Archives: Speakers

Proficient clinical research/medical affairs professional with demonstrated success in a multitude of roles across numerous therapeutic areas and study phase in the US, Canada, APAC and EMEA. Provider of high quality independent consulting services to Medical Device, Biotechnology, and Pharmaceutical clients in support of study start-up, ongoing, rescue, and close out activities of clinical trials in all phases.

Paul van Meurs, MD, is currently the Director of Medical & Scientific Affairs, Oncology and is responsible for the oversight of Clario’s medical imaging and specialty solutions. Dr. Muers is a qualified MD with more than 20 years of experience in clinical development within the pharmaceutical industry. He has previous experience at BiOrion as their Chief Business Officer as well as Keosys Medical Imaging and Julius Clinical where he was responsible for business development activities. He is also the editor of the Dutch Textbook of Pharmaceutical Medicine (Published 2014).

Jaldip Vyas, QA Manager & Lead- Clinical trials & Pharmacovigilance- Audits, quality & compliance Mr. Jaldip Vyas is M.Pharm in Pharmacology & a QA specialist & lead at Alkem Laboratories Ltd. He has over 13 + years of QA auditing experience in the clinical research & Pharmacovigilance fields. Mr. Jaldip Vyas is currently responsible to perform audits for global pharmacovigilance (PV) & clinical trial (CT) activities at Alkem. Mr. Jaldip Vyas has broad experience in conducting various audits globally such as GCP investigator site audits, vendor audits, process audits, system audits, project audits, TMF audits, develop & implement strategic, tactical & operational level audit strategy in PV, mock inspection audits and establishing systems and processes for clinical trials & PV.

Graduated from Seoul National University College of Medicine M.D. in Internal Medicine Training in Hematology/Medical Oncology Industry experiences of 15 years : Pfizer, Samsung Bioepis, Crystal Genomics, Handok, Interpark Bio Convergence and Bridge Biotherapeutics Inc. Currently, CMO and Head of Oncology at Bridge Biotherapeutics Inc.

Katarzyna Moscicka is Global Head of PSI’s Feasibility Department and has been with PSI since 2008. She is a pharmacist by training She is a valued and experienced team member having undertaken +1,800 feasibility assessments and site identification activities in the last 14 years. Kasia has spearheaded the development of PSI’s feasibility methodology and processes, while at the same time overseeing the majority of PSI’s feasibility studies – many of which are in oncology, hematology or GI indications. In addition to being involved in feasibility department and company-wide initiatives, Kasia has recently worked together with other members of the PSI team to develop, test, and implement a new machine-learning feasibility platform. This tool will revolutionize the way enrolment scenarios are planned and executed. Kasia holds an MSc in Pharmacy and is based in Warsaw, Poland

As Head of Marketing & Communications at Double Dutch, Anna leads the cross-channel marketing plans for Double Dutch in the UK and supports the brand globally across export markets. Anna has worked in the drinks industry for the last 10 years, across the Atom Group (Master of Malt, Atom Brands & Maverick Drinks) as well as the IWSC and its portfolio of whisky events.

Having spent the previous 4 years at Brewdog managing one half of their UK Grocery division and prior to that in various buying roles at both Iceland and ASDA, I joined Double Dutch 6 months ago as Head of Retail. Leading and implementing the strategy across; UK Grocery, Ecommerce, UK Convenience/Wholesale and Premium Retail.

Passionate about shaping and delivering the R&D+i strategy to help Cork Supply succeed in long-term growth. Interested in prioritizing innovative ideas and embracing cross-functional challenges for go-to-market success. An expert in cork and bottle-wine-cork interactions, including aspects concerning food safety – European Regulation and FDA premises. A member of the Sustainability Committee at Cork Supply, particularly involved in assuring that sustainability goes beyond the environmental perception, for both the company and products. Ana Cristina is also a co-author in five patent families, has written numerous scientific publications in peer reviewed magazines and is active in technical committees such as ISO and CETIE.