Research & Development
How to start a collaboration for the development of the SURACTIVES® forms for a food supplement
Innovative food supplements ingredients
Full service High-quality forms of innovative food supplements for oral use.
Specialized development and Support
We provide specialized technical Development and manufacturing support.
Compliance with Regulations
Evaluation of quality parameters and compliance with domestic and international regulations.
3d party contract manufacturer
We offer collaboration for third parties and for the development of new projects.
Innovative food supplements ingredients
Full service High-quality forms of innovative food supplements for oral use.
Specialized development and Support
We provide specialized technical Development and manufacturing support.
Compliance with Regulations
Evaluation of quality parameters and compliance with domestic and international regulations.
3d party contract manufacturer
We offer collaboration for third parties and for the development of new projects.
New products develompent
The IPS – SURACTIVES® Division excels as a third-party contract manufacturer, specializing in R&D and the industrial-scale production of cutting-edge food supplements featuring controlled release and taste masking. Our collaborative process is meticulously structured, with each phase commencing only after the successful completion of the preceding one, ensuring precision and quality at every step.
Active Ingredient Profiling
Comprehensive profiling of the active ingredients physicochemical properties, including solubility, particle size, and analytical methods, backed by relevant certificates of analysis. This step ensures a thorough understanding of each ingredient, encompassing supply sources and essential quality parameters.
Collaborative Product Design
Collaborative exploration with the partner company to define the finished product’s specifications, including:
- Selection of the final form (e.g., capsules, tablets, single-dose bottles, or sachets) for development
- Determination of the active ingredient dosage per unit,
- Analysis of the in vitro release duration of active ingredients, considering their half-life and potential need for repeated doses
- Establishment of trial and pilot batch sizes
Tests of coating
Tests of coating of the active ingredients
Production of Trial batch
Production of a trial batch having the desired in vitro controlled release pattern.
Production of Pilot Batch
Production of a pilot batch corresponding to the characteristics described at point 2, accompanied by all the relevant technical specifications, including:
- Method for the determination of the in-vitro release pattern
- Quali-quantitative composition
- Production method
Our Technologies & Brands
PATENTED COATING TECHNOLOGIES
Discover our coating technologies and registered trademarks.