Dor Pharmaceutical Services provides a broad range of proven, certified Qualified Person (QP) and Quality Assurance (QA) services

More Services

Qualified Person (QP)

Providing qualified person (QP) certification, outsourcing and insourcing, including batch release services.


Ongoing management of the quality system in accordance with the requirements of the Ministry of Health with constant readiness for review


Independent third-party audits, Comprehensive audit reports, Statements of compliance with GDP quality standards, Qualified, Regular audit report updates and re-auditing, GMP/GDP compliance programs.


Creating quality agreements / technical agreements with suppliers.

Establishing and maintaining quality systems

Establishing and maintaining quality systems to meet local regulations (importer license) and international pharmaceutical standards (GMP and GDP)


Developing and maintaining standard operating procedures (SOP)


Conducting pharmacovigilance and device vigilance activities, Providing medical information to caregivers and patients


Training teams and writing documentation, Managing complaints and contacts.

Clinical Trilas

Performing clinical trial quality assurance

Why Us?


Expertise and our deep familiarity with regulatory requirements and registration procedures of the Ministry of Health that helps compliance and regulation, improves quality and accelerates the ready products.


Our staff are professionals in the pharmaceutical and medical industry focused on client goals.

Effective training

DOR empowers customer staff with effective training and ongoing knowledge transfer, as well as information updates on emerging industry and regulatory changes.

Cost savings and flexibility

Accessing services as needed, empowering companies and helping them complete tasks that would otherwise be too expensive to perform.