Complete operational solution to analyze, source, brand, register and deliver scientifically supported ready-to-market products with full preparation and sales team training.
We deliver fully compliant, ready-to-market pharmaceutical, nutraceutical, and dermocosmetic products with end-to-end execution.
A complete operational solution to analyze, source, brand, register and deliver scientifically supported ready-to-launch products with full preparation and sales team training.
Medical devices and supplements plus dermocosmetics – fully compliant with relevant European and local regulations. Pharmaceutical products can also be supported with a tailored process on request.
A product fully registered in your country, delivered EXW Europe with scientific marketing materials ready for commercialization.
Available as a full 4-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 200+ hours of internal work, 3–6 months lead time reduction, secure full scientific support, optimized sourcing and high-impact launch assets – all at a lower total cost.
Contact our expert team to discuss your project and discover how we can help you achieve your goals.
Request a ConsultationEvery project follows a structured and transparent methodology divided into four 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 ingredients addressing 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.
Global sourcing of products or manufacturers (focus on Europe) to identify selected finished products or suppliers matching your specifications.
Conduct a comparative assessment of shortlisted products and manufacturers across predefined criteria, and directly engage with selected factories to confirm territorial availability, regulatory compliance, and technical compatibility.
Develop a robust negotiation framework once a suitable manufacturer has been identified – defining the client's strategic preferences, constraints, target price ranges and partnership expectations.
Conduct the commercial negotiation on the predefined framework, leading detailed multi-round discussions with the manufacturer to align on core commercial, technical and regulatory terms.
Prepare structure, and review the contractual package covering all relevant operational, quality, regulatory, commercial, and technical provisions – to secure a robust final agreement.
Define final branding, packaging, artwork, and regulatory compliance text in multiple languages aligned with target market requirements.
Prepare and compile the registration dossier required in your country, ensuring regulatory compliance.
Develop scientific marketing content tailored to the product and target market, ready to support medical, regulatory, and commercial teams.
Develop and deliver product training programs for sales teams and medical representatives, integrating pathology insights, product science, clinical evidence, medical positioning, and go-to-market strategies to enhance field performance.
Oversee the full production and delivery cycle – coordinating manufacturing activities, quality milestones, logistics, customs documentation, and LC procedures to ensure on-time and compliant EXW delivery.
Obtain complementary scientific, clinical, or technical reports to strengthen product value or compliance.
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.
Access specialized legal expertise for contract review, compliance validation, and risk mitigation.
Manage ongoing supplier relationships, including performance tracking and issue resolution.
Full shipping management to final destination, including customs clearance and logistics.
Support full technology transfer processes between manufacturers and target territory.
Interested in one or more of these add-ons?
Contact Our Expert TeamYou aim to bring a high-quality European product to your market - but you lack the time, internal resources, or the full spectrum of scientific, industrial, regulatory and marketing capabilities to execute the launch efficiently.
Selecting the wrong product, an unreliable supplier, a poorly framed agreement, or preparing your launch without the right regulatory, industrial and scientific support can undermine the entire process.
Inconsistent execution at any stage compromises time, quality, cost control and commercial outcomes.
SCPS delivers a turnkey launch solution from Europe. We act as your dedicated European partner, managing all four strategic phases:
No travel, no operational distraction. You stay focused on your business while we deliver every step - from market analysis to launch coordination.
What may take your team 250 hours / 12 months - or a traditional consultant 200 hours / 9 months - SCPS delivers in 150 hours / 7 months.
You save time, effort and cost - and gain access to combined scientific, industrial, regulatory and strategic expertise you don't have in-house.
SCPS transforms fragmented complexity into structured, high-performance execution.
You retain full strategic control - while we secure time, quality, and return on investment.
The following example illustrates the value SCPS can deliver in a typical streamlined engagement:
A client aiming to introduce 10,000 units of a high-potential healthcare product in the GCC region delegates the full upstream launch process to SCPS. With an investment starting from €5,700, the client benefits within 5 to 6 months from:
Savings:
This scenario highlights SCPS's ability to deliver accelerated, low-risk, high-impact product launches, at a cost significantly lower than traditional consulting engagements.
Actual costs depend on the project scope, selected service modules, and desired level of customization.
Tell us about your product vision and market goals. Our team will prepare a customized project scope and timeline for your ready-to-market solution.
contact@scps-experts.com
+33 1 23 45 67 89
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