Sponsors & Exhibitors

Interested in sponsoring, exhibiting or increasing your exhibitor profile by adding a company description, logo or website tile?

Sponsorship is now open! Download the order form here!

Major Sponsor

 

 

 

Exhibitors

Company	Company Details	Booth #
ARCS Australia	ARCS Australia Ltd (previously the Association of Regulatory and Clinical Scientists) is a professional development association for people working in the development of therapeutic goods. Founded in 1984, we now have approximately 2,500 members who are involved in regulatory affairs, clinical research, health economics, medical devices, diagnostics, medical devices, data management, statistics, medical writing, pharmacovigilance, and the provision of medical information in the Australian therapeutics industry.	15
Adriot People		12
BioPharmaceutical Solutions		17
GlaxoSmithKline		20
Hahn Healthcare		26
Hays		11
	The McCloud Group have over 20 years’ experience successfully working with many clinical and study teams at the global and regional level. Their expertise include: working as project and study biostatisticians, data managers, protocol development, health economics, training and much more. With a pragmatic approach and recognising the need to develop creative solutions to clinical trial design and sample size determinations, the MCG team is adept at balancing the scientific and budgetary requirements of clinical trials. As a world class Biometrics CRO servicing Australia, Asia Pacific, and beyond, MCG can deliver its extensive international industry experience to your clinical trial.	18
OnQ Recruitment		22
Pharmaceutical & Medical Professionals		16
PharmOut	PharmOut consults to the pharmaceutical and medical device industries on GMP compliance, drug registration, validation and the improvement of manufacturing processes. We also offer complete engineering design, compliance & project management services for GMP facilities. PharmOut’s consultants include international experts on GMP facility design and computer systems validation as well as ex-auditors from the TGA and PIC/S. Our specialisation is practical, cost-effective GMP compliance. We offer validation engineers who can write validation plans, specifications and qualification protocols for cleaning validation, equipment validation, computers systems validation, analytical method validation or process validation. Our TGA registration services are supported by a thorough knowledge of GMP (QA) and validation and are offered for drugs, devices and complementary medicines. Our technical document writers can help you create a Quality Management System, writing procedures and work instructions from scratch, or can bring your current system into compliance with TGA /FDA requirements. PharmOut’s experienced engineers can develop concept and detailed designs, around new or existing production processes. They will ensure full GMP compliance through careful project management and verification (validation). Finally, we offer on-site, classroom training and e-learning solutions on GMP compliance, validation and documentation writing.	21