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Product Development Brief - Detailed
You’re one successful launch away from removing months of guesswork, compliance risk, and costly reformulations. Introducing the LULUBLE Comprehensive Product Development Template — the only development blueprint you’ll need for topical cosmetics, OTCs, and medical devices, designed and proven by an industry leader who’s developed and launched over 1,000 topical products.
Why this template matters
Built from real-world wins: Each section reflects processes, checklists, and documentation used to bring hundreds of formulations to market across cosmetics, over‑the‑counter actives, and regulatory-classified topical devices.
Prevent costly errors: Avoid formulation instability, label and claim rework, and regulator pushback by following pre-validated pathways aligned with the global best practices.
Save time and resources: Shorten development cycles with a repeatable, modular framework that guides teams from concept to commercial readiness — formulations, testing, QC, documentation, scaling, and launch.
What’s inside (high-level)
Product Brief and Market Fit: Target consumer profiles, competitive landscape, positioning statements, and claim architecture tailored to cosmetics, OTCs, and medical devices.
Regulatory Roadmaps: Decision trees for product classification (cosmetic vs OTC vs device), required documentation (510(k) considerations, NDAs, monographs), labeling requirements, permissible claims, and adverse-event reporting protocols.
Formulation Blueprints: Stepwise templates for emulsion, anhydrous, gel, ointment, and surfactant-based systems; ingredient selection criteria; compatibility matrices; preservative strategies; and stability risk assessments.
Analytical & Stability Testing Plans: Test matrices by product class (microbiology, pH, rheology, assay, preservative efficacy tests), stability protocol templates (conditions, timepoints, acceptance criteria), and shelf-life justification templates.
Safety & Clinical Pathways: Toxicology screening checklists, IRB-ready study templates, clinical protocol outlines for safety/efficacy trials, and adverse event/complaint handling workflows.
Quality Systems & Documentation: Master Batch Records, SOPs to satisfy partners and regulators.
Commercial Launch Kit: Claims substantiation checklist, packaging compatibility tests, retailer and distributor onboarding templates, and a post-market surveillance plan.
Who benefits
R&D teams looking to professionalize processes and reduce time-to-market.
Founders and innovators launching their first branded topical product.
Contract manufacturers and formulation consultants needing standardized, audit-ready deliverables.
QC managers who want a repeatable documentation system.
What sets LULUBLE’s template apart
Practitioner-proven: Authored by a developer responsible for 1,000+ topical launches — not an academic exercise. Every checklist and template has been used in regulatory submissions and commercial rollouts.
Cross-category versatility: Single framework that adapts to cosmetics, OTCs, and medical devices, eliminating the need for multiple disparate templates.
Actionable, not theoretical: Ready-to-use document modules, editable forms, and clear next-step guidance so teams can implement immediately.
Offer and next steps
Includes: Editable master template package (Word, Excel), example completed dossiers for a cosmetic, an OTC topical, and a medical device topical; three implementation checklists.
If you develop, manufacture, or plan to launch topical products, this template converts experience into repeatable success — minimizing regulatory friction, reducing reformulation risk, and accelerating revenue. Request the sample pack and a tailored onboarding call to start launching with confidence.
You’re one successful launch away from removing months of guesswork, compliance risk, and costly reformulations. Introducing the LULUBLE Comprehensive Product Development Template — the only development blueprint you’ll need for topical cosmetics, OTCs, and medical devices, designed and proven by an industry leader who’s developed and launched over 1,000 topical products.
Why this template matters
Built from real-world wins: Each section reflects processes, checklists, and documentation used to bring hundreds of formulations to market across cosmetics, over‑the‑counter actives, and regulatory-classified topical devices.
Prevent costly errors: Avoid formulation instability, label and claim rework, and regulator pushback by following pre-validated pathways aligned with the global best practices.
Save time and resources: Shorten development cycles with a repeatable, modular framework that guides teams from concept to commercial readiness — formulations, testing, QC, documentation, scaling, and launch.
What’s inside (high-level)
Product Brief and Market Fit: Target consumer profiles, competitive landscape, positioning statements, and claim architecture tailored to cosmetics, OTCs, and medical devices.
Regulatory Roadmaps: Decision trees for product classification (cosmetic vs OTC vs device), required documentation (510(k) considerations, NDAs, monographs), labeling requirements, permissible claims, and adverse-event reporting protocols.
Formulation Blueprints: Stepwise templates for emulsion, anhydrous, gel, ointment, and surfactant-based systems; ingredient selection criteria; compatibility matrices; preservative strategies; and stability risk assessments.
Analytical & Stability Testing Plans: Test matrices by product class (microbiology, pH, rheology, assay, preservative efficacy tests), stability protocol templates (conditions, timepoints, acceptance criteria), and shelf-life justification templates.
Safety & Clinical Pathways: Toxicology screening checklists, IRB-ready study templates, clinical protocol outlines for safety/efficacy trials, and adverse event/complaint handling workflows.
Quality Systems & Documentation: Master Batch Records, SOPs to satisfy partners and regulators.
Commercial Launch Kit: Claims substantiation checklist, packaging compatibility tests, retailer and distributor onboarding templates, and a post-market surveillance plan.
Who benefits
R&D teams looking to professionalize processes and reduce time-to-market.
Founders and innovators launching their first branded topical product.
Contract manufacturers and formulation consultants needing standardized, audit-ready deliverables.
QC managers who want a repeatable documentation system.
What sets LULUBLE’s template apart
Practitioner-proven: Authored by a developer responsible for 1,000+ topical launches — not an academic exercise. Every checklist and template has been used in regulatory submissions and commercial rollouts.
Cross-category versatility: Single framework that adapts to cosmetics, OTCs, and medical devices, eliminating the need for multiple disparate templates.
Actionable, not theoretical: Ready-to-use document modules, editable forms, and clear next-step guidance so teams can implement immediately.
Offer and next steps
Includes: Editable master template package (Word, Excel), example completed dossiers for a cosmetic, an OTC topical, and a medical device topical; three implementation checklists.
If you develop, manufacture, or plan to launch topical products, this template converts experience into repeatable success — minimizing regulatory friction, reducing reformulation risk, and accelerating revenue. Request the sample pack and a tailored onboarding call to start launching with confidence.