Douglas CDMO offers comprehensive contract manufacturing solutions tailored to the needs of pharmaceutical and biotechnology companies, from development through to commercial scale production.
Leveraging our expertise in complex chemical structures, soft gel formulations, and cutting-edge manufacturing technologies, we ensure the highest quality standards for your products, in adherence to cGMP.
Scale up: From small-scale production to product launch
Douglas CDMO provides comprehensive support throughout the scale-up and process validation process. Our technical team ensures a seamless transition from laboratory to commercial manufacturing, whether scaling up within our facilities or undergoing a technology transfer.
Dosage forms
Douglas CDMO supports the manufacture of various dosage forms, including:
Solids
Our capabilities include solid oral dose and hard gelatine capsules, with or without containment requirements. We offer a range of processes such as high shear granulation, low shear granulation, drying, blending, Hardgel encapsulation, suppository encapsulation, compression, and coating.
Semi-solids
We can support all your semi-solid project needs and have experience in overcoming challenging API formulations. We produce a range of both topical and transdermal semi-solid dosage forms, including creams, gels and ointments.
Liquids
Douglas CDMO has extensive experience in liquid drug development and manufacturing. We develop a wide range of liquids, including solutions, emulsions and suspensions.
Softgel capsules
We have extensive capabilities and expertise in manufacturing softgel capsules. This includes formulating the inner fill medicine and encapsulating this within the softgel capsules.
Learn moreTechnology transfer
At Douglas CDMO, we offer cutting-edge solutions and ample capacity to support your requirements from initial development stages to full-scale commercial manufacturing. Our primary objective is to seamlessly integrate your product’s technology while prioritizing quality, efficiency, and regulatory adherence.
Cleaning verification
Douglas CDMO prioritizes process control and contamination prevention through rigorous analytical cleaning method development and process cleaning development.
These services are critical for maintaining a controlled and sterile environment necessary to produce pharmaceutical products. Douglas CDMO strictly adheres to Good Manufacturing Practice (cGMP) standards and guidelines set by regulatory authorities such as the FDA. Our commitment to maintaining a controlled manufacturing environment ensures that products meet the highest quality standards throughout the manufacturing process.