Many operations of the sales and operations planning in the pharmaceutical industry already exist but are managed independently by different pilots and often without coordination. The systemic approach remains unused because the organization has to be mature. From the outside
Subcontracting agreement : key points before signed
Today, thanks to internet, anyone can easily find standard contracts. However, we must remain vigilant on these contracts quality, because it is regularly found in the legal field that companies having used this type of template are highly contractually committed
ENT treatment: what is the point of integrating plants into health products?
Since the dawn of time, human beings use plants for their health benefits, for their culinary interest or for less shameful pleasures. Yes, who has never had the opportunity to enjoy a small glass of herbal liqueur!!! Plants have many
Quality defect :5 major points to respect in order to define a quality defect in a specification.
Between a pharmaceutical contract-manufacturer (CDMO) and the client, the specifications drafting phase corresponds in some ways to the phase in which the foundations of the project are laid. The phases following the specifications are intended to build the project from
ISO 13485 standard: what are the advantages and disadvantages of upgrading to 2016?
In our field, quality is very important. This is why the internationally recognized ISO 13485 standard establishes the requirements for a quality management system specific to the medical device field. In 2016, this standard was reviewed to allow convergence towards
ECOSOLUTION ™ the cosmetic packaging that protects your formulas and respects nature
Today, ensuring a customer experience that leaves up to the image of the brand is at the center of attention. Adding effectiveness of the formula, ease of use, attractiveness and pleasure while having an environmentally friendly approach is not always