With this program, the professional will delve into the medical, hygienic and quality Regulation of Cosmetic Products, allowing them to know the latest evaluative standards" 

The production and mass production of cosmetics must be regulated and supervised to meet the standards required by the field of action. This process depends to a great extent on an exhaustive analysis and quality control that serves to prevent adverse effects in medicated patients. In this way, the regulatory process becomes one of the most important and demanding to endorse a product.

This is why the presence of medical professionals is necessary in the rigorous process for the distribution of a product, who from their knowledge and experience seek excellence in each product, and that this in turn works under high quality standards. To this extent, the Postgraduate diploma in Regulation of Cosmetic Products seeks, from its content, teaching staff and study material, to update the knowledge and study material, to update the knowledge of medical professionals so that they can identify, analyze and decide which cosmetics are and are not useful to treat skin conditions and diseases. 

For this reason, TECH is launching this program in order to guide the physician through the informative path of updating and regulating cosmetic products. In addition, the program is an avant-garde, intensive and highly demanding educational program. The specialist will be able to delve into the regulatory processes that will allow themr to identify viable and non-viable products for the different types of different types of treatment.

This innovative program designed by TECH has a first class theoretical and practical content, specifically selected to bring out the highest potential of its graduates. To do this, the student can access the virtual campus whenever they want, meaning you can also download all the content of the program to study it whenever you want to.

With this program, you will be able to update your knowledge in the relevant regulations of the elaboration of cosmetic products" 

This Postgraduate diploma in Regulation of Cosmetic Products contains the most complete and up-to-date scientific program on the market. The most important features include:

• Practical cases presented by experts in Cosmetic Science and Technology
• The graphic, schematic, and practical contents with which they are created, provide scientific and practical information on the disciplines that are essential for professional practice
• Practical exercises where the self-assessment process can be carried out to improve learning
• Emphasis on innovative methodologies
• Theoretical lessons, questions to the expert, debate forums on controversial topics, and individual reflection assignments
• Content that is accessible from any fixed or portable device with an Internet connection

Access the content of the Virtual Campus to get up to date with the latest updates in the dermatological sector to identify the due process of cosmetic products and their regulation for medical use"

The program includes, in its teaching staff, professionals from the sector who bring to this program the experience of their work, in addition to recognized specialists from prestigious reference societies and universities.

The multimedia content, developed with the latest educational technology, will provide the professional with situated and contextual learning, i.e., a simulated environment that will provide immersive education programmed to learn in real situations. 

This program is designed around Problem-Based Learning, whereby the professional must try to solve the different professional practice situations that arise during the academic year For this purpose, the student will be assisted by an innovative interactive video system created by renowned and experienced experts. 

Find out what the current requirements are for the endorsement of cosmetics, identifying from your role as a doctor if they are viable for use of dermatological problems"

Identifies the best cosmetic products that can help the patient's dermatological treatment based on their quality"

The syllabus of this Postgraduate diploma in Regulation of Cosmetic Products has been designed by an experienced faculty that from its interpretative capacity has been able to discern about the most effective cosmetic products in the field. With a duration of 450 hours, the program promises to guide the medical professional on their way to update their knowledge in the on their way to updating their knowledge in the regulation of products and their quality at the time of medical treatment.

Update your knowledge on cosmetic product regulation to know the feasibility and effectiveness of cosmetic products" 

Module 1. International Legislation on Cosmetic Products

1.1. Regulations in Europe

1.1.1. European Regulations-Legislation
1.1.2. Regulation 1223/2009
1.1.3. Borderline Products

1.2. Requirements for Importers, Distributors and Providers Placing the Product on the Market

1.2.1. Definitions Based on European Legislation
1.2.2. Obligation Based on European Legislation
1.2.3. Product Notification Portal Registration

1.3. Cosmetic Laboratory Areas

1.3.1. Department Definitions
1.3.2. Materials and Personnel Flow
1.3.3. Industrial Equipment and Instrumentation

1.4. Regulation Department: Function

1.4.1. Safety Assessor
1.4.2. Safety Assessment and Product Dossier
1.4.3. Safety Assessment: Studies

1.5. ISO Standards and Certifications

1.5.1. Good Manufacturing Practices
1.5.2. Natural Cosmetic Products
1.5.3. Quality

1.6. Regulations: The USA, Latin America and Asia

1.6.1. U.S. Legislation
1.6.2. Latin American Legislation
1.6.3. Legislation in Asia
1.6.4. Export Requirements

1.7. Transversal Legislation

1.7.1. REACH Legislation
1.7.2. CLP Legislation
1.7.3. Other Legislation: Toys, Biocides, Others

1.8. Other legislation

1.8.1. European Legislation: Borderline Products
1.8.2. Personal Care Products
1.8.3. Aerosol Legislation

1.9. Registration Requirements for Cosmetic Products in Other Countries (FDA, USA)

1.9.1. Customs Services
1.9.2. Labeling Requirements
1.9.3. Differences in Definition between Cosmetics and Medication

Module 2. Cosmetics Development and Manufacturing

2.1. The Cosmetic Industry

2.1.1. The Cosmetic Industry Sector
2.1.2. Briefing or Initial Idea
2.1.3. Laboratory to Pilot Testing

2.2. Cosmetic Product Manufacturing Processes

2.2.1. Manufacturing and Subsequent Quality Control
2.2.2. Packaging, Conditioning and Labeling
2.2.3. Storage and Distribution

2.3. Raw Materials for Cosmetics Manufacturing

2.3.1. Water Used in the Cosmetic Industry
2.3.2. Antioxidants and Preservatives
2.3.3. Moisturizers, Emulsifiers, Silicones and Polymers

2.4. Cosmetic Packaging

2.4.1. Materials
2.4.2. Trends in Cosmetic Packaging
2.4.3. Packaging for Children's Cosmetics

2.5. Manufacturing Operations and Processes in Different Cosmetic Forms

2.5.1. Good Manufacturing Practices for Cosmetic Products UNE-EN-ISO: 22716:2008
2.5.2. Formulations Prior to Cosmetic Development
2.5.3. Prototypes Preparation and Formulation Examples

2.6. R&D in Cosmetic Product Development

2.6.1. New Cosmetic Forms
2.6.2. TOP Cosmetic Ingredients
2.6.3. New Plant-Derived Ingredients

2.7. Solution, Suspension and Emulsion Preparation

2.7.1. Textures
2.7.2. Aqueous, Micellar and Oily Solutions
2.7.3. Suspensions and Emulsions
2.7.4. Gels and Cremigels

2.8. Solid and Semi-Solid Cosmetics Preparation

2.8.1. Sustainability and Practicality
2.8.2. Sensoriality and Efficiency: New Formats

2.8.2.1. Soaps and Syndets
2.8.2.2. Ointments and Salves

2.8.3. Loose Powder vs. Compact: Uses

2.9. Other Cosmetic Forms and Substrates

2.9.1. Aerosols
2.9.2. Foams
2.9.3. Single Doses

2.9.3.1. Mask Tissue
2.9.3.2. Impregnated Wipes

2.10. Perfume Manufacturing

2.10.1. Perfume: Background
2.10.2. Raw Material Origin, Composition and Application
2.10.3. Alcoholic Fine Perfumery
2.10.4. IFRA Standards

Module 3. Quality Control, Efficacy and Safety in Cosmetics

3.1. Quality Controls

3.1.1. Stability- Compatibility
3.1.2. Preservative efficacy
3.1.3. Process Control

3.2. Article 19 Cosmetics Regulation Based on Study Results

3.2.1. ISO Definitions for Products Susceptible of Microbiological Risk
3.2.2. Shelf Life and ODP Calculation
3.2.3. Labeling Analysis

3.3. Good Manufacturing Practices

3.3.1. Standard Operating Procedures: Manufacturing and Packaging
3.3.2. Third Party Contracts
3.3.3. Hygiene and Personnel Training

3.4. Traceability

3.4.1. Standard Operating Procedures: Off-Spec Products
3.4.2. Cosmetovigilance
3.4.3. Product Recalls

3.5. European Portal Registration Procedures

3.5.1. Registering the Person in Charge
3.5.2. Cosmetic Product Registration
3.5.3. Framework Formula

3.6. Cosmetic Product Safety Report

3.6.1. Regulation 1223/2009: Annex I
3.6.2. Product Dossier
3.6.3. Safety Assessment: Toxicological Profile

3.7. Skin Compatibility Studies

3.7.1. Skin, Ocular and Mucosal Compatibility Studies
3.7.2. Labeling Claims
3.7.3. SPF Studies

3.8. Cosmetic Efficacy Studies

3.8.1. Studies on Efficacy
3.8.2. In vitro-In vivo
3.8.3. Ex Vivo – In Silico

3.9. Sensory Analysis

3.9.1. Sensory Analysis Studies
3.9.2. Instrumental Tests
3.9.3. Questionnaires and Assessment Criteria

3.10. Claims Regulation

3.10.1. Regulation 655/2013: Common Criteria
3.10.2. Guidelines to Substantiate Claims
3.10.3. "Free" Labeling Claims

An unparalleled opportunity to implement in your practice the most innovative and cutting-edge strategies related to R&D and development of cosmetic products. of cosmetic products"