CordenPharma Lipid Data Sheet > C12-200

CordenPharma’s vertically-integrated supply chain model provides development & manufacturing expertise spanning the complete GMP supply chain. Beginning with regulated Key Raw Materials and Non-GMP Intermediates, our sister organization WeylChem supports back integration to sec...

Sterile Drug Product manufacturing requires dedicated and specialized capabilities which are in compliance with FDA aseptic guidance and EMA regulatory requirements. CordenPharma has a long track record of experience in manufacturing Parenteral Sterile Solutions and Emulsions in different pharmaceutical fo...

CordenPharma’s service offerings include a wide range of products, formulations and services supporting new chemical entities, re-formulations and generics:
• Powder & Granule-filled Capsules • Powder Granules & Pellets • Immediate Release Tablets • Controlled Release Tablets • Mini-tablets...

LipidsCordenPharma’s scientists have mastered the chemical total synthesis of complex derivatized phospholipids from multi-gram to multi-kilogram scale and are renowned for their contract lipid and phospholipid manufacturing expertise. Our large-scale proprietary cGMP manufacturing processes star...

CordenPharma’s expert lipid manufacturers have mastered the chemical total synthesis of complex phospholipid derivatives from multi-gram to multi-kilogram scale and are renowned for their contract lipid and phospholipid molecule manufacturing expertise. Our large-scale proprietary cGMP manufacturing proces...

CordenPharma also pioneered the chemistry and large-scale manufacture of MPEG-conjugated phospholipids which can be accessed through a synthesis cascade, rendering them superior quality phospholipid examples for sensitive liposome formulation processes.
• MPEG-2000-DMPE - CAS No 384835-59-0 ...

• PACKAGING DEVELOPMENT - CordenPharma manages all the logistical procedures involved in packaging development by creating and producing your packaging components. From layout development and producing a printable copy to procuring the materials, we work with creativity and precision. • PACKAGING -&...

CordenPharma has extensive experience in sterile contract manufacturing with a wealth of lyophilization expertise. In particular, the optimization of the freeze drying process as it relates to cycle times represents a critical attribute for complex parenteral product development. CordenPharma experts suppo...

CordenPharma is uniquely positioned to support Veterinary Health companies in the Contract Development and Manufacturing of their Oral Drug Product requirements - with particular expertise and a dedicated, segregated building exclusively for the manufacture of Veterinary Drug Products which have not been p...

CordenPharma combines considerable R&D development resources with a wide range of manufacturing capacity to assist with your project at any stage of clinical development and projected commercial scale of supply.

Our extensive reactor capacity of over 1,200,000 L total volumetric capacity spr...

At any development stage and scale of synthesis CordenPharma’s services for contracted customers include all supporting activities that are required to be adequately cGMP compliant such as:
• Process Validation • Cleaning Validation • Batch Release • Analytical Method Development & Validation •...

SUPPORT SERVICES FOR OUR CONTRACTED CUSTOMERS • Analytical Development • Validation Support • Regulatory Support • Clinical Supply Services

CordenPharma, the CDMO specialising in APIs, lipid excipients, and drug products, signs a new billion dollar contract to expand its manufacturing capabilities. 

Register for this Live (4-4-18) or on Demand webinar to learn how the most important (and often over-looked) aspect to a robust containment program is the strength of the intangible, softer elements. Discuss how to maximize the success of your engineering control investments and allow for continued alignment to your company’s commitment to providing a workplace free of recognized health & safety hazards.