共同开辟一条通往人类繁荣和健康无处不在的未来之路
我们的专业和多元化团队融合了临床开发和监管事务管理方面的专业技能,以提高我们的合作伙伴将其疗法和设备推向市场的能力。
凭借从全球数百项批准中获得的深刻见解和知识,我们与您密切合作,为您的产品和人类健康设想最佳的最终状态。我们不仅关注静态的分阶段要求,还会探索加快市场认可的步骤,并探讨产品的未来发展。然后,我们精心制作 “反向旅程地图”,共同阐明通往那里的最佳途径。
我们完全遵守国际准则和现代法规,确保最高的服务质量。我们的团队以敏捷、协作、透明和高效的方式工作,从大局的角度优先考虑灵活性和包容性。
我们的共同目标是通过专注于改善合作伙伴和患者的预后,加速人类的健康和福祉。
我们的领导团队

With extensive global experience in the pharmaceutical and biotech industries, Mathew brings his sharp strategic insight into industry advancements coupled with a strong track record in the execution of clinical programs to facilitate the development, licensing and commercialisation of new medical and healthcare assets.
He has over 30 years’ experience in clinical research organisations (CROs) in therapeutics and operations supporting the rapid development of products and services. With a strong background in finance, budgeting and corporate governance, Mathew is an expert in forecasting and executive reporting. He uncovers innovative pathways to success through strategic advisory, implementing new systems and streamlining processes to maximise asset value for CROs, biotech and pharma companies.

Chris is an Australian educated and trained registered medical doctor with 15+ years of corporate pharmaceutical and clinical research experience in Australia and New Zealand.
His experience as a Phase 1 co-investigator in healthy volunteer and patient studies and as sponsor medical lead for clinical trials in diverse oncology, haematology and rare diseases allows him to quickly assess and influence the therapeutic area landscape on a peer-to-peer level with specialist doctors and bring this expertise internally to inform trial strategy and drive success with clinical trials.
He brings broad leadership experience and is a strong advocate for positively influencing a company’s culture through enterprise leadership, mentoring and deep passion for science.

With 10 years of experience in the pharmaceutical industry and regulatory affairs across AU, NZ and LATAM, Daniela leads global product approvals with expertise and precision. Her experience spans the registration of biological medicines, new chemical entities, generic medicines, medical devices, and orphan drugs. Daniela has worked with a variety of clients, from small biotech to large multinational pharmaceutical companies, adapting to their unique needs. She holds a BSc (Hons) in Pharmaceutical Chemistry and Pharmacy, and a Master’s in Cancer Sciences from The University of Melbourne. Passionate about technology, continuous learning, mentoring others, working in multicultural environments, and bringing new medicines and technologies to patients, Daniela is committed to advancing regulatory excellence and patient outcomes.
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