Exploring Common CDISC ADaM Dataset Conformance Findings
What you need to know when validating your CDISC ADAM datasets During the regulatory review…
Danielle Pillsbury2020年9月3日
The supplementary domain in SDTM: good, bad and ugly
All you need to know about the supplementary domain in SDTM The supplementary domain in…
Danielle Pillsbury2020年7月2日
Data Validation in Clinical Research: Confusing Rules Explained
What should you do when faced with confusing findings during data validation in clinical research? …
Danielle Pillsbury2020年4月30日
The Rare Disease Drug Dilemma: Great Value, High Price, Limited Access?
This webinar will explain how pricing has evolved for the rare disease drug market and…
webdev2020年2月19日
How to Demonstrate Virtual Bioequivalence for Complex Dermal Generic Drugs
This webinar will explain how Certara expanded its PBPK Simcyp Simulator to incorporate an extensive…
webdev2020年1月24日
How to Perform IVIVC for Delayed Release Drug Formulations
This webinar showed how to use a time correction factor to establish a meaningful IVIVC…
webdev2019年8月20日
Innovative Solutions for Fast-Tracking Drugs for Rare Diseases
This webinar discussed which pharmaceutical payer strategies work and which don't in our rapidly changing…
webdev2019年8月10日
Advanced Analytics Using RWD Mitigates Risks in AD Drug Development & Reimbursement
This webinar explained how advanced analytics using real-world data can mitigate challenges in Alzheimer’s disease…
webdev2019年5月13日
