Develop and implement internal standard operating procedures (SOP's, Quality Systems, Good Manufacturing Practices,...).
Review of installations (own and/or subcontracted) to verify compliance with current regulations.
Conducting quality audits.
Assist in the implementation of quality systems and GMP/GMP.
Manage authorizations/licenses for product manufacturing and/or importing companies.
Preparation of the Responsible Declaration of cosmetics facilities, for companies located in national territory, which carry out any of the manufacturing or import activities and submission to the Spanish Agency of Medicines and Medical Devices.
Search for subcontractors.
Pre-evaluate products by advising on ingredients, claims, etc.
Editing and revision of global labeling, to cover most of the countries where the product is to be marketed.
Manage the information dossier, Product Safety Report and notifications or records of the products, according to their category.
Registration management for the export of products (Certificate of Free Sale FSC/CLV, Apostilles,...).
Cosmetics CPNP Notification.
Information dossier for registration and export of products to other countries. Labeling. Request for National Code for distribution to Pharmaceutical Distributors and Pharmacy Offices (Voluntary).
Legally responsible before the EU health authorities.
Responsible for ensuring that products arriving in the EU comply with European regulations.
Responsible for Cosmetovigilance and advertising / promotional actions of products.
Product import support (reception, customs management, storage and picking).
Manage safety and efficacy trials (clinical or in vitro).
Cosmetovigilance/market surveillance management.
Processing of advertising in medical devices or in Autocontrol.
Advice on safety and efficacy studies.
Design of protocols for efficacy studies.
Advice on consumer messages based on the studies carried out.
Technical review of content for Social Networks.
Training sessions.
Regulatory alerts.
We unlock projects and provide your company with access to the entire value chain to find solutions.
1. We carry out a diagnosis and become aware of the reality of the project, its timelines and milestones.
2. We offer our services in full service mode or in collaboration with the technical areas of your company.
Formulation and R&D
Formulation review.
Product development.
Repositioning of lines.
Applications laboratory available to customer formulators.
Quality
Develop and implement internal standard operating procedures (SOP's, Quality Systems, Good Manufacturing Practices,...).
Review of installations (own and/or subcontracted) to verify compliance with current regulations.
Conducting quality audits.
Assist in the implementation of quality systems and GMP/GMP.
Manage authorizations/licenses for product manufacturing and/or importing companies.
Preparation of the Responsible Declaration of cosmetics facilities, for companies located in national territory, which carry out any of the manufacturing or import activities and submission to the Spanish Agency of Medicines and Medical Devices.
Search for subcontractors.
Regulatory
Pre-evaluate products by advising on ingredients, claims, etc.
Editing and revision of global labeling, to cover most of the countries where the product is to be marketed.
Manage the information dossier, Product Safety Report and notifications or records of the products, according to their category.
Registration management for the export of products (Certificate of Free Sale FSC/CLV, Apostilles,...).
Cosmetics CPNP Notification.
Information dossier for registration and export of products to other countries. Labeling. Request for National Code for distribution to Pharmaceutical Distributors and Pharmacy Offices (Voluntary).
Responsible person
Legally responsible before the EU health authorities.
Responsible for ensuring that products arriving in the EU comply with European regulations.
Responsible for Cosmetovigilance and advertising / promotional actions of products.
Product import support (reception, customs management, storage and picking).
Toxicology, Clinical, Medical Marketing
Manage safety and efficacy trials (clinical or in vitro).
Cosmetovigilance/market surveillance management.
Processing of advertising in medical devices or in Autocontrol.
Advice on safety and efficacy studies.
Design of protocols for efficacy studies.
Advice on consumer messages based on the studies carried out.
Training
Training sessions.
Regulatory alerts.
3. We unlock projects and provide your company with access to the entire value chain to find solutions.
Any company, whatever its size, maturity or level of expertise, needs support to undertake a new and disruptive project.
We offer you a comprehensive and modular service
MuttuLab offers a comprehensive and modular service to help companies unlock their cosmetic projects and bring them to fruition.
Diagnosis of your project
From MuttuLab we make a deep diagnosis of the project, its current status, possible threats or blocking places.
After the diagnosis, we establish an individualized work plan with your company, collaborating with the technical areas and/or carrying out the necessary activities for the progress of the project.
The MuttuLabers recommend us to
"They have helped me to train myself and to move my project forward."
"I have been working with them since I started. They have helped me to train myself and to move my project forward. I am very happy to be part of MuttuLab, and I hope to be for many years!".
Dolça Pallàs SAB.solids
"100% Recommended."
"Muttulab helped us from the start of the company in 2018 and to this day with the launch of all our products. They are very resolute and helpful. Their long track record is a fundamental piece, which has helped us solve all the problems we have encountered along the way. Without a doubt, they are a key partner in the company and their charisma and pragmatism are skills that make the difference."
Jordi Ripollès CEO & Co-Founder at VALY COSMETICS
"The best thing about MuttuLab is the 360 service."
"They helped us both initially with some formulations and with the subsequent legalization of the products and the design of the dossiers. They combine product and regulatory knowledge, a global service that is hard to find."
Eric Steinbauer Co-CEO of KRIIM
"They have helped me to train myself and to move my project forward."
Dolça Pallàs SAB.solids
"100% Recommended."
Jordi Ripollès CEO & Co-Founder at VALY COSMETICS
"The best thing about MuttuLab is the 360 service."
