As a trusted global partner, we adhere strictly to international Good Manufacturing Practice (GMP) guidelines, ensuring the highest standards of quality, safety, and efficacy for every product we produce.

Our core competency lies in the complex and precise production of specialised softgel encapsulation and various liquid dosage forms for pharmaceutical classifications including oncology, dermatology, the central nervous system and immunity.

Douglas was proud to be named New Zealand Manufacturer of the Year in 2025.

Quality Assurance (QA) is the bedrock of our operations. Our integrated Quality Management System (QMS) governs every stage of the manufacturing life cycle, from raw material sourcing and formulation development to final packaging and release.

Our facilities are regularly audited and compliant with stringent global regulatory bodies, including the FDA, TGA, and our local regulatory standards.

We utilise advanced analytical instrumentation and rigorous in-process controls to maintain batch-to-batch consistency and purity.

All critical processes, equipment, and cleaning procedures are thoroughly validated to guarantee repeatable and reliable results, making us a dependable partner in contract manufacturing through Douglas CDMO.

Our scientists, technicians and analysts who work in our manufacturing facilities in Auckland are highly-qualified. Among our manufacturing employees is a rich depth of knowledge and intellectual competence in formulation, microbiology, process development and quality control procedures.