MaH
Clinical Trial
Solutions
We provide Secondary packaging and Primary & Secondary labelling
Our GMP facilities provide controlled ambient, cold chain and frozen storage areas
We offers comprehensive global logistics services for clinical trials across all phases
We handle the management of returned drug accountability and destruction for clinical trial
We provide consultation services for addressing clinical regulatory inquiries
ABOUT US
MaH are experts in the storage, distribution, labelling and packing of clinical trial materials in APAC and Global regions. Our GMP/GWP facility is designed to meet the needs of clinical trial sponsors, contract research organizations (CROs), and other vendors involved in the clinical trial supply chain.
Meet Our Quality Leader
Matthew Bugg
Global Quality Director - Clinical Trials Depot Mgt
Matthew has worked in the pharmaceutical industry for over 20 years starting off in the community pharmacy family business before moving into hospital pharmacy and then transitioning into the global pharmaceutical sector.
Having worked in leadership roles for some of the biggest pharma companies which includes, GSK, Roche, AstraZeneca and BeiGene, Matthew is seasoned in all relevant regulatory guidelines including, but not limited to, PIC/s, TGA, MHRA, CFDA, ICH, ISO, PDA and WHO.
Matthew also holds a (Pharmacy degree from Birkbeck University London UK) and a (Master’s Degree in Pharmaceutical Technology and Quality Assurance from Leeds School of Healthcare UK).
Prior to the industry Matthew worked in hospital pharmacies and gained several years’ experience compounding IV chemotherapy for clinical studies. Matthew has seen firsthand the positive impact of clinical trials with the advancements of novel medicines in the field of oncology medicine.
