Hot Melt Extrusion
Product Description
Sever Pharma Solutions
-
Country/Region:Sweden
-
On CPHI since:2023
-
Certificates:2
-
Employees:250 - 499
Company types
Primary activities
Categories
Specifications
Sever Pharma Solutions
-
Country/Region:Sweden
-
On CPHI since:2023
-
Certificates:2
-
Employees:250 - 499
Company types
Primary activities
More Products from Sever Pharma Solutions (3)
-
Product Aseptic fill and finish PFS 1mL Long Format and Autoinjector Assembly
We offer solutions for companies that need CMO capacity concerning the aseptic filling of syringes and assembly and packaging of pre-filled syringes and auto-injectors. We will enhance your product by adding value through manufacturing if you require additional capacity or a complete technology transfer. q... -
Product High-potent Dosage Forms up to OEB6
We have the experience, expertise, and facilities at Sever Pharma Solutions to safely work with your high-potent substances. This includes manufacturing products containing APIs that are ranked in the highest occupational exposure bands (OEB) up to and including OEB6.
Our focus on safety starts ... -
Product Polymer-based delivery systems
Polymer-based dosage forms continuously administer the drug to the patient for an extended period, varying from weeks to years. These controlled-release products are very suitable for specific indications, patient populations, and drugs due to the long duration of action, avoidance of first-pass metabolism...
Sever Pharma Solutions resources (7)
-
News Sever Pharma Solutions expands partnership with Silo Pharma
Sever Pharma Solutions, a leading Contract Development and Manufacturing Organization (CDMO) specializing in controlled release systems for high potent drugs, today announced an expanded agreement with Silo Pharma, Inc. (Nasdaq: SILO), a biopharmaceutical company developing novel formulations and drug delivery systems for traditional therapeutics and psychedelic treatments. Under the new agreement, Sever Pharma Solutions will scale up extrusion processes and continue analytical testing for Silo’s investigational SP-26 ketamine-loaded polymer implant targeting chronic pain and fibromyalgia. -
Brochure Who we are - introduction to Sever Pharma Solutions
Sever Pharma Solutions offers a comprehensive range of CDMO Services allowing us to support drug product development from start to finish. Our expertise includes Polymer-BasedDelivery Systems, Highly Potent Compounds (up to OEB6), Hormonal and Controlled DEA Substances (Schedule 3-5). -
Video Inside Our Putnam Site: Purpose-Built for Your High Potent Projects
Sever Pharma Solutions US site in Putnam, CT, features two fully commissioned and qualified High Potent API handling suites: One for development, one for GMP manufacturing. Designed with twin and single screw extrusion in mind, these suites bring flexibility, safety, and efficiency to your drug product development journey. From early-stage proof-of-concept in our ISO 8 development suite to seamless scale-up in our ISO 7 GMP suite, Putnam is engineered to eliminate unnecessary tech transfers and reduce timelines — without compromising quality or safety. See what makes Putnam a uniquely capable partner for your most challenging formulations. -
Video Inside Our Malmö Site: Dedicated to GMP and non-GMP development
Sever Pharma Solutions’ facility in Malmö, Sweden, features state-of-the-art suites dedicated to GMP and non-GMP development of polymer based delivery systems. Our Malmö site utilizes advanced polymer extrusion technologies for the production of implants, drug eluting intrauterine devices and intra-vaginal rings. The air circulation in the suites is single pass and state-of-the-art engineering controls are in-place for ensuring adequate containment for operator safety and prevention of cross-contamination. The recent addition of a three-layer co-extruder further enhances our offering, enabling the production of multilayered fibers with customized drug release profiles. Malmö is now uniquely positioned to streamline your drug development journey, delivering flexibility, safety, and efficiency. -
Whitepaper Design of intra-vaginal drug-releasing rings
Download our free whitepaper on the design of intra-vaginal drug-releasing rings (IVRs) and the importance of avoiding unnecessary design complexity. You will also get the background on IVR development, which includes polymer selection and drug release kinetics, and learn more about simultaneous drug release. -
Whitepaper A COMPARISON OF SATURATED SOLUBILITY ENHANCEMENT VIA SPRAY DRYING AND HOT MELT EXTRUSION PROCESSING
Solid solutions are similar to liquid solutions and consist of a single phase irrespective of the number of components. A solid solution of a poorly water-soluble drug dissolved in a carrier is particularly interesting in improving oral bioavailability. In a solid solution, the drug’s particle size has been reduced to its molecular dimensions resulting in a more rapid dissolution rate. By judicious selection of a carrier, the dissolution rate of the drug can be increased by up to several orders of magnitude. In a solid solution, the drug’s particle size has been reduced to its molecular dimensions resulting in a more rapid dissolution rate.
This whitepaper compares solubility enhancement between spray drying and hot melt extrusion for a poorly soluble, new active pharmaceutical ingredient.
-
Whitepaper ANALYTICAL TOOLS & TECHNIQUES IN HOT MELT EXTRUSION - CASE STUDY ON PROCESS SCALE UP
Hot melt extrusion has been widely used as a processing method for many purposes, including forming a solid molecular dispersion to increase the bioavailability of poorly soluble drugs. Analytical tools and techniques can significantly reduce time and improve success rates in developing hot melt extrusion formulations.
In the scale-up phase, analytical characterization techniques ensure similar solubility enhancement occurs on larger extrusion equipment as with the lab scale equipment used for formulation development.
In this whitepaper, you will learn more about the analytical characterization and techniques that are critical in the scale-up of melt-extruded solid dispersions to ensure similar products are produced, specifically in obtaining similar solubility-enhancing effects.