Clean Room / Laboratory Engineers

Our engineers form part of a multidisciplinary team, experienced in product scale up, facility design, containment, operations, product registration and validation. We can work with your existing architect or general builders engineers to impart our specialist expertise in the following areas.

Hospital Laboratories

Our engineers can design and build hospital laboratories used for drug or research purposes where appropriate clean room designs are essential. Often these clinical research laboratories or units conducting first-in-human clinical studies of investigational medications on behalf of the world's leading pharmaceutical and biotechnology companies, need to comply with all international standards and the sponsor companies requirements. These exacting requirements are a distraction task for most researchers with more important priorities.

cGMP Laboratory

If materials are developed or processed for animal or human therapy in a cGMP laboratory, the laboratory must comply with exacting standards. Typically laboratories include sample receipt and shipping, histology, macro dissection, coding, staining, paraffin block storage, microscopy suites, and cryotomy laboratories and cryogenic storage facilities.

Tissue Processing and Banking Facility

Facility housing laboratories, clean rooms and cryogenic storage for harvesting, processing and banking of human tissue for surgical implantation must be compliant with TGA code of GMP for Blood and Tissue Products.

Radiation Imaging & Therapy Services

PharmOut has worked with a number of Australia's pre-eminent hospitals and facilities offering PET and other oncology radiation treatment and diagnostic imaging solutions; some have been at the clinical trial stage.

PharmOut can be retained as your GMP engineering consultant for master planning or design for your additions and renovations.

The Benefits

PharmOut's engineers will allow you to:

• gain greater knowledge of the GMP / quality issues affecting your project
• develop increased awareness of regulatory expectations
• recognise commonly seen GMP deficiencies and learn how to reduce them in your organisation
• receive guidance on changing legislation and increasing complexity regulatory landscape. 

More information

If you would like a quote or would like to ask questions, please contact us.