Rachel Di Leva is a dynamic, intuitive and commercially minded expert consultant, with over 24 years’ global experience in executive leadership, general management, regulatory compliance, product development, market access, risk management, policy and advocacy. Rachel has extensive expertise across all wellness product categories including nutraceuticals, complementary medicines, cosmetics & beauty products, foods, beverages and sports nutrition categories. Rachel has worked with some of the largest global health and wellness brands, including Swisse, Biostime, Arrotex, Caruso’s Natural Health, Boots and Holland & Barrett (UK).

Rachel holds a Bachelor Degree in Health Science (Naturopathy) with majors in Western Herbal Medicine and Nutrition, as well as a Post Graduate Diploma in Human Nutrition (Public Health major) and Masters of Science in Food Policy. Rachel has also completed the Leadership Development Program (Organisational Leadership) course with Melbourne Business School (University of Melbourne).

Rachel's strength lies in navigating the grey and being able to find commercially sound solutions to business challenges whether it be regulatory hurdles, formulation complications or navigating the best strategy for successful market entry.  

With 20 years of experience in regulatory and compliance, Kerry is passionate knowledgeable mentor and trainer, generous with knowledge gained heading regulatory departments in both cosmetic and therapeutic businesses in Australia. She has experienced working with local and international businesses as a consultant, as well as in-house, in FMCG, cosmetics, cosmeceuticals, foods, functional foods, and therapeutic supplements (listed medicines).

Kerry is highly experienced in all aspects of regulation and compliance in Australia, and experienced in successful Cosmetic PIF Registrations for both EU and China. Kerry has working expertise in all areas including registration submissions, product development, evidence packages, labelling, copy writing, advertising, claim substantiation, raw material and finished product manufacturing.

Kerry has written and delivered training regulatory modules to both local and international audiences.

"I really enjoy simplifying and stepping out regulatory frameworks and concepts to make them approachable and accessible for both seasoned industry professionals and those new to the industry. Regulations are always changing, so this field is never static. Anticipating challenges that businesses face to ensure compliance in an ever changing landscape, requires ongoing education".

Tina Bird is an accomplished professional with over 20 years’ experience in the pharmaceutical industry specialising in complementary and over-the-counter medicines. Tina’s expertise has been instrumental in leading companies including Blackmores, Catalent, and Bristol-Myers Squibb through intricate regulatory landscapes to bring innovative, high-quality products to global markets.

Tina is skilled at developing regulatory strategies for new product launches and customised processes for stringent TGA environments. Her skill set encompasses new product developments, specifications, evidence reviews, labelling, ARTG listings, product life-cycle management, advertising, eCTD dossiers, post-market surveillance, licences & permits for import/export, GMP clearances & quality systems, TGA audit, internal & supplier audits, and training programs.

With a Bachelor of Science in Microbiology/Pharmacology and a Graduate Certificate in Applied Microbiology & Biotechnology, Tina’s academic background is further enhanced by specialised training in management, project management, auditing, and risk management. Passionate about science and lifelong learning, Tina is dedicated to sharing her knowledge and insights with clients in Australia and around the world.

Melissa Cohen is an experienced Regulatory and Clinical Affairs Consultant with over 23 years of working in the medical device industry as both a consultant and in many managerial roles for various medical device manufacturers in Australia, UK, Europe and Israel.

Melissa has extensive experience in regulatory submissions for medical devices in global markets across a variety of medical fields including Gastroenterology, Orthopaedics, Ophthalmology, In-Vitro diagnostics, Physical Medicine and others.

Additionally, Melissa has worked in various roles across clinical affairs including the implementation and design of clinical investigations through to writing the final clinical report. She is skilled in writing technical documentation including technical files, Clinical Evaluation Reports, Periodic Safety Update Reports, Post-Market Clinical Follow-Up etc.). Melissa holds a BSc from Melbourne University and a Grad Dip in Business Management.

With a decade of experience in the cosmetic industry and a solid foundation in pharmaceutical science, Samantha Thomson is a highly regarded consultant specialising in skincare and haircare. Throughout her career, Samantha has successfully led R&D teams, driving innovative product development and formulation. Her work is characterised by a commitment to ensuring that every product meets the highest standards of quality and efficacy.

Samantha’s expertise extends across the Australian market and international exports, with a particular emphasis on EU regulations and the meticulous preparation of Product Information Files (PIFs). Her deep understanding of regulatory requirements and market dynamics positions her as a key resource for clients navigating the complex landscape of the cosmetic industry.

Samantha’s comprehensive knowledge and strategic insights make her an invaluable asset for companies aiming to innovate and succeed in a highly competitive market.