Welcome to our training course on cosmetic regulations and DIP drafting! This three-day (21-hour) course will enable you to master regulatory requirements (R1223/2009, GMP, IFRA)., to understand current practices in industry and craftsmanship, and to compile and draft a Product Information File (PIF) before submitting it to the cosmetic product evaluator.
We support you so that you can develop your business in the best possible way!
General information
Definition of a cosmetic product
Regulatory context:
- European Cosmetics Regulation 1223/2009
- The supervisory authorities (ANSM, DGCCRF, customs)
- IFRA
- The SCCS
- The European Cosmetic Products Notification Portal (CPNP)
The product information file (PIF)
General information – Content and structure of the file
Help with writing Part 1
Writing Part 2A:
- CosIng and verification of compliance with the annexes to the European regulation
- Qualitative and quantitative formula: INCI, CAS, mass percentage
- Physical and chemical characteristics and stability of the finished product
- DTP and DDM
- Microbiological quality: challenge test (CT) or justification for the absence of CT
- General information about packaging material: food/cosmetic/pharmaceutical compliance certification and packaging stability study
- IFRA compliance verification and allergen calculation
- Mandatory labeling information
- Calculation of traces and impurities
- Exposure to cosmetic products (according to the SCCS)
Good Manufacturing Practices (Part 3)
Claims and testing (Part 4)
Justification for the absence of animal testing (Part 5)
Obligations
Declaration to the ANSM
Batch records to be provided (stability study, label, packaging, test results, formulation, manufacturing sheet)
Regulatory monitoring: Updates and life of the DIP
Cosmetovigilance (reporting of adverse reactions and serious adverse reactions)
Notification of products on the CPNP
Case studies
Study of a DIP with parts 1, 2A, 3, 4, and 5
In particular, you will study:
- Determination of an INCI
- Determining the compliance of raw materials with European regulations
- Determination of a PAO/DDM
- Verification of compliance with IFRA
- Calculation of allergens
- Calculation of impurities
- Label verification
- Determination of exposure to the cosmetic product
- Notification on the CPNP portal
Time for discussion
During this time, our toxicologist will answer any personal questions you may have. Of course, we will also take the time to answer all your questions throughout the training course.
General information
Find the program for this training course in PDF format Download here.
Number of places: Maximum 12 participants per session
Audience: Anyone responsible for regulatory affairs or product development: business owners, artisans, project managers in the cosmetics industry.
Duration: 3 days (21 hours)
Price: €1,250 excluding tax
Materials to bring: PPaper, pencil, calculator, laptop.
Next session, contact us.
We are available to answer any questions you may have about this training course. Please feel free to contact us. contact us.
Laboratoires Lelégard SASU is a training organization registered under number 84030393603. This registration does not constitute state approval.