With over 30 years of experience, Ms. Danielle Giroud is an internationally recognized clinical research and regulatory expert within the global medical device industry. She has shared her extensive knowledge and experience with multi-national companies, organizations, and start-ups from around the world to help bring their products to market quickly and efficiently.
Ms. Giroud is also known for her contribution and engagement as founder and senior faculty board member of the World Medical Device Organization (WMDO), as well as convener for the expert group on clinical investigations (TC 194 WG4) for the ISO 14155, and liaison with the EU Commission - Clinical Investigation and Evaluation (CIE) task force and other regulatory authorities throughout the world.
Tan Hwee Ee
Senior Consultant Asia, Regulatory & Quality Assurance
Ms. Tan has more than 20 years of experience in the medical device industry as a consultant, engineer, and senior manager. As an international expert in global regulatory compliance systems including 21 CFR part 820, ISO 13485, and Asia GDMP, she has successfully achieved numerous product certifications for clients from all over the world and accompanies your product development for market access throughout Asia, US, and Europe.
Ms. Tan has a wealth of regulatory and quality assurance expertise that she translates into comprehensive training courses whether in-house, online or at seminars. She is also a member of Working Group 6 (WG6) of the Asian Harmonization Working Party (AHWP).
As a highly experienced financial management professional, Ms. Larpin holds a master’s degree in international finance as well as a master’s degree in international business administration.
Her dedication and knowledgeable skills in financial controlling and consolidating international financial projections for our different legal entities throughout the world make her a vital asset to the MD-Clinicals team.
Deputy Manager Clinical Department
Registered nurse, specialised in cardiology, with vast experience in clinical research of over 15 years in various positions in the medical device CRO industry.
MD-CLINICALS has a seamless collaboration with Brandwood CKC complementing our clinical/regulatory services with high level pre-clinical and specialised regulatory and quality assurance input. Brandwood CKC has a global reputation for excellence in regulatory, quality systems and commercialisation consultancy earned through service to international health innovators for more than 20 years. Headquartered in Sydney with international offices in Los Angeles, Wellington, Beijing, Taipei and Hong Kong with European Representation in Lonay, Switzerland. Brandwood CKC’s multilingual team brings decades of experience and deep technical competencies to a shared commercial focus and global market view. A trusted partner positioned to deliver comprehensive support across all areas of therapeutics and diagnostics in major international markets.