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I’m launching a health-improvement nutraceutical line and require deep, hands-on help shaping the very first product. The core of the assignment is threefold: create a robust, evidence-based formulation, ensure every step aligns with current FSSAI standards, and benchmark our ingredient mix against top Indian and global competitors so we enter the market with a clear edge. What I already have: • A broad concept of the benefit profile I want (overall health improvement). • Early notes on possible botanicals and bio-actives. What I need from you: – Translate that concept into a finished formula with substantiated active levels. – Pull and summarise peer-reviewed clinical data that supports each selected ingredient. – Validate dosage ranges for both efficacy and safety, flagging any contraindications. – Build the full FSSAI compliance dossier: permissible RDA limits, additive status, safety certificates, and label claim wording that can stand up to scrutiny. – Compare at least five leading SKUs for ingredient choice, concentration, pricing per daily dose, and USPs, then pinpoint positioning gaps we can exploit. – Recommend vetted raw-material vendors (India or abroad) with quality documentation in place. Deliverables will include: 1. Formulation sheet (Excel/Sheets) with actives, excipients, dosages, and rationales. 2. Clinical evidence compendium (PDF) organised by ingredient. 3. FSSAI compliance checklist and draft front-/back-panel label text. 4. Competitor benchmarking report with visual charts. 5. Short-list of raw material suppliers and spec sheets. Acceptance criteria: • All actives must fall within FSSAI stipulated limits. • Minimum two peer-reviewed studies per active demonstrating health-improvement outcomes. • Benchmarking must cover at least 90 % of market share leaders in the chosen category. Please outline your relevant formulation projects and typical turnaround times so we can map a realistic timeline and milestone plan.
ID Projek: 40270057
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Hi thanks for the detailed brief. Your project combines three key areas: evidence-based formulation, FSSAI compliance, and competitive benchmarking, and I’m well positioned to coordinate this kind of work. My role is to manage the full development process from concept to production-ready documentation. For a project like this, the typical timeline is about 4–5 weeks, structured in phases: • Market & competitor benchmarking • Evidence-based formulation with validated dosage ranges • Clinical research compilation • FSSAI compliance review and label guidance • Supplier shortlisting I’ll make sure you get a highly qualified specialist formulator involved where needed, while I oversee the research, documentation, and deliverables so everything stays aligned with your launch goals. If helpful, I can also outline a quick milestone plan for the deliverables you listed.
₹25,000 INR dalam 7 hari
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Hyderabad, India
Ahli sejak Mac 2, 2026
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₹12500-37500 INR
₹12500-37500 INR
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$2-8 AUD / jam
$10 USD
₹750-1250 INR / jam
₹12500-37500 INR
₹750-1250 INR / jam
$5000-10000 USD
₹750-1250 INR / jam
$30-250 USD
₹10000-10001 INR
$2-8 USD / jam
$500-2000 USD
$500-1500 USD