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Product development
Research & Development
All new products are developed and tested in our in-house laboratory. Medical or cosmetic products, natural or conventional, with us you are getting everything from one provider.
A particular area of strength in this regard is the attention paid to customer-specific wishes and current market trends.
Technical Marketing
This is where we focus on your target market and your target group in order to implement your product preferences accurately and in a marketing-oriented manner.
The services we offer include:
- the creation of individual product concepts,
- identifying trends and market tendencies in the targeted sector
- desired product positioning in your existing product range
- claims and claim substantiation Recommendations
- technical customer advice on raw and active substances, taking the desired restrictions into account
- product development consulting in accordance with the COSMOS natural cosmetics standard
Quality Assurance
Numerous tests and quality controls secure the production processes and guarantee flawless and consistently high quality.
Our partner laboratories:
- Stability testing
- Microbiology
- Processing test
- Dermatological tests
- GMP- Good manufacturing practice
- Documentation
Regulatory Affairs
A safe product also has to include the appropriate declaration, documentation and registration. You receive all of these services directly from us – professionally, fairly and without bureaucracy.
Cosmetics placed on the EU market must be announced or “notified” before being placed on the market. This is stipulated by Article 13 of EU Regulation No 1223/2009 on cosmetic products. We support you in registering your company and providing notification of your cosmetic product with the Cosmetic Products Notification Portal (CPNP).
We create the required product information file (PIF) pursuant to Art. 11 of the EU Regulation on cosmetic products. This PIF contains, among other things, the description of the cosmetic product, the production methods, as well as the safety report including the safety assessment. You may act as the responsible person pursuant to Article 4 of the EU Regulation on cosmetic products.
You will receive all the necessary information for creating your print data. This includes not only the mandatory details such as “ingredients” and the intended use; we also check the optional details and claims of your cosmetic product, in consideration of the statutory requirements. This is where we offer you some initial assistance.
As a producer of cosmetic products and medical devices, we are certified in accordance with EN ISO 9001 and EN ISO 13485. A key principle of EN ISO 9001 is process orientation. The international standard EN ISO 13485 is the standard for quality management systems in the area of medical devices. In addition to the positive quality effects, certification is often also a prerequisite for exporting our products.
