Architectural, Engineering, GMP, QA and Validation Services
PharmOut offers a range of Architectural, Engineering, GMP, QA and Validation services to the Medicinal Cannabis, Medical Device, Pharmaceutical and Veterinary manufacturing industries so that they can meet the required relevant regulatory standards. PharmOut also has a proven track record of delivering successful projects for the cannabis, food, dairy and cosmetics manufacturing industries and can offer expertise on a fee for service basis or a fixed price basis. More recently PharmOut has been recognised as one of the worlds leading cannabis consulting firms.
PharmOut staff frequently share their knowledge in blogs.
Auditing Services
Our auditing options cover GMP Compliance, Regulatory Inspections and Post-Audit Remediation Programs – all to TGA, FDA and EMEA standards.
Continuous Improvement Consulting Services
PharmOut can show you how to apply processes such as Lean Manufacturing and Six Sigma within the regulatory constraints of the Pharma industry.
GMP Contractors
If you are resource-poor and need experienced, professional GMP contractors to get a job done, we can supply contractors with a range of GMP skills and knowledge.
GMP Consulting Services
We provide GMP consulting services that are based on relevant, cost-effective and practical compliance – not just compliance without regard to business demands!
GMP Technical Writers
Our GMP technical writing team is carefully recruited to not only provide you with an experienced technical writer but a writer who also brings GMP consulting strength to your project.
Healthcare and GMP Facility Design
PharmOut can deliver a GMP facility design that is not only compliant but also streamlines your manufacturing processes and includes Lean and World Class manufacturing concepts.
Medicinal Cannabis Growing and Facility Design Consulting
As a leading medicinal cannabis consulting company, and recognised as a leading cannabis grow consulting practice, we can deliver a complete medicinal cannabis facility design from the strain selection, propagation, growing (vegetative and flowering), to extraction, and of course the conventional dosage forms.
GMP Technical Writers
Our GMP technical writing team is carefully recruited to not only provide you with an experienced technical writer but a writer who also brings GMP consulting strength to your project.
Interim QA Managers and GMP Staff
If you’re resource poor we can help you finding temporary or permanent staff with specific technical skills and experience to support your manufacturing and site activities.
Pharma 4.0 Consultants
Our Pharma 4.0 consultants can help with your Industry 4.0 initiatives in Big Data, Additive Manufacturing and the Industrial Internet of Things (IIot), all referred to as Industry 4.0.
Pharmaceutical and GMP Consulting Engineers
Our Engineers like to get a strong grasp of your pharmaceutical processes before they start designing in order to avoid shoe-horning a process into a suboptimal building.
Project Management
We offer project management services that can help you get from the initial idea all the way to commencing production while complying with the required regulations.
TGA Regulatory Affairs Consultants
We can offer registration strategies and assistance to companies who wish to supply products to the Australian market but are unfamiliar with the regulatory requirements.
Validation Services
Our engineers offer a wide range of validation services that cover cleaning and process validation all the way to SharePoint and computer systems validation.