Scendea Presents: An Introduction & Best Practices Guide to Target Product Profiles
Webinar Description: Join Scendea’s Regulatory & Product Development experts for an insightful webinar introduction and best practices guide to Target Product Profiles (TTPs) covering:
What is a TPP?
The key components, application and use for a TPP
Conventional parameters in TPP criteria
Strategic considerations and best practices
About Scendea
Scendea is a leading product development and regulatory consulting group serving the pharmaceutical and biotechnology industry. Our international team offers strategic and operational support in the fields of quality/CMC, non-clinical/ toxicology, clinical/medical and regulatory, which guide products efficiently from early development to marketing approval. Scendea’s scientific excellence, industry experience, commercial awareness and a collaborative approach allow our expert team to solve complex issues associated with medicinal product development.
Meet the Speakers
Karen is a Principal Consultant at Scendea, responsible for providing nonclinical technical advice and product development strategies to our clients. Karen was formerly a Senior Nonclinical Assessor and Head of Nonclinical Assessment for Clinical Trials at the MHRA.
Karen has over 20 years’ experience in toxicology, having also previously worked for the NHS and Food Standards Agency. Karen holds a BSc (Hons) in Pharmacology and an MSc in Applied Toxicology.
Dr Caroline Keane is a Senior Consultant at Scendea with 20 years of experience working on both early and late-stage clinical programmes. Caroline has worked across a broad range of therapeutic areas including allergy and respiratory, Immunology, women’s health and oncology and haematology.
Caroline started her pharmaceutical career at Pfizer, working as a clinical development manager and was most recently a senior clinical scientist in oncology at Roche. Caroline holds a PhD in Immunology from University College Dublin.
