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CosmetoSAFE Assist – we have a solution for technologists’ needs!

Creating a cosmetic product is, on the one hand, an ambitious conceptual task – we must demonstrate creative inventiveness in terms of the declared properties of the product, its composition and application properties. On the other hand, the legislator imposes on us the obligation to ensure appropriate repeatability of production, stability, microbiological purity and safe use of the product. And finally, evidence of the claimed effect of the cosmetic. The work of a technologist requires technical skills and time to perform all necessary activities in the laboratory. In addition, the technologist must collect, process and properly archive a lot of information: raw material dossier, test results, packaging data, etc. 

Having worked with cosmetic technologists for a decade years now, developing cosmetic safety assessment reports, we largely work on the same data (documents), we can see what problems they face on a daily basis. Based on this experience, we have created CosmetoSAFE Assist – this is an intuitive tool designed to facilitate the daily work of cosmetic companies’ R&D teams, Iwona Białas concludes. 

What is CosmetoSAFE Assist? 

CosmetoSAFE Assist is CosmetoSAFE Consulting’s proprietary tool supporting the work of technologists, product documentation specialists, regulatory departments or product managers, which comprehensively addresses product assumptions. Its aim is to increase productivity and effectiveness of work as well as minimising the risk of errors.  The tool cuts the time spent working on cosmetic product documentation by: 

  • automation of product documentation (PIF), concentration calculations or price calculations, 
  • efficient management of formulations, raw material documentation and related information, 
  • assessing compliance with the requirements for marketing statements, 
  • enabling the tracking of blacklists and information on banned substances. 

In our view, automation is also an opportunity for organisations to effectively manage their internal know-how. When presenting CosmetoSAFE Assist, we cannot promise that all the red-tape activities related to cosmetics creation can be transferred to data processing tools: in our solution, techno­logists still have to analyse the raw material dossier, properly assess the quality and suitability of raw mate­rials or packaging to his or her requirements, but note that they perform these activities for a given item on a one-off basis (according to our proprietary data archiving system) and then use the conclusions in future implementations – until, obviously, the next change of a given item takes place, sums up Iwona Białas. 

 

How do companies work with product and raw material documentation today? 

The development of a cosmetic product is, on the one hand, a challenging conceptual task – we have to be inventive in terms of the claimed properties of the product, its composition, and its application properties. On the other hand, the legislator imposes on us the obligation to ensure adequate repeatability of manufacturing, stability, microbiological purity or safety of product application and, finally, evidence of the claimed cosmetic effect. The technologist’s job requires technical skills and time to perform all the necessary activities on the laboratory side. In addition, the technologist must collect, process and properly archive a lot of information: raw material dossier, test results, packaging data, etc. 

The results of the survey confirm that, in the era of almost geometrically increasing legislative changes, working on product documentation takes more and more time. The matter becomes even more complicated when legislative changes require rapid implementation into product items present on the market. When asked how much time it takes them to work on product reformulations and adaptations of formulations to legislative changes, technologists indicated a decidedly greater involvement in this type of activity in relation to 2020: for 10% of respondents, product updates today take up approx. 50% of their working time (less than 4% of respondents gave such an answer in 2020); for 25% of the respondents, it is between 30 and 50% of their time (almost twice as many respondents chose this answer when compared to 2020). 

Technologists note the lack of human resources to deal mainly with documentation. In particular, the constant recipe changes generate a huge amount of work related to updating the PIF or safety assessment of the finished product. An additional problem is that the documents provided by suppliers are not prepared according to a uniform template. Sometimes they are incomplete or even incorrect, or are difficult to obtain. Significantly, the lack of human resources to complete the documentation is a problem indicated by 58% of respondents today, while three years ago it was 33% of respondents. 

When asked about the tools and/or system solutions used for recipe creation and related duties (concentration calculations, labelling, etc.), as many as 72% of survey participants said that they only use Microsoft Excel. For mass production costing tools, 84% of respondents admitted that they use Excel for this purpose, too. Those who use other software for documentation work most often use ERP or other in-house systems. 

Interestingly, there is a growing awareness among R&D employees of the possible use of automated solutions in their work. In 2020, only 6.17% of respondents complained about the lack of appropriate tools that would systemically help manage data, compared to nearly 30% today. 

If You plan new sun care products launching, it is good to know the current legislative status!
𝗛𝗮𝘃𝗲 𝘆𝗼𝘂 𝗲𝘃𝗲𝗿 𝘄𝗼𝗻𝗱𝗲𝗿𝗲𝗱 𝗵𝗼𝘄 𝗺𝗮𝗻𝘆 𝗰𝗼𝘀𝗺𝗲𝘁𝗶𝗰 𝗶𝗻𝗴𝗿𝗲𝗱𝗶𝗲𝗻𝘁 𝗿𝗲𝗴𝘂𝗹𝗮𝘁𝗶𝗼𝗻𝘀 𝘄𝗲 𝗵𝗮𝘃𝗲 𝘁𝗼 𝗶𝗺𝗽𝗹𝗲𝗺𝗲𝗻𝘁 𝗶𝗻 𝗼𝘂𝗿 𝗼𝗿𝗴𝗮𝗻𝗶𝘇𝗮𝘁𝗶𝗼𝗻𝘀 𝗽𝗲𝗿 𝘆𝗲𝗮𝗿?
Creating a cosmetic product is, on the one hand, an ambitious conceptual task – we must demonstrate creative inventiveness in terms of the declared properties of the product, its composition and application properties. On the other hand, the legislator imposes on us the obligation to ensure appropriate repeatability of production, stability, microbiological purity and safe use of the product.