Complete end-to-end solution to create and launch your own health product from market and scientific analysis to formulation, industrial process design, regulatory dossier preparation, and operational launch.
A complete end-to-end solution to create and launch your own health product - from market and scientific analysis to formulation, industrial process design, regulatory dossier preparation, sourcing, manufacturer agreement, branding, registration, and operational launch.
We deliver fully compliant, ready-to-market pharmaceutical, nutraceutical, and dermocosmetic products with end-to-end execution.
A complete end-to-end solution to create and launch your own health product - from market and scientific analysis to formulation, industrial process design, regulatory dossier preparation, sourcing, manufacturer agreement, branding, registration, and operational launch.
Food supplements and cosmetic products, with full alignment to applicable EU and local regulations. On request, SCPS can also support the development of medical devices and pharmaceutical products under adapted project frameworks.
A custom-developed product, fully registered in your target country, delivered EXW from Europe, and supported by scientific marketing assets - ready for immediate commercialization.
Available as a full 5-phase turnkey process or individual services depending on your needs.
A rigorous STOP/GO methodology ensures transparent decision-making at each phase, measurable deliverables, and no unnecessary costs.
Up to 350+ hours of internal work, shorten lead time by 3–6 months, secure full scientific support, optimized development & sourcing, and high-impact launch assets - all at a lower total cost.
From initial market analysis to product launch, we handle every step with precision and expertise. Our proven methodology reduces risks, accelerates time-to-market, and maximizes your ROI.
Every project follows a structured and transparent methodology divided into five phases.
Each phase ends with a STOP/GO validation checkpoint, allowing you to confirm decisions and manage risks with clarity and cost control.
Conduct in-depth market research, competitor and product mapping, and customer profiling to identify opportunities and define their optimal positioning – or to evaluate the positioning of a specific product concept already defined by the client.
Conduct scientific and clinical evaluations of the most relevant and innovative solutions targeting a specific therapeutic need, to determine expected efficacy, potential side effects, regulatory suitability, and comparative performance – or to assess the scientific relevance of a product concept already defined by the client.
Perform scientific and regulatory literature reviews to evaluate a suitable innovative combination of ingredients, synergies, and formulation strategies. Analyze existing compositions and clinical data to refine the evidence-based formula. Deliverables include a detailed formulation file with dosing rationale and technical specifications, building on Phase 1 outcomes.
Translate the target formulation into a suitable and cost-effective industrial process. Define the optimal galenic form, physical characteristics (density, viscosity, pH, etc.), and critical process parameters to ensure stability, bioavailability, and regulatory compliance. The goal is to align scientific performance with industrial feasibility and production simplicity.
Supervise pilot-scale manufacturing trials to produce first samples. Evaluate key quality attributes such as appearance, texture, and stability. Conduct preliminary lab testing to validate the formulation and identify necessary adjustments before moving to full-scale industrial production.
Compile the full technical file for registration in the target market, including formulation and scientific data, specifications, and manufacturing certifications. SCPS can also handle notifications in France or Europe through a licensed French pharmaceutical entity, while maintaining client ownership. This option enhances regulatory and marketing credibility, with potential for French co-branding to support market positioning.
When required, additional studies can be conducted to reinforce regulatory submissions or support marketing claims: clinical evaluation reports (CER), stability or toxicological studies, interaction or nutritional value reports, etc.
SCPS can secure scientific claims such as clinically proven, patented, dermatologically tested, or equivalent, either by leveraging existing data or coordinating dedicated studies and patent filings.
Secure and manage your transactions through a licensed French pharmaceutical entity.
Enhance your product's credibility by co-branding with a French R&D laboratory specialized in pharmaceutical and nutraceutical development reinforcing scientific positioning and trust with healthcare professionals and end-consumers.
Conduct on-site audits to assess technical quality, and regulatory compliance of manufacturers.
Provide in-person scientific & product training sessions tailored to your teams or clients.
Manage ongoing supplier relationships, including performance tracking and issue resolution.
Access specialized legal expertise for contract review, compliance validation, and risk mitigation.
Full shipping management to final destination, including customs clearance and logistics.
Support full technology transfer processes between manufacturers and target territory.
Identify and source potential manufacturers globally — with a focus on Europe — that meet the project's technical, regulatory, and operational specifications.
Conduct a comparative assessment of shortlisted manufacturers based on predefined criteria. Engage directly with selected sites to validate capabilities, compliance, and technical alignment with the product development strategy.
Develop a structured negotiation framework once a suitable manufacturer has been identified – defining the client's strategic preferences, constraints, target conditions, and partnership expectations.
Conduct the commercial negotiation process based on the predefined framework, leading detailed discussions with the manufacturer over several rounds to align on the core commercial, technical, and regulatory terms.
Prepare, structure, and negotiate the complete contractual package covering all relevant operational, quality, regulatory, commercial, and technical provisions – to secure a comprehensive, compliant and robust final agreement.
Create final brand identity, packaging artwork, and regulatory-compliant texts in multiple languages aligned with target market requirements.
Prepare and collect the complete registration dossier required in your country, ensuring accuracy and compliance.
Develop scientific marketing content tailored to the product and target market, ready to support medical, regulatory, and commercial teams.
Develop and deliver scientific and product training programs for sales teams and medical representatives, integrating pathology insights, product science, clinical evidence, and competitive differentiation to enhance field performance.
Oversee the full production and delivery cycle – coordinating manufacturing activities, quality milestones, logistics, customs documentation, and LC procedures to ensure a controlled and compliant EXW delivery.
Whether you're leading a small or mid-sized healthcare company or managing innovation within a larger group, you may have identified a market opportunity, a product idea, or a therapeutic need...
But turning that concept into a high-quality, compliant, and industrially viable health product requires time, coordination, and a broad set of scientific, regulatory, and manufacturing capabilities– all working together.
Choosing the wrong concept, the wrong formulation, missing critical regulatory constraints or working with an unqualified manufacturer can compromise the entire project.
Delays, underperforming products, excessive costs, or even failures to register are frequent consequences of fragmented execution.
Developing a pharmaceutical, nutraceutical, or dermocosmetic product involves risk and deserves the same rigor as a market launch.
SCPS offers a turnkey solution to design and develop your own health product from scratch and bring it to market faster, with less risk and cost.
We manage the full 5-phase process for you:
You retain control of your idea, we transform it into a compliant, ready-to-launch product with minimal operational burden.
Our teams handle the full upstream execution: R&D, formulation, industrial design, technical documentation, supplier engagement, scientific marketing and final delivery.
What could take your team 15–18 months and 350+ hours, we deliver in 9–12 months with under 20 hours of your involvement.
SCPS turns complexity into a streamlined, high-performance product development process.
You get a validated product, built with expert standards, ready for market — while staying focused on what matters most: your strategy, your brand, and your growth. You gain time, expertise, and full ownership of your product with the option to co-brand with a French laboratory for added scientific and marketing impact.
This scenario illustrates the kind of support SCPS can provide through a full-service development engagement:
A client planning to launch 30,000 units of a new healthcare product in Algeria entrusts SCPS with the complete upstream process from concept validation to industrial readiness and market registration.
With an investment starting from € 25,200, SCPS delivers, within 9 to 12 months:
Project efficiency and savings:
This case highlights SCPS's ability to deliver a fully developed, compliant, and market-ready product with scientific depth, operational control, and a clear return on investment for small and mid-sized companies.
Actual scope and pricing may vary depending on project configuration and target markets.
Let's discuss how we can help you develop and launch your own scientifically-supported health product from concept to market with minimal operational burden and maximum impact.
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