Kathleen LeGrow
Articles
Integrating CMC Document Preparation into the Development Process for Vaccine INDs
Rachel Thornton;Anna Hagen;Robert Sitrin;Tracy Janus;Kathleen LeGrow;Laura Howson;Anne Aunins;Robin Robinett
September 1st 2003Vaccine process development is complex, and so are the documents required before clinical trials begin. Technical writers and editors can effectively coordinate the timely authoring, reviewing, and auditing of regulatory documents, minimizing filing delays.
Latest Updated Articles
Published: September 11th 2024 | Updated: September 18th 2024
CPHI Pharma Award Finalists Announced for 2024
Published: March 27th 2024 | Updated: June 28th 2024
AbbVie Acquires Landos Biopharma and Gets Full FDA Nod for ADC Product
Published: December 9th 2024 | Updated: December 26th 2024
Recap Key Industry Trends for Viral Clearance and NGS
Published: December 7th 2024 | Updated: December 26th 2024
Enhancing Quality Through Training
Published: July 20th 2020 | Updated: December 26th 2024
Contact BioPharm International Editors
Published: July 19th 2020 | Updated: December 26th 2024
Editorial Information: BioPharm International Submission Guidelines and Editorial Calendars
