A 100% online, dynamic and intensive program through which you will get to know in detail the normative and regulatory framework of cosmetic production, as well as the novelties related to this field"

Safety, efficacy and the free market are the three fundamental pillars on which regulatory compliance in the manufacture and distribution of cosmetic products is based For this reason, Pharmacy professionals who dedicate their activity to this sector must know in detail the novelties related to the legislation and regulations that govern it, with the purpose of always working on the basis of the benefit of the person who finally ends up using it and avoiding possible legal problems for the company of which it is part.

This is why TECH has considered it necessary to launch this Postgraduate diploma in Regulation of Cosmetic Products, an avant-garde, intensive and dynamic program that includes the latest advances that have occurred, not only in the international legal framework, but also in relation to the development and manufacturing processes. In addition, it also delves into the current specifications of quality, efficacy and safety controls, as well as the strategies and procedures that have achieved the best results to date.

It will include 450 hours of diverse theoretical, practical and additional content presented in different formats and framed in a convenient and accessible 100% online program. In addition, in order to always guarantee the best educational experience, the graduate will be able to adapt the schedule to his/her own availability, as well as access the virtual classroom from any device with internet connection. Thanks to this, you will be able to update your knowledge with total guarantee and with the endorsement of a great scientific university such as TECH.

You will delve into new developments related to quality controls, efficacy and safety in the production of cosmetics through 450 hours of the best theoretical, practical and additional content"

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 self-assessment can be used to improve learning
• Its special 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

An educational experience at the forefront of the pharmaceutical sector, including case studies based on real-life situations, so you can hone your professional skills"

The program’s teaching staff includes professionals from the sector who contribute their work experience to this educational program, as well as renowned specialists from leading societies and prestigious 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 throughout the program. This will be done with the help of an innovative system of interactive videos made by renowned experts.

You will work on the latest developments related to cosmetic development and manufacturing strategies, so that you can apply them, from day one, to your professional practice"

As long as you have an internet connection, you will be able to access the Virtual Classroom whenever you want during the 6 weeks of this Postgraduate diploma"

The structure of this Postgraduate diploma has been designed by the teaching team, which has selected the most cutting-edge and innovative information in the sector, based on the demanding quality criteria that define and characterize TECH Thanks to this, it has been possible to compile 450 hours of theoretical, practical and additional content, including detailed videos, self-knowledge exercises, images, dynamic summaries, research articles and complementary readings. In this way, the graduate will be able not only to update his or her knowledge, but also to deepen the aspects he or she considers most important for his or her professional performance.

If you are looking to get up to date on the procedures to follow for the registration of products in the European portal, this program will give you the keys to achieve it quickly and effectively"

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. Regulatory Department: functions

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: 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. Cross-cutting 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 Cosmetics 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. Compacts: 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 and Compatibility
3.1.2. Preservative Efficacy
3.1.3. Controls in Process

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"