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Dr.
Ternik is Senior Research Advisor, Synthetic Molecule Design and Development at
Eli Lilly and Company in Indianapolis, IN. He is responsible for creating and
implementing patient centered design and drug delivery capability across
Lilly’s synthetic molecule drug product portfolio. Dr. Ternik received his bachelor’s
in Pharmacy from Butler University, Indianapolis, Indiana. After working as a
hospital pharmacist for the USVA and as a Research Pharmacist for Merrell Dow,
he attended to the University of Iowa and received his Ph.D. in Pharmaceutics.
Upon completion of his graduate studies, Dr. Ternik worked for Janssen
Pharmaceuticals before joining Eli Lilly in 1997. He has contributed to Lilly
in both scientific and management roles in Product Research and Development,
including 7 years as the Director of Formulation and Process Development. He
has significant experience in formulation development and manufacturing process
scale up and tech transfer. Dr. Ternik has led and overseen the development
more than 40 pivotal clinical and commercial formulations. He has experience
and expertise in oral, parenteral and alternative dosage form development, with
a primary focus on oral products. In addition to his responsibilities in
advancing Lilly’s synthetic molecule portfolio,
Dr. Ternik is highly engaged in
the IQ Consortium Drug Product Leadership Group (DPLG). He was a co-founder and chair of the IQ’s
Pediatric Working Group under the DPLG and is a former chair of the DPLG. He sits on the Lilly Pediatric Steering
Committee and is actively engaged in both US and European based pediatric
product development consortia. Dr.
Ternik is a pharmaceutical industry representative on the Federal Task Force on
Research Specific to Pregnant Women and Lactating Women (PRGLAC) through HHS
and the NICHD. He was also recently
appointed to the Dean’s Advisory Council for the College of Pharmacy and Health
Sciences at Butler University. He has
expertise in and has published on product development for special patient
populations, such as pediatrics and geriatrics. He is an active advocate for,
and leader in, advancing Lilly’s capability in product design, with focus on
addressing unmet patient needs through human-centered design.
Professor Hannah Batchelor is a
pharmaceutical scientist who has worked in academia, the NHS and within
pharmaceutical industry. She is currently based at the Strathclyde Institute of
Pharmacy and Biomedical Science, University of Strathclyde in Glasgow.
She works on the design and
manipulation of medicines to create age appropriate drug formulations to
maximise clinical efficacy in paediatric patients. Her research interests lie
in the optimisation of drug formulations to maximise their biopharmaceutical
performance and acceptability to children. Her research is informed by the
views of children, young people and parents to ensure that the patients are at
the centre of new developments.
Hannah is recognised as an expert
in biopharmaceutics and leads the Academy of Pharmaceutical Scientists Focus
group on biopharmaceutics in the UK as well as the European Paediatric
Formulation Initiative’s biopharmaceutics workstream. She is also an active
member of the Understanding paediatric gastrointestinal processes (UNGAP) consortium.
She has ongoing research projects that explore paediatric biopharmaceutics in
conjunction with Janssen; Certara; the FDA and GlaxoSmithKline.