutical and health supplement manufacturing units, and has supported over a hundred such projects.
That background shapes how we work. We came to licensing through factories rather than through law, so we start with the plant: what it will make, how the material and people will move, what the air handling has to do, and what the officer inspecting it will want to see. The application form is the last step, not the first.
Most of what we are asked to fix is a sequencing problem. A building goes up, machinery is installed, and only then does somebody ask what the licence requires. By that point the change rooms are in the wrong place and the utility room blocks a material path. Running the regulatory workstream alongside construction costs less and finishes sooner, every time.
12+ years
Combined regulatory experience across food and pharma
100+
Nutraceutical and health supplement projects supported
Pan-India
Filings with FSSAI, CDSCO and state authorities
Delhi NCR
Based in Delhi, working with plants nationwide
How we operate
Four commitments we hold ourselves to
Regulatory consulting has a reputation problem, largely earned. These are the specific things we do differently, stated plainly enough that you can hold us to them.
We tell you what you do not need
A consultancy paid per licence has an incentive to sell you licences. We would rather tell you that one filing covers your requirement and keep the relationship, than sell you three and lose it.
Fixed scope, fixed fee
You get a written scope and a fixed professional fee before work starts. Government fees are payable directly to the authority, shown separately and never marked up.
We write the technical documents ourselves
FSMS plans, dossiers, SOPs and layouts are drafted by our team from your actual process. Downloaded templates are the reason most files come back with queries.
No guarantees on outcomes
We do not promise that a regulator will approve anything, because nobody can. We take responsibility for file quality, response times and inspection readiness, which is what actually determines most outcomes.
Capabilities
What we cover
Four practice areas, deliberately narrow. Anything outside them we will tell you honestly is not our work.
Food and nutraceuticals
FSSAI Central and State licensing, registration, nutraceutical and health supplement approvals, FSMS and HACCP documentation, product and label compliance.
Cosmetics
Manufacturing and import licensing under the Cosmetics Rules, 2020, import registration with CDSCO, and Indian labelling compliance for imported ranges.
Pharmaceuticals and CDSCO
Classification opinions, drug manufacturing licences on Form 25 and Form 28, revised Schedule M readiness and inspection support.
Engineering and projects
Factory layouts, HVAC zoning, equipment specification, detailed project reports and turnkey plant setup coordination.
Start with a conversation, not a contract
Describe your project. If we are the right people for it we will tell you what it takes, and if we are not, we will say that too.