Comprehensive Contract Manufacturing (CMO) and Development (CDMO) services, offering tailored solutions for pharmaceutical development and manufacturing needs.
Efficient preparation of Drug Master Files (DMF), Chemistry, Manufacturing, and Controls (CMC), and Site Master Files (SMF) for regulatory compliance.
Conducting thorough pre-audits and audits to ensure regulatory compliance and adherence to quality standards in pharmaceutical processes.
Accurate translation services for pharmaceutical documents and audit reports, facilitating seamless communication in the global regulatory landscape.
