Our Services

Discover how our local expertise, deep insights and curated connections can help you navigate the complex life sciences sector in Australia and New Zealand.

We partner with investors, start-ups, government and not-for-profits, designing and delivering outcomes tailored to your individual requirements.

Partner with us to accelerate your next project.

Strategy

Product Development

Strategic advice on R&D, Translation and Commercialisation in Australia and New Zealand to investors, entrepreneurs and start-ups across medical devices, diagnostics, pharmaceutical, and biotechnology.

Investment

Life sciences expertise to private equity and other investors.

Policy & Industry Engagement

Commercial insights and advice on strategic partnerships to government, academia and not-for profits.

Translation

First-in-Human Clinical Trial Specialist

Expert understanding of Australia's Phase I sector including public and private early phase trial providers across medical devices, diagnostics, pharmaceutical and biotechnology.

Services Providers

Identification, selection and qualification of pre-clinical labs, CROs, CDMOs, analytical labs, SMOs, public health sites, clinical trial networks, study coordinator services, recruitment services and patient advocacy groups. Leverage our expertise to get the best out of the RFP and bid-defence process for your clinical trial.

Study Design & Scientific Writing

Protocols, Clinical Investigation Plans, Investigator Brochures, Instructions for Use, Participant Informed Consent Forms. We create documents that fit the local environment and support timely local regulatory, ethics and governance approvals.

Trial Registration

Strategic advice on registration - know when and where to register your research and how to the use the wealth of information on registration platforms to your advantage.

Regulatory

Submission and management CTN or CTA with Australia's regulatory agency, the Therapeutic Goods Administration (TGA).

Trial Start Up

Strategic advice on Australia's ethics and governance system - which committees you should use to get the best outcome for your trial. Preparation of human research ethics submissions and research governance documentation. Advice on budgets, contracts, indemnity and insurance arrangements.

Trial Project Management

On the ground, experienced oversight of trial execution. Whether you're a local company looking to outsource your trial staffing or an off-shore seeking a local presence, we can manage your trial delivery, vendors, and sites.

Trial Rescue

Addressing recruitment challenges or seamlessly transferring to an alternate CRO or other service provider for the successful delivery of your trial.

Compliance

Ensure your clinical development program complies with Australian regulations and guidelines including Therapeutic Goods Administration, National Health and Medical Research Council, and various State legislation and requirements. Undertake Sponsor audits of service providers and sites.

Participant Engagement

Preparation of recruitment plans, engagement of recruitment services providers, and involvement of patient advocacy groups.

COMMERCIALISATION

Advisory Board

Knowledge, experience, critical thinking and analysis to start-ups and SMEs.

Technical Due Diligence

Expertise on health-related services and products to investors and incubator programs.

Start-Ups

Clinical development and commercialisation plans, pitch packs and grant writing to entrepreneurs seeking to access non-dilutive and dilutive funding and translate their technologies to investible assets.

Connection

Curated access to a network of trusted specialists in company creation, business advisory, intellectual property, health technology assessment, market access, medical affairs and regulatory affairs.

Services provided by Innoveren may be eligible for the Australian R&D tax incentive.